The National Health Interview Survey (NHIS) is the principal source of information on the health of the civilian noninstitutionalized population of the United States and is one of the major data collection programs of the National Center for Health Statistics (NCHS) which is part of the Centers for Disease Control and Prevention (CDC). The National Health Survey Act of 1956 provided for a continuing survey and special studies to secure accurate and current statistical information on the amount, distribution, and effects of illness and disability in the United States and the services rendered for or because of such conditions. The survey referred to in the Act, now called the National Health Interview Survey, was initiated in July 1957. Since 1960, the survey has been conducted by NCHS, which was formed when the National Health Survey and the National Vital Statistics Division were combined. NHIS data are used widely throughout the Department of Health and Human Services (DHHS) to monitor trends in illness and disability and to track progress toward achieving national health objectives. The data are also used by the public health research community for epidemiologic and policy analysis of such timely issues as characterizing those with various health problems, determining barriers to accessing and using appropriate health care, and evaluating Federal health programs. The NHIS also has a central role in the ongoing integration of household surveys in DHHS. The designs of two major DHHS national household surveys have been or are linked to the NHIS. The National Survey of Family Growth used the NHIS sampling frame in its first five cycles and the Medical Expenditure Panel Survey currently uses half of the NHIS sampling frame. Other linkage includes linking NHIS data to death certificates in the National Death Index (NDI). While the NHIS has been conducted continuously since 1957, the content of the survey has been updated about every 10-15 years. In 1996, a substantially revised NHIS questionnaire began field testing. This revised questionnaire, described in detail below, was implemented in 1997 and has improved the ability of the NHIS to provide important health information.

Since 2013, the Robert Wood Johnson Foundation (RWJF) has led the development of a pioneering national action framework to advance a "culture that enables all in our diverse society to lead healthier lives now and for generations to come." Accomplishing these principles requires a national paradigm shift from a traditionally disease and health care-centric view of health toward one that focuses on well-being. Recognizing that paradigm shifts require intentional actions, RWJF worked with RAND researchers to design an actionable path to fulfill the Culture of Health (CoH) vision. A central piece of this work is the development of measures to assess constructs underlying a CoH. The National Survey of Health Attitudes is a survey that RWJF and RAND analysts developed and conducted as part of the foundation's CoH strategic framework. The foundation undertook this survey to measure key constructs that could not be measured in other data sources. Thus, the survey was not meant to capture the full action framework that informs CoH, but rather just selected measure areas. The questions in this survey primarily addressed the action area: making health a shared value. The survey covers a variety of topics, including views regarding what factors influence health, such as the notion of health interdependence (peer, family, neighborhood, and workplace drivers of health), values related to national and community investment for health and well-being; behaviors around health and well-being, including civic engagement on behalf of health, and the role of community engagement and sense of community in relation to health attitudes and values. This study includes the results from the 2018 RWJF National Survey of Health Attitudes. This 2018 survey is considered the second wave, the first wave of the survey was conducted in 2015 (ICPSR 37405). In 2018, the study team fielded an updated version that included many of the same questions but added some new constructs that were of interest as part of the larger Culture of Health effort. This study complements the overview of the 2015 survey described in the RAND report Development of the Robert Wood Johnson Foundation National Survey of Health Attitudes (Carman et al., 2016).

The basic purpose of the Health Interview Survey is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. There are five types of records in this core survey, each in a separate data file. The variables in the Household File (Part 1) include type of living quarters, size of family, number of families in household, and geographic region. The variables in the Person File (Part 2) include sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. These variables are found in the Condition, Doctor Visit, and Hospital Episode Files as well. The Person File also supplies data on height, weight, bed days, doctor visits, hospital stays, years at residence, and region variables. The Condition (Part 3), Doctor Visit (Part 4), and Hospital Episode (Part 5) Files contain information on each reported condition, two-week doctor visit, or hospitalization (twelve-month recall), respectively. A sixth, seventh, eighth, and ninth file have been added, along with the five core files. The Alcohol/Health Practices Supplement File (Part 6) includes information on diet, smoking and drinking habits, and health problems. The Bed Days and Dental Care Supplement File (Part 7) contains information on the number of bed days, the number of and reason for dental visits, treatment(s) received, type of dentist seen, and travel time for visit. The Doctor Services Supplement File (Part 8) supplies data on visits to doctors or other health professionals, reasons for visits, health conditions, and operations performed. The Health Insurance Supplement File (Part 9) documents basic demographic information along with medical coverage and health insurance plans, as well as differentiates between hospital, doctor visit, and surgical insurance coverage.

