A Feasibility Randomised Control Trial to Evaluate Early Perinatal Bereavement Counselling for Parents Who Have Experienced a Perinatal Death (PEARL-C)

University of Manchester

Status: Not yet enrolling

Conditions: Grief; Perinatal Death; Psychological; Stillbirth

Treatments: Other: Bereavement Counselling; Other: Usual bereavement care

Study type: Interventional

Funder types: Other

Identifiers

NCT07494760

348762

Details and patient eligibility

About

The goal of this feasibility randomised control trial is to determine if a trial to evaluate perinatal bereavement counselling for parents who have experienced a perinatal death is feasible. The main question it aims to answer is:

• Is a trial to evaluate access to perinatal bereavement counselling feasible?

Researchers will compare the intervention group (parents who have received counselling) to the control group (parents who have not received counselling) to see if there are differences in measurements of parents' grief and psychological symptoms.

• Participants allocated to the intervention and control group will receive usual bereavement care from the perinatal bereavement team at the hospital
• Parents allocated to the intervention group will receive counselling
• Parents will complete validated psychometric questionnaires about their levels of perinatal grief, psychological distress, depression, and quality of life
• Parents in the intervention group will be asked a series of open-ended written questions about their experience of participating in the trial
• Healthcare professionals who have been involved with delivery of the intervention/referrals will be interviewed about their experience of the trial.

Full description

In 2022, there were 4 stillbirths and 2.9 neonatal deaths for every 1,000 babies born in England and Wales. Despite the frequency of perinatal deaths, currently, there is no consistent provision of perinatal bereavement counselling for parents after stillbirth. This single-centre study aims to determine whether a randomised control trial to evaluate perinatal bereavement counselling is feasible. It will provide essential information to underpin a larger study which will give a more definite answer about the benefit of perinatal counselling. The larger study will inform national clinical practice guidelines by providing evidence for policymakers and professionals to make recommendations about whether perinatal counselling should be offered following stillbirth or neonatal death. The investigators will recruit mothers and partners from Manchester University National Health Service (NHS) Foundation Trust on the bereavement suite on the birth centre at Wythenshawe Hospital (where there is currently no perinatal bereavement counselling service). Parents will be eligible if they have experienced the death of a baby within the maternity setting at Wythenshawe Hospital. The investigators aim for 13 participants to receive the intervention and 13 participants to be allocated to the control group. Participants allocated to the intervention and control group will receive usual bereavement care from the perinatal bereavement team at the hospital; parents allocated to the intervention group will also receive 6-8 sessions of counselling over a 3-4-month period from a trained bereavement counsellor. Participants will complete validated psychometric questionnaires about their levels of perinatal grief, psychological distress, depression, and quality of life which will be administered at 2 months postnatal (before counselling begins), at 7-9 months postnatal (after counselling ends), and 12 months postnatal (follow-up). Parents in the intervention group will also answer (in writing) a series of open-ended questions about their experience of engaging with the trial on their 7-9 month questionnaire. The investigators will also interview approximately 4 healthcare professionals who have been involved with delivery of the intervention/referrals during the trial about their experience of the trial.

Enrollment: 26 estimated patients

Sex: All

Ages: 16+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Women and partners of women who have had a late fetal loss (from 16 weeks), stillbirth or neonatal death within the maternity unit at Wythenshawe Hospital.
• For the qualitative interviews, healthcare professionals who have been involved with referrals to the intervention and/or the delivery of the intervention

Exclusion criteria

• Less than 16 years of age
• Anyone who lacks the capacity to consent
• Inability to read English (interpreters will be provided for counselling sessions and interviews if needed).

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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26 participants in 2 patient groups

Bereavement Counselling

Experimental group

Description:

Bereavement counselling from a specialist bereavement counsellor

Treatment:

Other: Usual bereavement care

Other: Bereavement Counselling

Usual bereavement care

Active Comparator group

Description:

Routine care provided by the bereavement team

Treatment:

Other: Usual bereavement care