Feasibility of a co-produced intervention to improve support after stillbirth and neonatal death in India and Pakista
- Conditions
- Stillbirth or neonatal death in current pregnancyPregnancy and Childbirth
- Registration Number
- ISRCTN42868391
- Lead Sponsor
- iverpool School of Tropical Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- All
- Target Recruitment
- 80
Women:
1. Immediate postnatal period
2. Experienced stillbirth (baby born at or after 28 weeks gestation with no signs of life) or early neonatal death (live birth, died 0-6 days before discharge) in the included facilities, within the study recruitment periods
3. Over 18 years at time of recruitment
Partners/family members/friends:
1. Identified by women consented to take part in the study during the intervention period only; they will be approached via the woman after she has agreed (a partner’s etc unwillingness to participate will not affect the woman’s continued
participation)
2. Aged 18 years or over, at the time of recruitment
Health workers:
1. Midwives/nurses, doctors, support staff and others directly involved in the delivery of the study intervention or who provide care or services to women after stillbirth in facilities.
2. Survey only: Health workers involved providing or managing maternity or neonatal services, but not previously directly involved in the research
1. Women who are unable to give consent
2. Multiple births only where one baby survived the early neonatal period (women)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method