Abstract

The main objective of a demographic household survey (DHS) is to provide estimates of a number of basic demographic and health variables. This is done through interviews with a scientifically selected probability sample that is chosen from a well-defined population.

The 2007 Nauru Demographic and Health Survey (2007 NDHS) was one of four pilot demographic and health surveys conducted in the Pacific under an Asian Development Bank ADB/ Secretariat of the Pacific Community (SPC) Regional DHS Pilot Project. The primary objective of this survey was to provide up-to-date information for policy-makers, planners, researchers and programme managers, for use in planning, implementing, monitoring and evaluating population and health programmes within the country. The survey was intended to provide key estimates of Nauru's demographics and health situation. The findings of the 2007 NDHS are very important in measuring the achievements of family planning and other health programmes. To ensure better understanding and use of these data, the results of this survey should be widely disseminated at different planning levels. Different dissemination techniques will be used to reach different segments of society.

The primary purpose of the 2007 NDHS was to furnish policy-makers and planners with detailed information on fertility, family planning, infant and child mortality, maternal and child health, nutrition, and knowledge of HIV and AIDS and other sexually transmitted infections.

NOTE: The only dissemination used was wide distribution of the report. A planned data use workshop was not undertaken. Hence there is some misconceptions and lack of awareness on the results obtained from the survey. The report is provided on the NBOS website free for download.

Geographic coverage

National Coverage - Districts

Analysis unit

• Households
• Children (0-14yrs)
• Individual women of reproductive age (15-49 yrs)
• Individual men of reproductive age (15yrs+)
• Facilities providing reproductive and child health services

Universe

The survey covered all household members (usual residents), - All children (aged 0-14 years) resident in the household - All women of reproductive age (15-49 years) resident in all household - All males (15yrs and above) in every second household (approx. 50%) resident in selected household

Results: The 2007 Nauru Demographic Health Survey (2007 NDHS) is a nationally representative survey of 655 eligible women (aged 15-49) and 392 eligible men (aged 15 and above).

Kind of data

Sample survey data [ssd]

Sampling procedure

IDG NOTES: Locate sampling documentation with SPC (Graeme Brown) and internal files. Add in this sections. Or second option dilute appendix A Sampling and extract key issues.

ESTIMATES OF SAMPLING ERRORS - Refer to Appendix A of final NDHS2007 report or; - External Resources - 2007 DHS- Appendix A and B Sampling (to be created separatedly by IDG progress ongoing)

Sampling deviation

IDG NOTES: Locate sampling documentation with Macro and internal files. Add in this section. Or second option dilute appendix B Sampling and extract key issues.

ESTIMATES OF SAMPLING ERRORS - Refer to Appendix B of final NDHS2007 report or;

• External Resources
  • 2007 DHS- Appendix A and B Sampling (to be created separatedly by IDG progress ongoing)

Extract:

In the 2007 NDHS Report of the survey results, sampling errors for selected variables have been presented in a tabular format. The sampling error tables should include:

.. Variable name

R: Value of the estimate; SE: Sampling error of the estimate; N: Unweighted number of cases on which the estimate is based; WN: Weighted number of cases; DEFT: Design effect value that compensates for the loss of precision that results from using cluster rather than simple random sampling; SE/R: Relative standard error (i.e. ratio of the sampling error to the value estimate); R-2SE: Lower limit of the 95% confidence interval; R+2SE: Upper limit of the 95% confidence interval (never >1.000 for a proportion).

Mode of data collection

Face-to-face [f2f]

Research instrument

DHS questionnaire for women cover the following sections:

• Background characteristics (age, education, religion, etc)
• Reproductive history
• Knowledge and use of contraception methods
• Antenatal care, delivery care and postnatal care
• Breastfeeding and infant feeding
• Immunization, child health and nutrition
• Marriage and recent sexual activity
• Fertility preferences
• Knowledge about HIV/AIDS and other sexually transmitted infections
• Husbands background and women's work

The men's questionnaire covers the same except for sections 4, 5, 6 which are not applicable to men.

It was also recognized that some countries have a need for special information that is not contained in the core questionnaire. Separate questionnaire modules were developed on a series of topics. These topics are optional and include:

• maternal mortality
• pill-taking behaviour
• sterilization experience
• children's education
• women's status
• domestic violence
• health expenditures
• consanguinity

The Papua New Guinea (PNG) questionnaire was proposed for Nauru to adapt as in comparison to the existing DHS model, this is not as lengthy and time-consuming. The PNG questionnaire also dealt with high incidence of alcohol and tobacco in Nauru. Questions on HIV/AIDS and STI knowledge were included in the men's questionnaire where it was not included in the PNG questionnaire.

