Literature DB >> 17059488

The effect of involvement in participatory research on parent researchers in a Sure Start programme.

Ann Rowe1.   

Abstract

Involving service users, patients and members of local communities in health and social care research is becoming increasingly common. However, surprisingly little research has been carried out to examine the experiences of such lay researchers. This paper presents the findings of a study to investigate the experiences of a group of parent researchers involved in a community survey within a UK Sure Start programme. The survey was undertaken to provide insight into the early impact of the programme and inform Sure Start programme expansion. Researchers were recruited from the local community and were given an accredited training programme, before working on the development of the research itself. They took a lead role in the development, data collection, analysis and report writing phases of the survey and have been actively involved with the dissemination of findings. In order to gain insight into the experiences of the lay researchers involved in this work, three separate methods were used to collect data: questionnaires before and after the study, a focus group at the end of the data collection phase and by analysis of personal diaries kept by the parent researchers. Findings reported include lay researchers responses to the accredited training programme, the development of new skills and understanding, access and the conduct of interviews and the impact of the work both for Sure Start and the researchers themselves. Some of the strengths and difficulties of participatory research are discussed and comment made on the extent to which lay involvement impacted on the conduct of the survey.

Entities:  

Mesh:

Year:  2006        PMID: 17059488     DOI: 10.1111/j.1365-2524.2006.00632.x

Source DB:  PubMed          Journal:  Health Soc Care Community        ISSN: 0966-0410


  12 in total

1.  What is involvement in research and what does it achieve? Reflections on a pilot study of the personal costs of stroke.

Authors:  Christopher McKevitt; Nina Fudge; Charles Wolfe
Journal:  Health Expect       Date:  2009-08-19       Impact factor: 3.377

2.  Patient and public involvement in patient-reported outcome measures: evolution not revolution.

Authors:  Sophie Staniszewska; Kirstie L Haywood; Jo Brett; Liz Tutton
Journal:  Patient       Date:  2012       Impact factor: 3.883

Review 3.  Mapping the impact of patient and public involvement on health and social care research: a systematic review.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Health Expect       Date:  2012-07-19       Impact factor: 3.377

4.  Experiential Learning Through Participatory Action Research in Public Health Supports Community-Based Training of Future Health Professionals.

Authors:  Lisa K Marriott; Adam C Lipus; Laurie Choate; Jamie Smith; Leigh Coppola; William E Cameron; Jackilen Shannon
Journal:  Pedagogy Health Promot       Date:  2015-08-27

5.  House Chats as a Grassroots Engagement Methodology in Community-Based Participatory Research: The WE Project, Petersburg.

Authors:  Maghboeba Mosavel; Dwala Ferrell; Jessica Gokee LaRose
Journal:  Prog Community Health Partnersh       Date:  2016

6.  Co-development and Usability Testing of Research 101: A Patient-Oriented Research Curriculum in Child Health (PORCCH) E-Learning Module for Patients and Families.

Authors:  Catharine M Walsh; Nicola L Jones; Graham A McCreath; Veronik Connan; Linda Pires; Autumn Q H Chen; Aliza Karoly; Colin Macarthur
Journal:  Front Pediatr       Date:  2022-07-06       Impact factor: 3.569

Review 7.  A systematic review of the impact of patient and public involvement on service users, researchers and communities.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Patient       Date:  2014       Impact factor: 3.883

8.  Researching health inequalities with Community Researchers: practical, methodological and ethical challenges of an 'inclusive' research approach.

Authors:  Sarah Salway; Punita Chowbey; Elizabeth Such; Beverly Ferguson
Journal:  Res Involv Engagem       Date:  2015-08-13

9.  'I'm sure we made it a better study…': Experiences of adults with intellectual disabilities and parent carers of patient and public involvement in a health research study.

Authors:  Carole Beighton; Christina Victor; Iain M Carey; Fay Hosking; Steve DeWilde; Derek G Cook; Paula Manners; Tess Harris
Journal:  J Intellect Disabil       Date:  2017-08-16

Review 10.  How and why should we engage parents as co-researchers in health research? A scoping review of current practices.

Authors:  Shuoqi Shen; Krissy A R Doyle-Thomas; Lori Beesley; Amir Karmali; Laura Williams; Nadia Tanel; Amy C McPherson
Journal:  Health Expect       Date:  2016-08-12       Impact factor: 3.377

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.