Modified Delphi for Genomic Bereavement Care
NCT05655741 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 56
Last updated 2023-04-05
Summary
It is estimated that 1 in 4 pregnancies end in loss, be these early miscarriages, ectopic pregnancies, or later intrauterine losses for any reason. Genomics is a major part of pregnancy loss, and clinicians want to offer the best and most appropriate test available to women and their families, whilst ensuring that there is equity in the access to this testing, so that no family goes through a loss without the right support and information. Whilst there is limited information to inform professionals as to how to incorporate genomics into bereavement care there is a need to identify current expert consensus as to how this should be performed, in order to make recommendations for best practice.
Conditions
- Fetal Anomaly
- Bereavement
- Genetic Disease
Interventions
- OTHER
-
Questionnaire
Participants will be asked to complete a series of 3 questionnaires that will be used to gain insight into the current expert consensus for Genomic Bereavement care for Pregnancy Loss. The 2nd and 3rd Questionnaire will be modified from the first to try to generate consensus, depending on the answers from the previous round.
Sponsors & Collaborators
-
Genomic Medicine Services Alliance
collaborator UNKNOWN -
The Leeds Teaching Hospitals NHS Trust
lead OTHER
Principal Investigators
-
Abigail Hyland, MBBS · Leeds Teaching Hospitals Trust
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-10-28
- Primary Completion
- 2023-03-17
- Completion
- 2023-03-31
Countries
- United Kingdom
Study Locations
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