Response rate

IDG NOTES: Locate response rate documentation with SPC (Graeme Brown) and internal files. Add in this sections.

Student Mental Health Survey

Key aspects covered in the dataset include:

• Demographic details such as gender, age, and university.
• Academic details like degree level, major, academic year, and current CGPA.
• Student's residential status and experiences with discrimination, harassment, or bullying on campus.
• Student's lifestyle factors include frequency of sports engagement and average sleep hours per night.
• Student's satisfaction with their field of study and their perception of academic workload.
• Addressing the academic pressure, financial concerns, and the quality of social relationships on campus.
• Frequency of experiencing depression, anxiety, feelings of isolation, and insecurity about the future.
• Activities that students engage in to relieve stress.

This dataset is valuable for researchers, and policymakers interested in student well-being, mental health, and academic success.

The World Health Survey was implemented by WHO in 2002–2004 in partnership with 70 countries to generate information on the health of adult populations and health systems. The total sample size in these cross-sectional studies includes over 300,000 individuals. Survey materials and data are available through the WHO World Health Survey Data Archive accessible from the WHS webpage. (From the WHO World Health Survey webpage).

The National Health Survey of Spain 2017 (ENSE 2017), carried out by the Ministry of Health, Consumption and Social Welfare with the collaboration of the National Institute of Statistics, collects health information related to the population residing in Spain in 23,860 households. It is a five-yearly survey that allows knowing numerous aspects of the health of citizens at a national and regional level, and planning and evaluating actions in health matters. It consists of 3 questionnaires, household, adult and minor, which address 4 large areas: sociodemographic, health status, use of health services and health determinants.

Abstract

The 2023 Jordan Population and Family Health Survey (JPFHS) is the eighth Population and Family Health Survey conducted in Jordan, following those conducted in 1990, 1997, 2002, 2007, 2009, 2012, and 2017–18. It was implemented by the Department of Statistics (DoS) at the request of the Ministry of Health (MoH).

The primary objective of the 2023 JPFHS is to provide up-to-date estimates of key demographic and health indicators. Specifically, the 2023 JPFHS: • Collected data at the national level that allowed calculation of key demographic indicators • Explored the direct and indirect factors that determine levels of and trends in fertility and childhood mortality • Measured contraceptive knowledge and practice • Collected data on key aspects of family health, including immunisation coverage among children, prevalence and treatment of diarrhoea and other diseases among children under age 5, and maternity care indicators such as antenatal visits and assistance at delivery • Obtained data on child feeding practices, including breastfeeding, and conducted anthropometric measurements to assess the nutritional status of children under age 5 and women age 15–49 • Conducted haemoglobin testing with eligible children age 6–59 months and women age 15–49 to gather information on the prevalence of anaemia • Collected data on women’s and men’s knowledge and attitudes regarding sexually transmitted infections and HIV/AIDS • Obtained data on women’s experience of emotional, physical, and sexual violence • Gathered data on disability among household members

The information collected through the 2023 JPFHS is intended to assist policymakers and programme managers in evaluating and designing programmes and strategies for improving the health of the country’s population. The survey also provides indicators relevant to the Sustainable Development Goals (SDGs) for Jordan.

Geographic coverage

National coverage

Analysis unit

• Household
• Individual
• Children age 0-5
• Woman age 15-49
• Man age 15-59

Universe

The survey covered all de jure household members (usual residents), all women aged 15-49, men aged 15-59, and all children aged 0-4 resident in the household.

Kind of data

Sample survey data [ssd]

Sampling procedure

The sampling frame used for the 2023 JPFHS was the 2015 Jordan Population and Housing Census (JPHC) frame. The survey was designed to produce representative results for the country as a whole, for urban and rural areas separately, for each of the country’s 12 governorates, and for four nationality domains: the Jordanian population, the Syrian population living in refugee camps, the Syrian population living outside of camps, and the population of other nationalities. Each of the 12 governorates is subdivided into districts, each district into subdistricts, each subdistrict into localities, and each locality into areas and subareas. In addition to these administrative units, during the 2015 JPHC each subarea was divided into convenient area units called census blocks. An electronic file of a complete list of all of the census blocks is available from DoS. The list contains census information on households, populations, geographical locations, and socioeconomic characteristics of each block. Based on this list, census blocks were regrouped to form a general statistical unit of moderate size, called a cluster, which is widely used in various surveys as the primary sampling unit (PSU). The sample clusters for the 2023 JPFHS were selected from the frame of cluster units provided by the DoS.

