Enabling participation of Black and Minority Ethnic (BME) and seldom-heard communities in health research: A case study from the SCAMP adolescent cohort study
Our inquiry investigated the barriers to, and facilitators for, the involvement of Black and Minority Ethnic (BME) and ‘seldom-heard’ communities, in a study researching the impact of mobile phone and wireless device usage on adolescents’ cognition, behaviour and mental health. The aim was to co-pro...
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doaj-45a6074c91ae4d27a7b98fcff28406062020-12-16T09:42:41ZengUCL PressResearch for All2399-81212020-08-0110.14324/RFA.04.2.06Enabling participation of Black and Minority Ethnic (BME) and seldom-heard communities in health research: A case study from the SCAMP adolescent cohort studyJane BrutonKathryn JonesRosemary H JenkinsBethan DaviesHelen WardMireille ToledanoOur inquiry investigated the barriers to, and facilitators for, the involvement of Black and Minority Ethnic (BME) and ‘seldom-heard’ communities, in a study researching the impact of mobile phone and wireless device usage on adolescents’ cognition, behaviour and mental health. The aim was to co-produce solutions to increase participation, and we used focus groups, telephone interviews, a community event and a public and patient involvement (PPI) café to conduct the inquiry. Five themes emerged from the data: two enablers – the value and benefits of research; and three barriers – concerns about research and about communication, and practical constraints. A central cross-cutting theme, the concept of trust, was evident from the data, and extended across all themes, including across the solutions to non-participation. When the data collection and analysis were completed, we ran a symposium for researchers and members of the public to share our findings and to co-produce solutions. The symposium generated ideas about improving participation, including tailoring participant information, engaging with local advocates and involving people in research design and delivery.https://ucl.scienceopen.com/hosted-document?doi=10.14324/RFA.04.2.06 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jane Bruton Kathryn Jones Rosemary H Jenkins Bethan Davies Helen Ward Mireille Toledano |
spellingShingle |
Jane Bruton Kathryn Jones Rosemary H Jenkins Bethan Davies Helen Ward Mireille Toledano Enabling participation of Black and Minority Ethnic (BME) and seldom-heard communities in health research: A case study from the SCAMP adolescent cohort study Research for All |
author_facet |
Jane Bruton Kathryn Jones Rosemary H Jenkins Bethan Davies Helen Ward Mireille Toledano |
author_sort |
Jane Bruton |
title |
Enabling participation of Black and Minority Ethnic (BME) and seldom-heard communities in health research: A case study from the SCAMP adolescent cohort study |
title_short |
Enabling participation of Black and Minority Ethnic (BME) and seldom-heard communities in health research: A case study from the SCAMP adolescent cohort study |
title_full |
Enabling participation of Black and Minority Ethnic (BME) and seldom-heard communities in health research: A case study from the SCAMP adolescent cohort study |
title_fullStr |
Enabling participation of Black and Minority Ethnic (BME) and seldom-heard communities in health research: A case study from the SCAMP adolescent cohort study |
title_full_unstemmed |
Enabling participation of Black and Minority Ethnic (BME) and seldom-heard communities in health research: A case study from the SCAMP adolescent cohort study |
title_sort |
enabling participation of black and minority ethnic (bme) and seldom-heard communities in health research: a case study from the scamp adolescent cohort study |
publisher |
UCL Press |
series |
Research for All |
issn |
2399-8121 |
publishDate |
2020-08-01 |
description |
Our inquiry investigated the barriers to, and facilitators for, the involvement of Black and Minority Ethnic (BME) and ‘seldom-heard’ communities, in a study researching the impact of mobile phone and wireless device usage on adolescents’ cognition, behaviour and mental health. The aim was to co-produce solutions to increase participation, and we used focus groups, telephone interviews, a community event and a public and patient involvement (PPI) café to conduct the inquiry. Five themes emerged from the data: two enablers – the value and benefits of research; and three barriers – concerns about research and about communication, and practical constraints. A central cross-cutting theme, the concept of trust, was evident from the data, and extended across all themes, including across the solutions to non-participation. When the data collection and analysis were completed, we ran a symposium for researchers and members of the public to share our findings and to co-produce solutions. The symposium generated ideas about improving participation, including tailoring participant information, engaging with local advocates and involving people in research design and delivery. |
url |
https://ucl.scienceopen.com/hosted-document?doi=10.14324/RFA.04.2.06 |
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