Bereaved parents' experiences of research participation

Article indépendant

BUTLER, Ashleigh E. | HALL, Helen | COPNELL, Beverley

BACKGROUND: As understandings of the impacts of end-of-life experiences on parents' grief and bereavement increase, so too does the inclusion of bereaved parents into research studies exploring these experiences. However, designing and obtaining approval for these studies can be difficult, as guidance derived from bereaved parents' experiences of the research process are limited within the current literature. METHODS: We aimed to explore bereaved parents' experiences of research participation in a larger grounded theory study exploring experiences of the death of a child in the paediatric intensive care unit. Data were obtained during follow-up phone calls made to 19 bereaved parents, five of whom provided data from their spouse, 1 week after their participation in the study. Participants were asked to reflect on their experiences of research participation, with a focus on recruitment methods, timing of research contact, and the location of their interview. Parents' responses were analysed using descriptive content analysis. RESULTS: Our findings demonstrate that despite being emotionally difficult, parents' overall experiences of research participation were positive. Parents preferred to be contacted initially via a letter, with an opt in approach viewed most favourably. Most commonly, participants preferred that research contact occurred within 12-24 months after their child's death, with some suggesting contact after 6 months was also appropriate. Parents also preferred research interviews conducted in their own homes, though flexibility and parental choice was crucial. CONCLUSIONS: Findings from this study offer further insight to researchers and research review committees, to help ensure that future studies are conducted in a way that best meets the unique needs of bereaved parents participating in research.

https://bmcpalliatcare.biomedcentral.com/track/pdf/10.1186/s12904-018-0375-4

Voir la revue «BMC palliative care, 17»

Autres numéros de la revue «BMC palliative care»

Consulter en ligne

Suggestions

Du même auteur

Bereaved parents' experiences of research par...

Article indépendant | BUTLER, Ashleigh E. | BMC palliative care | n°1 | vol.17

BACKGROUND: As understandings of the impacts of end-of-life experiences on parents' grief and bereavement increase, so too does the inclusion of bereaved parents into research studies exploring these experiences. However, designin...

When a child dies in the PICU : practice reco...

Article indépendant | BUTLER, Ashleigh E. | Pediatric critical care medicine:

Objectives: Around the world, the PICU is one of the most common sites for hospitalized children to die. Although ensuring the best possible care experience for these children and their families is important, clear recommendations...

When a child dies in the PICU : practice reco...

Article indépendant | BUTLER, Ashleigh E. | Pediatric critical care medicine:

Objectives: Around the world, the PICU is one of the most common sites for hospitalized children to die. Although ensuring the best possible care experience for these children and their families is important, clear recommendations...

De la même série

Learning from experience : does providing end...

Article indépendant | MEIER, Clément | BMC palliative care | n°1 | vol.24

BACKGROUND: Despite the critical role of health literacy in utilizing palliative care and engaging in advance care planning, limited research exists on the determinants of end-of-life health literacy. This study investigates the a...

A relational approach to co-create advance ca...

Article indépendant | PHENWAN, Tharin | BMC palliative care | n°1 | vol.24

BACKGROUND: Discussing Advance Care Planning (ACP) with people living with dementia (PwD) is challenging due to topic sensitivity, fluctuating mental capacity and symptom of forgetfulness. Given communication difficulties, the pre...

Determining timeframes to death for imminentl...

Article indépendant | O'CONNOR, Tricia | BMC palliative care | n°1 | vol.24

BACKGROUND: Clinicians are frequently asked 'how long' questions at end-of-life by patients and those important to them, yet predicting timeframes to death remains uncertain, even in the last weeks and days of life. Patients and f...

Don't assume, ask! A focus group study on end...

Article indépendant | BRUUN, Andrea | BMC palliative care | n°1 | vol.24

BACKGROUND: People with intellectual disabilities are less likely to have access to palliative care, and the evidence shows that their deaths are often unanticipated, unplanned for, and poorly managed. Within the general populatio...

Future directions of spiritual care where spi...

Article indépendant | MEEPRASERTSAGOOL, Nattawan | BMC palliative care | n°1 | vol.24

INTRODUCTION: Spiritual care is a fundamental aspect of palliative care, addressing the emotional, existential, and spiritual needs of patients facing life-threatening illnesses. However, in Thailand, the integration of spiritual ...

Chargement des enrichissements...