The sample for the 2023 JPFHS was a stratified sample selected in two stages from the 2015 census frame. Stratification was achieved by separating each governorate into urban and rural areas. In addition, the Syrian refugee camps in Zarqa and Mafraq each formed a special sampling stratum. In total, 26 sampling strata were constructed. Samples were selected independently in each sampling stratum, through a twostage selection process, according to the sample allocation. Before the sample selection, the sampling frame was sorted by district and subdistrict within each sampling stratum. By using a probability proportional to size selection at the first stage of sampling, an implicit stratification and proportional allocation were achieved at each of the lower administrative levels.

For further details on sample design, see APPENDIX A of the final report.

Mode of data collection

Computer Assisted Personal Interview [capi]

Research instrument

Five questionnaires were used for the 2023 JPFHS: (1) the Household Questionnaire, (2) the Woman’s Questionnaire, (3) the Man’s Questionnaire, (4) the Biomarker Questionnaire, and (5) the Fieldworker Questionnaire. The questionnaires, based on The DHS Program’s model questionnaires, were adapted to reflect the population and health issues relevant to Jordan. Input was solicited from various stakeholders representing government ministries and agencies, nongovernmental organisations, and international donors. After all questionnaires were finalised in English, they were translated into Arabic.

Cleaning operations

All electronic data files for the 2023 JPFHS were transferred via SynCloud to the DoS central office in Amman, where they were stored on a password-protected computer. The data processing operation included secondary editing, which required resolution of computer-identified inconsistencies and coding of open-ended questions. Data editing was accomplished using CSPro software. During the duration of fieldwork, tables were generated to check various data quality parameters, and specific feedback was given to the teams to improve performance. Secondary editing and data processing were initiated in July and completed in September 2023.

Response rate

A total of 20,054 households were selected for the sample, of which 19,809 were occupied. Of the occupied households, 19,475 were successfully interviewed, yielding a response rate of 98%.

In the interviewed households, 13,020 eligible women age 15–49 were identified for individual interviews; interviews were completed with 12,595 women, yielding a response rate of 97%. In the subsample of households selected for the male survey, 6,506 men age 15–59 were identified as eligible for individual interviews and 5,873 were successfully interviewed, yielding a response rate of 90%.

Sampling error estimates

The estimates from a sample survey are affected by two types of errors: nonsampling errors and sampling errors. Nonsampling errors are the results of mistakes made in implementing data collection and in data processing, such as failure to locate and interview the correct household, misunderstanding of the questions on the part of either the interviewer or the respondent, and data entry errors. Although numerous efforts were made during the implementation of the 2023 Jordan Population and Family Health Survey (2023 JPFHS) to minimise this type of error, nonsampling errors are impossible to avoid and difficult to evaluate statistically.

Sampling errors, on the other hand, can be evaluated statistically. The sample of respondents selected in the 2023 JPFHS is only one of many samples that could have been selected from the same population, using the same design and sample size. Each of these samples would yield results that differ somewhat from the results of the actual sample selected. Sampling errors are a measure of the variability among all possible samples. Although the degree of variability is not known exactly, it can be estimated from the survey results.

Sampling error is usually measured in terms of the standard error for a particular statistic (mean, percentage, etc.), which is the square root of the variance. The standard error can be used to calculate confidence intervals within which the true value for the population can reasonably be assumed to fall. For example, for any given statistic calculated from a sample survey, the value of that statistic will fall within a range of plus or minus two times the standard error of that statistic in 95% of all possible samples of identical size and design.

If the sample of respondents had been selected by simple random sampling, it would have been possible to use straightforward formulas for calculating sampling errors. However, the 2023 JPFHS sample was the result of a multistage stratified design, and, consequently, it was necessary to use more complex formulas. Sampling errors are computed using SAS programs developed by ICF. These programs use the Taylor linearisation method to estimate variances for survey estimates that are means, proportions, or ratios. The Jackknife repeated replication method is used for variance estimation of more complex statistics such as fertility and mortality rates.

A more detailed description of estimates of sampling errors are presented in APPENDIX B of the survey report.

Data appraisal

Data Quality Tables

• Household age distribution
• Age distribution of eligible and interviewed women
• Age distribution of eligible and interviewed men
• Age displacement at age 14/15
• Age displacement at age 49/50
• Pregnancy outcomes by years preceding the survey
• Completeness of reporting
• Standardization exercise results from anthropometry training
• Height and weight data completeness and quality for children
• Height measurements from random subsample of measured children
• Interference in height and weight measurements of children
• Interference in height and weight measurements of women
• Heaping in

The National Survey of Children’s Health (NSCH) is sponsored by the Maternal and Child Health Bureau of the Health Resources and Services Administration, an Agency in the U.S. Department of Health and Human Services.The NSCH examines the physical and emotional health of children ages 0-17 years of age. Special emphasis is placed on factors related to the well-being of children. These factors include access to - and quality of - health care, family interactions, parental health, neighborhood characteristics, as well as school and after-school experiences.The NSCH is also designed to assess the prevalence and impact of special health care needs among children in the US and explores the extent to which children with special health care needs (CSHCN) have medical homes, adequate health insurance, access to needed services, and adequate care coordination. Other topics may include functional difficulties, transition services, shared decision-making, and satisfaction with care. Information is collected from parents or caregivers who know about the child's health.

