Official statistics are produced impartially and free from political influence.
As of 2022, ** percent of people in the United Kingdom thought that the Baby Boomer generation had the best quality of life over their lifetime, compared with just *** percent who thought the pre-war generation had the best quality of life.
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The Cancer Quality of Life Survey is an ongoing national survey run by the NHS in England. The survey is for people in England who have had a cancer diagnosis, with people invited to complete the survey around 18 months after diagnosis. It has been running since September 2020, with a gradual roll-out to all cancer sites. The aim of the survey is to find out how quality of life may have changed for people diagnosed with cancer. The survey asks people who have experienced cancer how they are feeling. Their answers will be compared with information about their cancer diagnosis and treatment. This will help the NHS see where care is working well or not so well, and if any new services are needed. It will help the NHS to improve the way it supports people to live as long and as well as possible. The survey is made up of two questionnaires which measure overall health (EQ-5D) and quality of life (EORTC QLQ-C30). The survey results are reported in an interactive dashboard, including summary score measures and more detailed measures of different aspects of quality of life, including aspects of health (such as mobility), functional categories (such as emotional) and symptoms (such as fatigue). Results are reported by geographies and cancer sites, and with breakdowns by demographic groups. This release includes a new "Data Selection" tab allowing users to toggle between the latest full year of data or all available data. This release also updates the data included in the dashboard, to additionally include data for patients invited from January 2024 to September 2024 and to include response data received up to 11th November 2024. This release provides data for a number of additional broad and detailed cancer types.
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An overview of UK’s progress across ten domains of national well-being. Latest and historical data are provided. Sub-population breakdowns by UK countries and ITL1 regions, age and sex, as well as quality information, are included where available.
Carried out every four years, the European Quality of Life Survey (EQLS) examines both the objective circumstances of European citizens' lives and how they feel about those circumstances and their lives in general. It collects data on a range of issues, such as employment, income, education, housing, family, health and work-life balance. It also looks at subjective topics, such as people's levels of happiness, life satisfaction, and perceived quality of society. By running the survey regularly, it has also become possible to track key trends in the quality of people's lives over time. Previous surveys have shown, for instance, that people are having greater difficulty making ends meet since the economic crisis began. In many countries, they also feel that there is now more tension between people from different ethnic groups. And across Europe, people now trust their governments less than they did before. However, people still continue to get the greatest satisfaction from their family life and personal relationships.
Over the years, the EQLS has developed into a valuable set of indicators which complements traditional indicators of economic growth and living standard such as GDP or income. The EQLS indicators are more inclusive of environmental and social aspects of progress and therefore are easily integrated into the decision-making process and taken up by public debate at EU and national levels in the European Union.
In each wave a sample of adult population has been selected randomly for a face to face interview. In view of the prospective European enlargements the geographical coverage of the survey has expanded over time from 28 countries in 2003 to 34 countries in 2011-12.
Further information about the survey can be found on the European Foundation for the Improvement of Living and Working Conditions (Eurofound) EQLS web pages.
For the second edition (January 2014) the data file has been updated with a new total weighting variable. See documentation for further details and see also the updated version of the EQLS integrated file, held under SN 7348).
This statistic displays the level of self-care of adults in England, by gender, according to the EQ-5D dimension test in 2012. In this year, 96 percent of men and 95 percent of women had no problems with self-care.
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This study is the fifth in a series of national surveys commissioned by the Department of the Environment to investigate people's environmental concerns, awareness and behaviour. The previous four surveys were carried out in 1986, 1989, 1993 and 1996-1997. Users should note that the UK Data Archive currently holds the first three surveys in addition to this one (SNs 2684, 2685 and 3329), but not the fourth (conducted in 1996-1997).
The objectives of the research were to:
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Confidence intervals and sample sizes for quarterly estimates of personal well-being in the UK.
As of June 2025, the average score for how happy people felt in the UK was 7.1 out of ten, people aged 70 and over reporting an average score of 7.7, the highest among the provided demographics.
Live sporting events have the ability to bring likeminded people together in support of their favorite sports teams. During an August 2020 survey in the United Kingdom, around 36 percent of sports fans stated that watching or attending live sporting events was important to their overall quality of life.
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This indicator measures the health-related quality of life for people who identify themselves as having three or more long-term conditions. This indicator measures how successfully the NHS is supporting people with multiple long-term conditions to live as normal a life as possible. This indicator helps people understand whether health-related quality of life is improving over time for the population with multiple long-term conditions. There are no planned future updates for this indicator. The methodology for the indicator requires review, this is not actively being progressed at this time. Legacy unique identifier: P01756
This statistic shows the results of a survey on the quality of care across all end of life services in England in 2015. Over 70 percent of respondents said the quality of services provided was good, with 12.1 percent saying it was outstanding.
