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Wellbeing of Family Carers of Adults With Intellectual Disabilities During the COVID‐19 Pandemic in the UK: Longitudinal Study

  • Paul A. Thompson
  • , Eleanor Summers
  • , Sue Caton
  • , Nikita Hayden
  • , Stuart Todd
  • , Edward Oloidi
  • , Laurence Taggart
  • , Rosemary Kelly
  • , Jill Bradshaw
  • , Roseann Maguire
  • , Andrew Jahoda
  • , Chris Hatton
  • , Richard P. Hastings

Research output: Contribution to journalArticlepeer-review

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Abstract

Background: Longitudinal studies of family carers of people with intellectual disabilities during the COVID-19 pandemic have been very rare. This study investigated trajectories of family-carer wellbeing and the impact of the caring role on carers' health over four time points measured during the COVID-19 pandemic and after all public health restrictions had been lifted (between December 2020 and late 2022) across the United Kingdom. Methods: Family carers of adults with intellectual disabilities participated through a co-designed, online survey at four time points across the pandemic (2020–2022). Growth models were used to determine the change in family-carer wellbeing (n = 312) and the impact of the caring role on carers' health across the pandemic and what factors were associated with these outcomes. We explored associations between profound and multiple intellectual disabilities (PMID), the cared-for person's individual wellbeing, the cared-for person's age, whether the cared-for person lived with their family and family-carer wellbeing and impact of caring trajectories. Results: Overall, family-carer wellbeing improved, and the impact of the caring role on carers' health reduced across the time period. If the cared-for person had PMID was associated with greater degrees of depression and stress for caregivers and thus increased the impact of the caring role on carers' health, but it was not associated with carer wellbeing. Similarly, the reduction in individual wellbeing of the cared-for person and the caregiver's perception of this person's wellbeing was also significantly associated with increased impact of the caring role on carers' health and carer wellbeing. There was no evidence that age of cared-for person was predictive of either outcome, and there were mixed findings on whether living at home was an associated factor for either outcome. Conclusions: Overall, family-carer wellbeing improved, and the impact of the caring role on carers' health reduced across the time period, but the cared-for persons' poorer wellbeing and complex needs (indexed by the presence of PMID) were associated with negative impacts on family carers during the pandemic period.

Original languageEnglish
Pages (from-to)265-273
Number of pages9
JournalJournal of Intellectual Disability Research
Volume69
Issue number4
Early online date24 Dec 2024
DOIs
Publication statusPublished (in print/issue) - 20 Apr 2025

Bibliographical note

Publisher Copyright:
© 2024 The Author(s). Journal of Intellectual Disability Research published by John Wiley & Sons and MENCAP.

Data Availability Statement

A quantitative dataset will be archived online in a form that will be available to researchers after all waves of data collection for the project have been completed.

Funding

Research reported in this paper was funded by the UK Research and Innovation (Medical Research Council) and supported by the Department for Health and Social Care (National Institute for Health Research) as part of the UKRI\u2010DHSC COVID\u201019 Rapid Response Rolling Call (grant number COV0196) and also the National Institute for Health Research Policy Research Programme (grant number NIHR204404). The views expressed in this publication are those of the authors and not necessarily those of DHSC, NIHR, UKRI or MRC. Funding: We would like to thank the following collaborating organisations and participants who contributed to this research: All Wales People First, Learning Disability Wales, All Wales Forum of Parents and Carers of People with Learning Disabilities, Scottish Commission for Learning Disability, Promoting a More Inclusive Society (PAMIS), Positive Futures, Mencap Northern Ireland, Learning Disability England, PMLD Link, Positive Futures, CAN Northern Ireland, Families Involved in Northern Ireland (FINI).

FundersFunder number
Positive Futures
Medical Research CouncilMR/V028596/1
COV0196
NIHR204404

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Covid-19
    • family-carer wellbeing
    • impact of caring
    • intellectual disability
    • COVID-19
    • Humans
    • Middle Aged
    • Family/psychology
    • Male
    • United Kingdom
    • Caregivers/psychology
    • Intellectual Disability/nursing
    • COVID-19/psychology
    • Young Adult
    • Adult
    • Female
    • Aged
    • Longitudinal Studies

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