Literature DB >> 12405895

Does research into sensitive areas do harm? Experiences of research participation after a child's diagnosis with Ewing's sarcoma.

Debbie A Scott1, Patricia C Valery, Frances M Boyle, Christopher J Bain.   

Abstract

OBJECTIVE: To investigate family members' experiences of involvement in a previous study (conducted August 1995 to June 1997) following their child's diagnosis with Ewing's sarcoma.
DESIGN: Retrospective survey, conducted between 1 November and 30 November 1997, using a postal questionnaire. PARTICIPANTS: Eighty-one of 97 families who had previously completed an in-depth interview as part of a national case-control study of Ewing's sarcoma. MAIN OUTCOME MEASURES: Participants' views on how participation in the previous study had affected them and what motivated them to participate.
RESULTS: Most study participants indicated that taking part in the previous study had been a positive experience. Most (n = 79 [97.5%]) believed their involvement would benefit others and were glad to have participated, despite expecting and finding some parts of the interview to be painful. Parents whose child was still alive at the time of the interview recalled participation as more painful than those whose child had died before the interview. Parents who had completed the interview less than a year before our study recalled it as being more painful than those who had completed it more than a year before.
CONCLUSIONS: That people suffering bereavement are generally eager to participate in research and may indeed find it a positive experience is useful information for members of ethics review boards and other "gatekeepers", who frequently need to determine whether studies into sensitive areas should be approved. Such information may also help members of the community to make an informed decision regarding participation in such research.

Entities:  

Keywords:  Biomedical and Behavioral Research; Empirical Approach

Mesh:

Year:  2002        PMID: 12405895     DOI: 10.5694/j.1326-5377.2002.tb04921.x

Source DB:  PubMed          Journal:  Med J Aust        ISSN: 0025-729X            Impact factor:   7.738


  10 in total

1.  The Benefits and Burdens of Pediatric Palliative Care and End-of-Life Research: A Systematic Review.

Authors:  Meaghann S Weaver; Kim Mooney-Doyle; Katherine Patterson Kelly; Kathleen Montgomery; Amy R Newman; Christine A Fortney; Cynthia J Bell; Jessica L Spruit; Melissa Kurtz Uveges; Lori Wiener; Cynthia M Schmidt; Vanessa N Madrigal; Pamela S Hinds
Journal:  J Palliat Med       Date:  2019-03-05       Impact factor: 2.947

2.  Participation in Online Research Examining End-of-Life Experiences: Is It Beneficial, Burdensome, or Both for Parents Bereaved by Childhood Cancer?

Authors:  Julia Tager; Haven Battles; Sima Zadeh Bedoya; Cynthia A Gerhardt; Tammi Young-Saleme; Lori Wiener
Journal:  J Pediatr Oncol Nurs       Date:  2019 May/Jun       Impact factor: 1.636

3.  Research participation experiences of parents of children with cancer who were asked about their child's prognosis.

Authors:  Maura E Olcese; Jennifer W Mack
Journal:  J Palliat Med       Date:  2012-02-17       Impact factor: 2.947

Review 4.  Designing and implementing a longitudinal study of children with neurological, genetic or metabolic conditions: charting the territory.

Authors:  Harold Siden; Rose Steele; Rollin Brant; Susan Cadell; Betty Davies; Lynn Straatman; Kimberley Widger; Gail S Andrews
Journal:  BMC Pediatr       Date:  2010-09-20       Impact factor: 2.125

5.  Impact of a genetic diagnosis of a mitochondrial disorder 5-17 years after the death of an affected child.

Authors:  A C Sexton; M Sahhar; D R Thorburn; S A Metcalfe
Journal:  J Genet Couns       Date:  2008-02-12       Impact factor: 2.537

Review 6.  Research governance: ethical issues.

Authors:  Anne Slowther; Petra Boynton; Sara Shaw
Journal:  J R Soc Med       Date:  2006-02       Impact factor: 18.000

7.  "It Can Be Hard But It's Not Bad": Three Questions to Solicit Caregiver Perceptions of Benefits and Burdens to Participating in Pediatric Palliative Care Research.

Authors:  Cheryl Reggio; Catriona Mowbray; Mia K Waldron; Adelaide L Rood; Gabriella Sibilia; Kim Mooney-Doyle; Pamela S Hinds
Journal:  J Palliat Med       Date:  2021-04-23       Impact factor: 2.947

8.  How distressing is it to participate in medical research? A calibration study using an everyday events questionnaire.

Authors:  Keith J Petrie; Kate Faasse; Tracey Anne Notman; Ronan O'Carroll
Journal:  JRSM Short Rep       Date:  2013-09-13

Review 9.  The under reporting of recruitment strategies in research with children with life-threatening illnesses: A systematic review.

Authors:  Briony F Hudson; Linda Jm Oostendorp; Bridget Candy; Victoria Vickerstaff; Louise Jones; Monica Lakhanpaul; Myra Bluebond-Langner; Paddy Stone
Journal:  Palliat Med       Date:  2016-09-08       Impact factor: 4.762

10.  Bereaved parents' experiences of research participation.

Authors:  Ashleigh E Butler; Helen Hall; Beverley Copnell
Journal:  BMC Palliat Care       Date:  2018-11-07       Impact factor: 3.234

  10 in total

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