In a Health Examination Survey (HES) objective health information is collected among a representative sample of the total population, including those who have no contact with health services. The collection of objective health measures at population level is particularly important for items that are often not accurately reported in a health interview survey (e.g. height and weight) and for diseases that may be present without any symptoms but have important health consequences (e.g. high blood pressure or high cholesterol level in the blood). The data from HES are essential for solid health policy development based on the population’s needs.

In 2018 the sixth Belgian Health Interview Survey (HIS) was organised by Sciensano. Information on the health status, lifestyle, health care use and socio-demographic characteristics were collected among a representative sample of 11.300 people residing in Belgium. From March 1st 2018 onwards, eligible HIS participants were invited to participate also in a HES. Respondents were eligible if they are at least 18 years and had participated in the HIS themselves (no proxy interview). About 1.100 respondents agreed to participate; they were visited at home by a trained nurse.

The HES included a short additional questionnaire, a physical examination and the collection of a blood sample. The physical examination consisted of the measurement of height, weight, waist circumference and blood pressure. Laboratory blood analyses included the measurement of glucose and cholesterol in the blood. The results were transferred to Sciensano in a coded way, ensuring that participants could not be identified. Through a unique identification code it is possible to link the HES data with information from the same people that was obtained in the HIS.

The Public Health Agency of Sweden annually conducts a national public health survey, Health on Equal Terms, including a sample of 20 000 people aged 16-84 years. The survey, which was conducted for the first time in 2004, is an on going collaboration between the The Public Health Agency of Sweden and county councils/regions in Sweden and is carried out with help from Statistics Sweden (SCB). All studies, since 2004, can be found under the tab Related studies.

The survey is voluntary and done with the purpose to investigate the health in the population and to show changes in the population's health over time as a follow up of the national health politics.

The sample is randomly drawn from the Statistics Sweden's population register and includes 20 000 people aged 16-84 years. The personal data is confidential and protected by law and those working with this survey are obliged to practice professional secrecy. Individual answers can not be identified in the results.

The study participants are since 2007 given the opportunity to answer the survey on the web. Since 2012, the web survey is also in English, and since 2014 also in Finnish.

The questionnaire includes about 85 questions. Each county council has its own introduction letter and the questions has been prepared in collaboration with representatives from a number of different community medicine units. The origin and quality of the questions are described in the report "Objective and background of the questions in the national public health survey". Most questions recur each year, but questions can in particular cases be replaced by other questions of good quality and national relevance.

The questions in the national public health survey cover physical and mental health, consumption of pharmaceuticals, contact with healthcare services, dental health, living habits, financial conditions, work and occupation, work environment, safety and social relationships. Data regarding education is collected from the education register, and data of income, economic support, sickness benefits and pensions from the income an taxation register.

Purpose:

The aim is to investigate the health in the population and to show changes in the population's health over time as a follow up of the national health politics.

As part of the Detroit Community Health Assessment (CHA) process, the Health Department and community partners worked with the University of Michigan Detroit Metropolitan Area Communities Study (DMACS) team to conduct a representative citywide survey of 1,216 residents to gather relevant information about Detroiters’ experiences, perceptions, priorities and aspirations around community health. The survey was implemented in the summer of 2018 and the results of the survey are included here.

Abstract

Different countries have different health outcomes that are in part due to the way respective health systems perform. Regardless of the type of health system, individuals will have health and non-health expectations in terms of how the institution responds to their needs. In many countries, however, health systems do not perform effectively and this is in part due to lack of information on health system performance, and on the different service providers.

The aim of the WHO World Health Survey is to provide empirical data to the national health information systems so that there is a better monitoring of health of the people, responsiveness of health systems and measurement of health-related parameters.

The overall aims of the survey is to examine the way populations report their health, understand how people value health states, measure the performance of health systems in relation to responsiveness and gather information on modes and extents of payment for health encounters through a nationally representative population based community survey. In addition, it addresses various areas such as health care expenditures, adult mortality, birth history, various risk factors, assessment of main chronic health conditions and the coverage of health interventions, in specific additional modules.

