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Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?

BACKGROUND: Contradictory evidence exists about the emotional burden of participating in qualitative research for palliative care patients and carers and this raises questions about whether this type of research is ethically justified in a vulnerable population. This study aimed to investigate palli...

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Autores principales: Gysels, Marjolein, Shipman, Cathy, Higginson, Irene J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2383914/
https://www.ncbi.nlm.nih.gov/pubmed/18435846
http://dx.doi.org/10.1186/1472-6939-9-7
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author Gysels, Marjolein
Shipman, Cathy
Higginson, Irene J
author_facet Gysels, Marjolein
Shipman, Cathy
Higginson, Irene J
author_sort Gysels, Marjolein
collection PubMed
description BACKGROUND: Contradictory evidence exists about the emotional burden of participating in qualitative research for palliative care patients and carers and this raises questions about whether this type of research is ethically justified in a vulnerable population. This study aimed to investigate palliative care patients' and carers' perceptions of the benefits and problems associated with open interviews and to understand what causes distress and what is helpful about participation in a research interview. METHODS: A descriptive qualitative study. The data were collected in the context of two studies exploring the experiences of care of palliative care patients and carers. The interviews ended with questions about patients' and carers' thoughts on participating in the studies and whether this had been a distressing or helpful event. We used a qualitative descriptive analysis strategy generated from the interviews and the observational and interactional data obtained in the course of the study. RESULTS: The interviews were considered helpful: sharing problems was therapeutic and being able to contribute to research was empowering. However, thinking about the future was reported to be the most challenging. Consent forms were sometimes read with apprehension and being physically unable to sign was experienced as upsetting. Interviewing patients and carers separately was sometimes difficult and not always possible. CONCLUSION: The open interview enables the perspectives of patients and carers to be heard, unfettered from the structure of closed questions. It also enables those patients or carers to take part who would be unable to participate in other study designs. The context is at least as important as the format of the research interview taking into account the relational circumstances with carers and appropriate ways of obtaining informed consent. Retrospective consent could be a solution to enhancing participants control over the interview.
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spelling pubmed-23839142008-05-14 Is the qualitative research interview an acceptable medium for research with palliative care patients and carers? Gysels, Marjolein Shipman, Cathy Higginson, Irene J BMC Med Ethics Research Article BACKGROUND: Contradictory evidence exists about the emotional burden of participating in qualitative research for palliative care patients and carers and this raises questions about whether this type of research is ethically justified in a vulnerable population. This study aimed to investigate palliative care patients' and carers' perceptions of the benefits and problems associated with open interviews and to understand what causes distress and what is helpful about participation in a research interview. METHODS: A descriptive qualitative study. The data were collected in the context of two studies exploring the experiences of care of palliative care patients and carers. The interviews ended with questions about patients' and carers' thoughts on participating in the studies and whether this had been a distressing or helpful event. We used a qualitative descriptive analysis strategy generated from the interviews and the observational and interactional data obtained in the course of the study. RESULTS: The interviews were considered helpful: sharing problems was therapeutic and being able to contribute to research was empowering. However, thinking about the future was reported to be the most challenging. Consent forms were sometimes read with apprehension and being physically unable to sign was experienced as upsetting. Interviewing patients and carers separately was sometimes difficult and not always possible. CONCLUSION: The open interview enables the perspectives of patients and carers to be heard, unfettered from the structure of closed questions. It also enables those patients or carers to take part who would be unable to participate in other study designs. The context is at least as important as the format of the research interview taking into account the relational circumstances with carers and appropriate ways of obtaining informed consent. Retrospective consent could be a solution to enhancing participants control over the interview. BioMed Central 2008-04-24 /pmc/articles/PMC2383914/ /pubmed/18435846 http://dx.doi.org/10.1186/1472-6939-9-7 Text en Copyright © 2008 Gysels et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gysels, Marjolein
Shipman, Cathy
Higginson, Irene J
Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?
title Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?
title_full Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?
title_fullStr Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?
title_full_unstemmed Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?
title_short Is the qualitative research interview an acceptable medium for research with palliative care patients and carers?
title_sort is the qualitative research interview an acceptable medium for research with palliative care patients and carers?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2383914/
https://www.ncbi.nlm.nih.gov/pubmed/18435846
http://dx.doi.org/10.1186/1472-6939-9-7
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