3 datasets found
  1. d

    [MI] National Data Opt-Out

    • digital.nhs.uk
    Updated Aug 12, 2021
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    (2021). [MI] National Data Opt-Out [Dataset]. https://digital.nhs.uk/data-and-information/publications/statistical/national-data-opt-out
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    Dataset updated
    Aug 12, 2021
    License

    https://digital.nhs.uk/about-nhs-digital/terms-and-conditionshttps://digital.nhs.uk/about-nhs-digital/terms-and-conditions

    Time period covered
    Sep 1, 2020 - Aug 1, 2021
    Description

    This publication provides statistics on the number of unique NHS numbers with an associated national data opt-out. The national data opt-out was introduced on 25 May 2018. It was introduced following recommendations from the National Data Guardian. It indicates that a patient does not want their confidential patient information to be shared for purposes beyond their individual care across the health and care system in England. The service allows individuals to set a national data opt-out or reverse a previously set opt-out. It replaced the previous type 2 opt-outs which patients registered via their GP Practice. Previous type 2 opt-outs have been converted to national data opt-outs each month, until November 2018. This is why the monthly increase in opt-outs decreases from December 2018 onward. This publication includes the number of people who have a national data opt-out, broken down by age, gender and a variety of geographical breakdowns. From June 2020 the methodology for reporting NDOP changed, representing a break in time series. Therefore, caution should be used when comparing data to publications prior to June 2020. The number of deceased people with an active NDOP has been captured and reported for the first time in June 2020. Please note that this publication is no longer released monthly. It is released annually or when the national opt-out rate changes by more than 0.1 per cent. Prior to September 2020 there is a slight inflation of less than 0.05 percent in the number of National Data Opt-outs. This is due to an issue with the data processing, which has been resolved and does not affect data after September 2020. This issue does not disproportionately affect any single breakdown, including geographies. Please take this into consideration when using the data. Management information describes aggregate information collated and used in the normal course of business to inform operational delivery, policy development or the management of organisational performance. It is usually based on administrative data but can also be a product of survey data. We publish these management information to ensure equality of access and provide wider public value. Please note, there are instances of legacy CCG codes in the Resident Geography CSV file due to outdated reference tables which will be corrected in future publications.

  2. Evidence for Equality National Survey: a Survey of Ethnic Minorities During...

    • beta.ukdataservice.ac.uk
    Updated 2024
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    N. Finney; J. Nazroo; N. Shlomo; D. Kapadia; L. Becares; B. Byrne (2024). Evidence for Equality National Survey: a Survey of Ethnic Minorities During the COVID-19 Pandemic, 2021 [Dataset]. http://doi.org/10.5255/ukda-sn-9116-1
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    Dataset updated
    2024
    Dataset provided by
    UK Data Servicehttps://ukdataservice.ac.uk/
    datacite
    Authors
    N. Finney; J. Nazroo; N. Shlomo; D. Kapadia; L. Becares; B. Byrne
    Description
    The Centre on the Dynamics of Ethnicity (CoDE), led by the University of Manchester with the Universities of St Andrews, Sussex, Glasgow, Edinburgh, LSE, Goldsmiths, King's College London and Manchester Metropolitan University, designed and carried out the Evidence for Equality National Survey (EVENS), with Ipsos as the survey partner. EVENS documents the lives of ethnic and religious minorities in Britain during the coronavirus pandemic and is, to date, the largest and most comprehensive survey to do so.

    EVENS used online and telephone survey modes, multiple languages, and a suite of recruitment strategies to reach the target audience. Words of Colour coordinated the recruitment strategies to direct participants to the survey, and partnerships with 13 voluntary, community and social enterprise (VCSE) organisations[1] helped to recruit participants for the survey.

    The ambition of EVENS was to better represent ethnic and religious minorities compared to existing data sources regarding the range and diversity of represented minority population groups and the topic coverage. Thus, the EVENS survey used an 'open' survey approach, which requires participants to opt-in to the survey instead of probability-based approaches that invite individuals to participate following their identification within a pre-defined sampling frame. This 'open' approach sought to overcome some of the limitations of probability-based methods in order to reach a large number and diverse mix of people from religious and ethnic minorities.

    EVENS included a wide range of research and policy questions, including education, employment and economic well-being, housing, social, cultural and political participation, health, and experiences of racism and discrimination, particularly with respect to the impact of the COVID-19 pandemic. Crucially, EVENS covered a full range of racial, ethnic and religious groups, including those often unrepresented in such work (such as Chinese, Jewish and Traveller groups), resulting in the participation of 14,215 participants, including 9,702 ethnic minority participants and a general population sample of 4,513, composed of White people who classified themselves as English, Welsh, Scottish, Northern Irish, and British. Data collection covered the period between 16 February 2021 and 14 August 2021.

    Further information about the study can be found on the EVENS project website.

    A teaching dataset based on the main EVENS study is available from the UKDS under SN 9249.