The objectives of the survey programme are to: 1. develop a means of providing valid, reliable and comparable information, at low cost, to supplement the information provided by routine health information systems. 2. build the evidence base necessary for policy-makers to monitor if health systems are achieving the desired goals, and to assess if additional investment in health is achieving the desired outcomes. 3. provide policy-makers with the evidence they need to adjust their policies, strategies and programmes as necessary.

Geographic coverage

The survey sampling frame must cover 100% of the country's eligible population, meaning that the entire national territory must be included. This does not mean that every province or territory need be represented in the survey sample but, rather, that all must have a chance (known probability) of being included in the survey sample.

There may be exceptional circumstances that preclude 100% national coverage. Certain areas in certain countries may be impossible to include due to reasons such as accessibility or conflict. All such exceptions must be discussed with WHO sampling experts. If any region must be excluded, it must constitute a coherent area, such as a particular province or region. For example if ¾ of region D in country X is not accessible due to war, the entire region D will be excluded from analysis.

Analysis unit

Households and individuals

Universe

The WHS will include all male and female adults (18 years of age and older) who are not out of the country during the survey period. It should be noted that this includes the population who may be institutionalized for health reasons at the time of the survey: all persons who would have fit the definition of household member at the time of their institutionalisation are included in the eligible population.

If the randomly selected individual is institutionalized short-term (e.g. a 3-day stay at a hospital) the interviewer must return to the household when the individual will have come back to interview him/her. If the randomly selected individual is institutionalized long term (e.g. has been in a nursing home the last 8 years), the interviewer must travel to that institution to interview him/her.

The target population includes any adult, male or female age 18 or over living in private households. Populations in group quarters, on military reservations, or in other non-household living arrangements will not be eligible for the study. People who are in an institution due to a health condition (such as a hospital, hospice, nursing home, home for the aged, etc.) at the time of the visit to the household are interviewed either in the institution or upon their return to their household if this is within a period of two weeks from the first visit to the household.

Kind of data

Sample survey data [ssd]

Sampling procedure

SAMPLING GUIDELINES FOR WHS

Surveys in the WHS program must employ a probability sampling design. This means that every single individual in the sampling frame has a known and non-zero chance of being selected into the survey sample. While a Single Stage Random Sample is ideal if feasible, it is recognized that most sites will carry out Multi-stage Cluster Sampling.

The WHS sampling frame should cover 100% of the eligible population in the surveyed country. This means that every eligible person in the country has a chance of being included in the survey sample. It also means that particular ethnic groups or geographical areas may not be excluded from the sampling frame.

The sample size of the WHS in each country is 5000 persons (exceptions considered on a by-country basis). An adequate number of persons must be drawn from the sampling frame to account for an estimated amount of non-response (refusal to participate, empty houses etc.). The highest estimate of potential non-response and empty households should be used to ensure that the desired sample size is reached at the end of the survey period. This is very important because if, at the end of data collection, the required sample size of 5000 has not been reached additional persons must be selected randomly into the survey sample from the sampling frame. This is both costly and technically complicated (if this situation is to occur, consult WHO sampling experts for assistance), and best avoided by proper planning before data collection begins.

All steps of sampling, including justification for stratification, cluster sizes, probabilities of selection, weights at each stage of selection, and the computer program used for randomization must be communicated to WHO

STRATIFICATION

Stratification is the process by which the population is divided into subgroups. Sampling will then be conducted separately in each subgroup. Strata or subgroups are chosen because evidence is available that they are related to the outcome (e.g. health, responsiveness, mortality, coverage etc.). The strata chosen will vary by country and reflect local conditions. Some examples of factors that can be stratified on are geography (e.g. North, Central, South), level of urbanization (e.g. urban, rural), socio-economic zones, provinces (especially if health administration is primarily under the jurisdiction of provincial authorities), or presence of health facility in area. Strata to be used must be identified by each country and the reasons for selection explicitly justified.

Stratification is strongly recommended at the first stage of sampling. Once the strata have been chosen and justified, all stages of selection will be conducted separately in each stratum. We recommend stratifying on 3-5 factors. It is optimum to have half as many strata (note the difference between stratifying variables, which may be such variables as gender, socio-economic status, province/region etc. and strata, which are the combination of variable categories, for example Male, High socio-economic status, Xingtao Province would be a stratum).

Strata should be as homogenous as possible within and as heterogeneous as possible between. This means that strata should be formulated in such a way that individuals belonging to a stratum should be as similar to each other with respect to key variables as possible and as different as possible from individuals belonging to a different stratum. This maximises the efficiency of stratification in reducing sampling variance.