This research project was carried out to develop a dataset to produce normative values for healthy children using the Generic Children's Quality of Life (GCQ) measure and to assess the reliability and validity of the measure. The study aimed to assess the quality of life of a population sample of schoolchildren.
The GCQ measure has been developed to allow comparison between chronically ill children and the general child population. The measure assesses how the child views his or her life, and how they would like their life to be. Quality of life is measured as the discrepancy between the two viewpoints. This large community-based survey aimed to establish GCQ norm values for children aged 6-14 years. The respondents to the survey were pupils at a sample of schools stratified by geographical location and social need into four categories: rural affluent; rural low affluence; urban affluent and urban low affluence.
For the second edition of the study (September 2007), some new information was added to the user guide.
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CPRD GOLD linked Quality of Life of Colorectal Cancer Survivors in England: Patient Reported Outcome Measures (PROMs) survey, is a national survey that was commissioned by the Department of Health as a follow-on from the pilot study in July 2011 undertaken to confirm the value of collecting PROMs data on breast, prostate, colorectal and non-Hodgkin’s lymphoma. It includes survey data from 34,467 patients aged 16 years and over with an incident colorectal cancer diagnosis during Jan 2010 Dec 2011. Outcome items in the survey are made up of Euroqol 5-level (EQ-5D), Functional Assessment of Cancer Therapy (FACT), and Social Difficulties Inventory (SDI) items.
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CPRD Aurum linked Quality of Life of Cancer Survivors in England: Pilot Survey (2011) was commissioned by the Department of Health as part of the National Cancer Survivorship Initiative (NCSI). The survey was conducted by Quality Health in conjunction with three cancer registries in England. The survey measured the overall quality of life of representative samples of cancer survivors with breast, colorectal cancer, prostate cancer and non-Hodgkin’s lymphoma (NHL) diagnosed during July 2006 - July 2010. Quality of life was assessed at four different time points after diagnosis at approximately one, two, three or five years. As this was a pilot survey, numbers are small and data governance issues will need to be carefully considered on a study by study basis. Outcome items in the survey are made up of Euroqol 5-level (EQ-5D), Functional Assessment of Cancer Therapy (FACT), and Social Difficulties Inventory (SDI) items.
Wellbeing in Developing Countries is a series of studies which aim to develop a conceptual and methodological approach to understanding the social and cultural construction of wellbeing in developing countries. The Wellbeing in Developing Countries Research Group (WeD), based at the University of Bath, drew on knowledge and expertise from three different departments (Economics and International Development, Social and Policy Sciences and Psychology) as well as a network of overseas contacts. The international, interdisciplinary team formed a major programme of comparative research, focused on six communities in each of four countries: Ethiopia, Thailand, Peru and Bangladesh. All sites within the countries have been given anonymous site names, with the exception of Ethiopia where the team chose to follow an alternative locally agreed procedure on anonymisation. Data can be matched across studies using the HOUSEKEY (Site code and household number).
The research raises fundamental questions both for the academic study of development, and for the policy community. The WeD arrived at the following definition of wellbeing through their research: "Wellbeing is a state of being with others, where human needs are met, where one can act meaningfully to pursue one's goals, and where one enjoys a satisfactory quality of life".
Further information about the project can be found on the WeD website and the ESRC Award webpage.
Wellbeing in Developing Countries: Quality of Life, 2004-2005 comprises the Quality of Life (QoL) Survey which was carried out in each of the four countries. The QoL was administered to approx 370 men and women in each country (approximately 60 per research site) in the local language by a team of interviewers selected by each of the country teams. The majority of respondents also completed the other surveys that form part of this research project and are available from the UKDA under GN 33394. The remainder were sampled proportionately according to age, socio-economic status, ethnicity and religion. For each country there is one data file at the individual level.
This is a point feature service which shows the following "Life expectancy at birth. Population weighting applying MSOA Life expectancy to GP registered patients." This description was taken from Public Health England's metadata on the GP profiles. This data was downloaded Febuary 2015. Esri UK accepts no responbibility over the quality of the data or ownership. All content is available under the Open Government Licence, except where otherwise stated
This is a point feature service which shows the following "Life expectancy at birth. Population weighting applying MSOA Life expectancy to GP registered patients." This description was taken from Public Health England's metadata on the GP profiles. This data was downloaded Febuary 2015. Esri UK accepts no responbibility over the quality of the data or ownership. All content is available under the Open Government Licence, except where otherwise stated
CC0 1.0 Universal Public Domain Dedicationhttps://creativecommons.org/publicdomain/zero/1.0/
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The Independent Steering Group for the study gave permission for the research team to share the WHOQOL-BREF data.Imputed data are included here, based on the method used inMcConachie, H., Mason, D., Parr, J. R., Garland, D., Wilson, C., & Rodgers, J. (2018). Enhancing the validity of a quality of life measure for autistic people. Journal of autism and developmental disorders, 48(5), 1596-1611.
Official statistics are produced impartially and free from political influence.