“This Kind of Thing is Part of His Legacy”: Bereaved Parents’ Experiences of Participating in Interview-Based Research

<b><i>Background:</i></b> Every year, a significant number of parents/caregivers experience the loss of a child, many of whom have received palliative care services. The resultant consequences of grief on their physical and psychological well-being can be significant. Little is known about bereaved parents/caregivers experience with or perceptions about participating in bereavement-focused research. <b><i>Objective:</i></b> To explore bereaved parents' perceptions of participating in three research studies about their loss experiences and legacy perceptions. <b><i>Design:</i></b> A retrospective secondary analysis was conducted using qualitative and archival data drawn from three prior studies. <b><i>Setting/Subjects:</i></b> Participants included parents/caregivers of 44 children (ages from birth to 18 years) who died between 2000 and 2020 at a freestanding academic children's hospital in the United States. <b><i>Measurements:</i></b> Transcripts from semi-structured interviews and documentation of email communications were analyzed using an inductive coding approach grounded in psychological phenomenology. <b><i>Results:</i></b> Participant experiences of and motivations for participating in bereavement-related research were organized into two themes: 1) a means of extending the child's legacy and 2) an avenue for self-expression and gratitude. None of the participants across studies indicated any discomfort in, dissatisfaction with, or ill feelings toward bereavement research involvement. <b><i>Conclusions:</i></b> Bereaved parents/caregivers described their research participation in personally meaningful and altruistic ways and reported gratitude for their involvement in and the focus of the research. With careful attention to bereaved parent/caregiver participant needs and preferences, it is possible to produce impactful family-centered palliative care research that can improve anticipatory and bereavement service provision.

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Publication Details

Journal
Journal of Palliative Medicine
Published
2025-04-07
DOI
https://doi.org/10.1089/jpm.2024.0547
Primary Topic
Data Analysis and Archiving
Type
article
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article

“This Kind of Thing is Part of His Legacy”: Bereaved Parents’ Experiences of Participating in Interview-Based Research

Ananya Terala, Mellita Jones, Jessika C. Boles
Journal of Palliative Medicine
Data Analysis and Archiving
article

“This Kind of Thing is Part of His Legacy”: Bereaved Parents’ Experiences of Participating in Interview-Based Research

Ananya Terala, Mellita Jones, Jessika C. Boles
article en

Abstract

<b><i>Background:</i></b> Every year, a significant number of parents/caregivers experience the loss of a child, many of whom have received palliative care services. The resultant consequences of grief on their physical and psychological well-being can be significant. Little is known about bereaved parents/caregivers experience with or perceptions about participating in bereavement-focused research. <b><i>Objective:</i></b> To explore bereaved parents' perceptions of participating in three research studies about their loss experiences and legacy perceptions. <b><i>Design:</i></b> A retrospective secondary analysis was conducted using qualitative and archival data drawn from three prior studies. <b><i>Setting/Subjects:</i></b> Participants included parents/caregivers of 44 children (ages from birth to 18 years) who died between 2000 and 2020 at a freestanding academic children's hospital in the United States. <b><i>Measurements:</i></b> Transcripts from semi-structured interviews and documentation of email communications were analyzed using an inductive coding approach grounded in psychological phenomenology. <b><i>Results:</i></b> Participant experiences of and motivations for participating in bereavement-related research were organized into two themes: 1) a means of extending the child's legacy and 2) an avenue for self-expression and gratitude. None of the participants across studies indicated any discomfort in, dissatisfaction with, or ill feelings toward bereavement research involvement. <b><i>Conclusions:</i></b> Bereaved parents/caregivers described their research participation in personally meaningful and altruistic ways and reported gratitude for their involvement in and the focus of the research. With careful attention to bereaved parent/caregiver participant needs and preferences, it is possible to produce impactful family-centered palliative care research that can improve anticipatory and bereavement service provision.

Journal of Palliative MedicineVol. 28(8)
Vanderbilt University (US), Children's Hospital Colorado (US), Monroe Carell Jr. Children's Hospital (US), University of Colorado Denver (US)
Openalex Percentile: Top 91%
Data Analysis and Archiving
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