MULTI-STAGE CLUSTER SELECTION

A cluster is a naturally occurring unit or grouping within the population (e.g. enumeration areas, cities, universities, provinces, hospitals etc.); it is a unit for which the administrative level has clear, nonoverlapping boundaries. Cluster sampling is useful because it avoids having to compile exhaustive lists of every single person in the population. Clusters should be as heterogeneous as possible within and as homogenous as possible between (note that this is the opposite criterion as that for strata). Clusters should be as small as possible (i.e. large administrative units such as Provinces or States are not good clusters) but not so small as to be homogenous.

In cluster sampling, a number of clusters are randomly selected from a list of clusters. Then, either all members of the chosen cluster or a random selection from among them are included in the sample. Multistage sampling is an extension of cluster sampling where a hierarchy of clusters are chosen going from larger to smaller.

In order to carry out multi-stage sampling, one needs to know only the population sizes of the sampling units. For the smallest sampling unit above the elementary unit however, a complete list of all elementary units (households) is needed; in order to be able to randomly select among all households in the TSU, a list of all those households is required. This information may be available from the most recent population census. If the last census was >3 years ago or the information furnished by it was of poor quality or unreliable, the survey staff will have the task of enumerating all households in the smallest randomly selected sampling unit. It is very important to budget for this step if it is necessary and ensure that all households are properly enumerated in order that a representative sample is obtained.

It is always best to have as many clusters in the PSU as possible. The reason for this is that the fewer the number of respondents in each PSU, the lower will be the clustering effect which

Overview

The Associated Press is sharing data from the COVID Impact Survey, which provides statistics about physical health, mental health, economic security and social dynamics related to the coronavirus pandemic in the United States.

Conducted by NORC at the University of Chicago for the Data Foundation, the probability-based survey provides estimates for the United States as a whole, as well as in 10 states (California, Colorado, Florida, Louisiana, Minnesota, Missouri, Montana, New York, Oregon and Texas) and eight metropolitan areas (Atlanta, Baltimore, Birmingham, Chicago, Cleveland, Columbus, Phoenix and Pittsburgh).

The survey is designed to allow for an ongoing gauge of public perception, health and economic status to see what is shifting during the pandemic. When multiple sets of data are available, it will allow for the tracking of how issues ranging from COVID-19 symptoms to economic status change over time.

The survey is focused on three core areas of research:

• Physical Health: Symptoms related to COVID-19, relevant existing conditions and health insurance coverage.
• Economic and Financial Health: Employment, food security, and government cash assistance.
• Social and Mental Health: Communication with friends and family, anxiety and volunteerism. (Questions based on those used on the U.S. Census Bureau’s Current Population Survey.) ## Using this Data - IMPORTANT This is survey data and must be properly weighted during analysis: DO NOT REPORT THIS DATA AS RAW OR AGGREGATE NUMBERS!!

Instead, use our queries linked below or statistical software such as R or SPSS to weight the data.

Queries

If you'd like to create a table to see how people nationally or in your state or city feel about a topic in the survey, use the survey questionnaire and codebook to match a question (the variable label) to a variable name. For instance, "How often have you felt lonely in the past 7 days?" is variable "soc5c".

Nationally: Go to this query and enter soc5c as the variable. Hit the blue Run Query button in the upper right hand corner.

Local or State: To find figures for that response in a specific state, go to this query and type in a state name and soc5c as the variable, and then hit the blue Run Query button in the upper right hand corner.

The resulting sentence you could write out of these queries is: "People in some states are less likely to report loneliness than others. For example, 66% of Louisianans report feeling lonely on none of the last seven days, compared with 52% of Californians. Nationally, 60% of people said they hadn't felt lonely."

Margin of Error

The margin of error for the national and regional surveys is found in the attached methods statement. You will need the margin of error to determine if the comparisons are statistically significant. If the difference is:

• At least twice the margin of error, you can report there is a clear difference.
• At least as large as the margin of error, you can report there is a slight or apparent difference.
• Less than or equal to the margin of error, you can report that the respondents are divided or there is no difference. ## A Note on Timing Survey results will generally be posted under embargo on Tuesday evenings. The data is available for release at 1 p.m. ET Thursdays.

About the Data

The survey data will be provided under embargo in both comma-delimited and statistical formats.

Each set of survey data will be numbered and have the date the embargo lifts in front of it in the format of: 01_April_30_covid_impact_survey. The survey has been organized by the Data Foundation, a non-profit non-partisan think tank, and is sponsored by the Federal Reserve Bank of Minneapolis and the Packard Foundation. It is conducted by NORC at the University of Chicago, a non-partisan research organization. (NORC is not an abbreviation, it part of the organization's formal name.)

