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One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial
INTRODUCTION: People with intellectual disability (ID) are more likely to experience loneliness and have smaller social networks, which increases vulnerability to depression. Befriending may reduce depressive symptoms in other populations, but randomised controlled trials (RCTs) have not been carrie...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7311030/ https://www.ncbi.nlm.nih.gov/pubmed/32565450 http://dx.doi.org/10.1136/bmjopen-2019-033989 |
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author | Ali, Afia Mckenzie, Emma Hassiotis, Angela Priebe, Stefan Lloyd-Evans, Brynmor Omar, Rumana Jones, Rebecca Panca, Monica Fernandez, Vincent Finning, Sally Moore, Shirley O'Connor, Danielle Roe, Christine King, Michael |
author_facet | Ali, Afia Mckenzie, Emma Hassiotis, Angela Priebe, Stefan Lloyd-Evans, Brynmor Omar, Rumana Jones, Rebecca Panca, Monica Fernandez, Vincent Finning, Sally Moore, Shirley O'Connor, Danielle Roe, Christine King, Michael |
author_sort | Ali, Afia |
collection | PubMed |
description | INTRODUCTION: People with intellectual disability (ID) are more likely to experience loneliness and have smaller social networks, which increases vulnerability to depression. Befriending may reduce depressive symptoms in other populations, but randomised controlled trials (RCTs) have not been carried out in this population. This pilot study aims to assess the acceptability and feasibility of carrying out a full RCT of one-to-one befriending by volunteers for people with ID, compared with an active control group. METHODS AND ANALYSIS: The trial aims to recruit 40 participants with ID. Participants in the intervention arm will receive weekly visits from a volunteer over 6 months. Community befriending schemes will recruit, train, supervise volunteers and match them to individuals with ID. Both groups will receive a booklet about local activities and have access to usual care. Health and social outcomes will be measured at the end of the intervention and 6 months’ follow-up. The following outcomes will be assessed: (1) recruitment and retention of individuals with ID and volunteers in the trial, (2) adverse events related to the intervention, (3) the acceptability of the intervention, (4) whether the intervention is delivered as intended, (5) changes in health and social outcomes and (6) the feasibility of carrying out a cost-effectiveness analysis in a full trial. Qualitative data from participants, volunteers, staff and carers will identify barriers and facilitators of a future full trial. ETHICS AND DISSEMINATION: The study has been approved by the London City and East Research Ethics Committee (reference 18/LO/2188). The findings will be presented at conferences and published in a peer-reviewed journal and in the National Institute of Health Research journals library. A public engagement seminar will be held at the end of the study aimed at key stakeholders. TRIAL REGISTRATION NUMBER: ISRCTN63779614. |
format | Online Article Text |
id | pubmed-7311030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-73110302020-06-26 One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial Ali, Afia Mckenzie, Emma Hassiotis, Angela Priebe, Stefan Lloyd-Evans, Brynmor Omar, Rumana Jones, Rebecca Panca, Monica Fernandez, Vincent Finning, Sally Moore, Shirley O'Connor, Danielle Roe, Christine King, Michael BMJ Open Mental Health INTRODUCTION: People with intellectual disability (ID) are more likely to experience loneliness and have smaller social networks, which increases vulnerability to depression. Befriending may reduce depressive symptoms in other populations, but randomised controlled trials (RCTs) have not been carried out in this population. This pilot study aims to assess the acceptability and feasibility of carrying out a full RCT of one-to-one befriending by volunteers for people with ID, compared with an active control group. METHODS AND ANALYSIS: The trial aims to recruit 40 participants with ID. Participants in the intervention arm will receive weekly visits from a volunteer over 6 months. Community befriending schemes will recruit, train, supervise volunteers and match them to individuals with ID. Both groups will receive a booklet about local activities and have access to usual care. Health and social outcomes will be measured at the end of the intervention and 6 months’ follow-up. The following outcomes will be assessed: (1) recruitment and retention of individuals with ID and volunteers in the trial, (2) adverse events related to the intervention, (3) the acceptability of the intervention, (4) whether the intervention is delivered as intended, (5) changes in health and social outcomes and (6) the feasibility of carrying out a cost-effectiveness analysis in a full trial. Qualitative data from participants, volunteers, staff and carers will identify barriers and facilitators of a future full trial. ETHICS AND DISSEMINATION: The study has been approved by the London City and East Research Ethics Committee (reference 18/LO/2188). The findings will be presented at conferences and published in a peer-reviewed journal and in the National Institute of Health Research journals library. A public engagement seminar will be held at the end of the study aimed at key stakeholders. TRIAL REGISTRATION NUMBER: ISRCTN63779614. BMJ Publishing Group 2020-06-21 /pmc/articles/PMC7311030/ /pubmed/32565450 http://dx.doi.org/10.1136/bmjopen-2019-033989 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Mental Health Ali, Afia Mckenzie, Emma Hassiotis, Angela Priebe, Stefan Lloyd-Evans, Brynmor Omar, Rumana Jones, Rebecca Panca, Monica Fernandez, Vincent Finning, Sally Moore, Shirley O'Connor, Danielle Roe, Christine King, Michael One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial |
title | One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial |
title_full | One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial |
title_fullStr | One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial |
title_full_unstemmed | One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial |
title_short | One-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial |
title_sort | one-to-one befriending for people with intellectual disability and symptoms of depression: protocol for a pilot randomised controlled trial |
topic | Mental Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7311030/ https://www.ncbi.nlm.nih.gov/pubmed/32565450 http://dx.doi.org/10.1136/bmjopen-2019-033989 |
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