    [1] The VCSE organisations included Business in the Community, BEMIS (Scotland), Ethnic Minorities and Youth Support Team (Wales), Friends, Families and Travellers, Institute for Jewish Policy Research, Migrants' Rights Networks, Muslim Council Britain, NHS Race and Health Observatory, Operation Black Vote, Race Equality Foundation, Runnymede Trust, Stuart Hall Foundation, and The Ubele Initiative.
  3. n

    FOI-01400

    • opendata.nhsbsa.net
    Updated Sep 28, 2023
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    (2023). FOI-01400 [Dataset]. https://opendata.nhsbsa.net/dataset/foi-01400
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    Dataset updated
    Sep 28, 2023
    Description

    In order to help me not to misrepresent the data, I would like you to provide further details under the Freedom of Information Act. Please provide: a) Divided by total pensionable pay by salary bands, and by the financial years 2018/19, 2019/20, 2020/21, 2021/22, and 2022/23, the number of members who have returned into the scheme, having opted out, in the same financial year b) Divided by total pensionable pay and by salary bands, and by the financial years 2018/19, 2019/20, 2020/21, 2021/22, and 2022/23, the total number of all members in the scheme at the start of the year before considering considering any opt-outs I would also like to clarify for certainty, when you say "Members have been counted once for each financial year (01/04 – 31/03) in which they opted out", does this mean if a member opted out of the scheme in 2018, they would be counted in every year since? Must that member decide at the start of each financial year that they are opting out? I understand it is not a reflection of the members' annual salary. Please provide them in these categories: Under £20,000, £20,000 - £29,999, £30,000 - £39,999, £40,000 - £49,999, £50,000 - £59,999, £60,000 - £69,999, £70,000 - £79,999, £80,000 - £89,999, £90,000 - £99,999 £100,000 and Over On the second point, I am trying to understand the number of members eligible for the scheme at the start of each financial year. If this is not possible, just the number of active members in the scheme in total at the start of each financial year please. Response A copy of the information is attached. Please read the below notes to ensure correct understanding of the data. The scheme year is 1 April to 31 March. Although financial years are mentioned, records are held in Scheme year and have been provided based on 1 April. For part a, the total TPP bracket is not a reflection of the members annual salary. The volumes are of the members that have opted out and returned to the service again during the same scheme year. In case a member opts out multiple times and returns to a post during the same year, it is still considered only once for the count (unless they return in the next year). Part b relates to members who were active at the start of the Scheme year (1st April). This does not represent the members eligible to join (or opt-out) of the scheme. We have no visibility of those members who opt-out of auto-enrolment and have no idea if members who opted out previously are still opted out (and therefore eligible to opt-in and be considered in any calculated 'opt out rate') or have since left NHS employment completely.

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(2021). [MI] National Data Opt-Out [Dataset]. https://digital.nhs.uk/data-and-information/publications/statistical/national-data-opt-out

[MI] National Data Opt-Out

[MI] National Data Opt-out, August 2021

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16 scholarly articles cite this dataset (View in Google Scholar)
Dataset updated
Aug 12, 2021
License

https://digital.nhs.uk/about-nhs-digital/terms-and-conditionshttps://digital.nhs.uk/about-nhs-digital/terms-and-conditions

Time period covered
Sep 1, 2020 - Aug 1, 2021
Description

This publication provides statistics on the number of unique NHS numbers with an associated national data opt-out. The national data opt-out was introduced on 25 May 2018. It was introduced following recommendations from the National Data Guardian. It indicates that a patient does not want their confidential patient information to be shared for purposes beyond their individual care across the health and care system in England. The service allows individuals to set a national data opt-out or reverse a previously set opt-out. It replaced the previous type 2 opt-outs which patients registered via their GP Practice. Previous type 2 opt-outs have been converted to national data opt-outs each month, until November 2018. This is why the monthly increase in opt-outs decreases from December 2018 onward. This publication includes the number of people who have a national data opt-out, broken down by age, gender and a variety of geographical breakdowns. From June 2020 the methodology for reporting NDOP changed, representing a break in time series. Therefore, caution should be used when comparing data to publications prior to June 2020. The number of deceased people with an active NDOP has been captured and reported for the first time in June 2020. Please note that this publication is no longer released monthly. It is released annually or when the national opt-out rate changes by more than 0.1 per cent. Prior to September 2020 there is a slight inflation of less than 0.05 percent in the number of National Data Opt-outs. This is due to an issue with the data processing, which has been resolved and does not affect data after September 2020. This issue does not disproportionately affect any single breakdown, including geographies. Please take this into consideration when using the data. Management information describes aggregate information collated and used in the normal course of business to inform operational delivery, policy development or the management of organisational performance. It is usually based on administrative data but can also be a product of survey data. We publish these management information to ensure equality of access and provide wider public value. Please note, there are instances of legacy CCG codes in the Resident Geography CSV file due to outdated reference tables which will be corrected in future publications.

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