Data for the national estimates are collected using the AmeriSpeak Panel, NORC’s probability-based panel designed to be representative of the U.S. household population. Interviews are conducted with adults age 18 and over representing the 50 states and the District of Columbia. Panel members are randomly drawn from AmeriSpeak with a target of achieving 2,000 interviews in each survey. Invited panel members may complete the survey online or by telephone with an NORC telephone interviewer.

Once all the study data have been made final, an iterative raking process is used to adjust for any survey nonresponse as well as any noncoverage or under and oversampling resulting from the study specific sample design. Raking variables include age, gender, census division, race/ethnicity, education, and county groupings based on county level counts of the number of COVID-19 deaths. Demographic weighting variables were obtained from the 2020 Current Population Survey. The count of COVID-19 deaths by county was obtained from USA Facts. The weighted data reflect the U.S. population of adults age 18 and over.

Data for the regional estimates are collected using a multi-mode address-based (ABS) approach that allows residents of each area to complete the interview via web or with an NORC telephone interviewer. All sampled households are mailed a postcard inviting them to complete the survey either online using a unique PIN or via telephone by calling a toll-free number. Interviews are conducted with adults age 18 and over with a target of achieving 400 interviews in each region in each survey.Additional details on the survey methodology and the survey questionnaire are attached below or can be found at https://www.covid-impact.org.

Attribution

Results should be credited to the COVID Impact Survey, conducted by NORC at the University of Chicago for the Data Foundation.

AP Data Distributions

​To learn more about AP's data journalism capabilities for publishers, corporations and financial institutions, go here or email kromano@ap.org.

The New York City Community Health Survey (CHS) is a telephone survey conducted annually by the DOHMH, Division of Epidemiology, Bureau of Epidemiology Services. CHS provides robust data on the health of New Yorkers, including neighborhood, borough, and citywide estimates on a broad range of chronic diseases and behavioral risk factors. The data are analyzed and disseminated to influence health program decisions, and increase the understanding of the relationship between health behavior and health status. For more information see EpiQuery, https://a816-health.nyc.gov/hdi/epiquery/visualizations?PageType=ps&PopulationSource=CHS

The National Survey on Drug Use and Health (NSDUH) provides national and state-level data on the use of tobacco, alcohol, illicit drugs (including non-medical use of prescription drugs) and mental health in the United States. This annual survey involves interviews with approximately 70,000 randomly selected individuals aged 12 and older. NSDUH is sponsored by the Substance Abuse and Mental Health Services Administration (SAMHSA), an agency of the U.S. Public Health Service in the U.S. Department of Health and Human Services (DHHS).

As part of the Detroit Community Health Assessment (CHA) process, the Health Department and community partners worked with the University of Michigan Detroit Metropolitan Area Communities Study (DMACS) team to conduct a representative citywide survey of 1,216 residents to gather relevant information about Detroiters’ experiences, perceptions, priorities and aspirations around community health. The survey was implemented in the summer of 2018 and the results of the survey are included here. The Community Health Assessment report provides a snapshot of health in Detroit using existing data as well as information gathered directly from residents through drawings, photographs, interviews, and a citywide survey.

Graph and download economic data for All Employees, Home Health Care Services (CEU6562160001) from Jan 1985 to May 2025 about health, establishment survey, education, services, employment, and USA.

A national Health Interview Survey (HIS) provides an overall picture of the health status of the population and allows to identify the main health problems, as well as the social and behavioral factors that influence them. This information enables health authorities to pursue a proactive health policy aimed at improving public health and addressing the needs of groups at risk. Researchers, experts and the press use the results of the HIS.

Sciensano organized a large-scale Health Interview Survey (HIS) among the Belgian population for the first time in 1997, and is repeated every 4 to 5 years since. Sciensano will organize the 7th HIS in 2023.

The HIS collects information on a wide range of health topics: physical and mental health, lifestyle, use of health care and preventive services, perception of the physical and social environment, etc. Furthermore, the HIS has been part of the European Health Interview Survey (EHIS) since 2013. This allows not only to study time trends in different health domains and in health inequalities, but also to compare the Belgian results with those of the other EU Member States.

The Washington State Department of Health presents this information as a service to the public. This includes information on the work status, practice characteristics, education, and demographics of healthcare providers, provided in response to the Washington Health Workforce Survey. This is a complete set of data across all of the responding professions. The data dictionary identifies questions that are specific to an individual profession and aren't common to all surveys. The dataset is provided without identifying information for the responding providers. More information on the Washington Health Workforce Survey can be found at www.doh.wa.gov/workforcesurvey This dataset has been federated from https://data.wa.gov/Health/Washington-Health-Workforce-Survey-Data/cvrw-ujje.