Literature DB >> 17148535

Research with bereaved parents: a question of how not why.

J L Hynson1, R Aroni, C Bauld, S M Sawyer.   

Abstract

BACKGROUND: There is tension around the notion of research with bereaved parents. While it is recognised that the care of children with palliative care needs will only improve with better understanding of parent perspectives, the vulnerability of bereaved parents is equally recognised as a challenge to ethical research. An emerging literature suggests that research can be safely and ethically conducted with bereaved families, if performed sensitively. However, little is known about what research processes might enhance ethical research practice in this field. AIM: To explore the impact of the research process on bereaved parents, and to identify what elements enhance the experience of research participation.
METHODS: This qualitative study used in-depth interview techniques with the bereaved parents of children who had died from a range of conditions.
RESULTS: Interviews took place with 69 parents from 45 eligible families (70% of 64 selected eligible families) of children who had died from a range of chronic conditions. All participants considered the timing and nature of the initial approach by the researchers to be appropriate. The experience for parents was reported to be enhanced by the sensitivity of the initial approach. The use of in-depth qualitative interviews promoted parent empowerment through determining both pace and content of interviews. Although the majority of parents primarily chose to participate for altruistic reasons, many described the research process as personally beneficial.
CONCLUSION: Participating in research was viewed positively by these bereaved parents. Careful attention to the research process in terms of timing, approach and the interviewer's skills were key elements that underpinned a positive experience. The skilled utilisation of in-depth interviewing techniques was perceived to enhance ethical research practice.

Entities:  

Mesh:

Year:  2006        PMID: 17148535     DOI: 10.1177/0269216306072349

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  26 in total

1.  Protecting respondent confidentiality in qualitative research.

Authors:  Karen Kaiser
Journal:  Qual Health Res       Date:  2009-11

2.  Conducting research interviews with bereaved family carers: when do we ask?

Authors:  Brenda Bentley; Moira O'Connor
Journal:  J Palliat Med       Date:  2014-12-17       Impact factor: 2.947

3.  "You helped me keep my head above water"-experience of bereavement research after loss of a loved one in the ICU: insights from the ARREVE study.

Authors:  Alexandra Laurent; Jean Reignier; Amélie Le Gouge; Alice Cottereau; Mélanie Adda; Djillali Annane; Juliette Audibert; François Barbier; Patrick Bardou; Simon Bourcier; Jeremy Bourenne; Alexandre Boyer; François Brenas; Vincent Das; Arnaud Desachy; Jérôme Devaquet; Marc Feissel; Frédérique Ganster; Maïté Garrouste-Orgeas; Guillaume Grillet; Olivier Guisset; Rebecca Hamidfar-Roy; Anne-Claire Hyacinthe; Sebastien Jochmans; Mercé Jourdain; Alexandre Lautrette; Nicolas Lerolle; Olivier Lesieur; Fabien Lion; Philippe Mateu; Bruno Megarbane; Sybille Merceron; Emmanuelle Mercier; Jonathan Messika; Paul Morin-Longuet; Bénédicte Philippon-Jouve; Jean-Pierre Quenot; Anne Renault; Xavier Repesse; Jean-Philippe Rigaud; Ségolène Robin; Antoine Roquilly; Amélie Seguin; Didier Thevenin; Patrice Tirot; Isabelle Vinatier; Elie Azoulay; René Robert; Nancy Kentish-Barnes
Journal:  Intensive Care Med       Date:  2019-08-12       Impact factor: 17.440

4.  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

5.  Evaluation of the burdens and benefits of participation in research by parents of children with life-limiting illnesses.

Authors:  Audrey Hopper; Stacey Crane
Journal:  Nurse Res       Date:  2019-07-18

6.  Compassion and vigilance: investigators' strategies to manage ethical concerns in palliative and end-of-life research.

Authors:  Susan E Hickman; Juliana C Cartwright; Christine A Nelson; Kathleen Knafl
Journal:  J Palliat Med       Date:  2012-06-25       Impact factor: 2.947

7.  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

8.  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 9.  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

10.  Ethical conduct of palliative care research: enhancing communication between investigators and institutional review boards.

Authors:  Amy P Abernethy; Warren H Capell; Noreen M Aziz; Christine Ritchie; Maryjo Prince-Paul; Rachael E Bennett; Jean S Kutner
Journal:  J Pain Symptom Manage       Date:  2014-05-28       Impact factor: 3.612

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