Skip to content

Development and feasibility of a co-produced intervention to enhance parental involvement in facility neonatal care in India, Pakistan and Tanzania

Enhancing parental involvement in the care of sick neonates in India, Pakistan and Tanzania: A Participatory Action Research Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN11273035
Enrollment
180
Registered
2022-08-12
Start date
2023-10-01
Completion date
Unknown
Last updated
2025-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parent partnerships in facility neonatal care to improve outcomes for small and sick newborns Pregnancy and Childbirth

Interventions

A co-production process will be initiated involving representatives from NIHR Unit stakeholders (including local clinicians, policy makers and community leaders) and Community Engagement Groups of loc

Sponsors

Liverpool School of Tropical Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Mother/Caregiver/baby pairs 1. Baby admitted to NNU and expected to remain for >7 days 2. Mother (caregiver) willing to commit to the study intervention (intervention phase only) 3. Mother (caregiver) over 18 years at recruitment Partner/Family member 1. Partner or family member of mother (or caregiver). 2. Over 18 years old at time of recruitment Health workers, service managers, peer supporters 1. Nurses, midwives, doctors directly involved in the delivery of the intervention 2. Peer supporters (parents with prior lived experience) if involved in delivery of the intervention

Exclusion criteria

Exclusion criteria: 1. Multiple births where one only baby received NN care and/or is still living 2. Baby receiving palliative care 3. Baby critically ill (e.g receiving ventilatory/ organ support and/or not expected to survive) 4. Severe congenital abnormality

Design outcomes

Primary

MeasureTime frame
Recruitment and retention of mothers (caregivers) and babies in the study. Recruitment and retention is measured, using the study screening and recruitment log at identification of each eligible participant, approach, recruitment and study completion, withdrawal or loss to follow up.

Secondary

MeasureTime frame
1. Acceptability of the intervention, research and study processes for parents and health workers is assessed using qualitative interviews conducted at the end of the intervention phase, 6-8 weeks following discharge (parents) and at the end of the intervention phase (health workers directly involved in the delivery of the intervention) and a survey questionnaire for all neonatal and maternity staff providing newborn care 2. Characteristics and acceptability of the proposed psychological measures is assessed with mothers/caregivers recruited to the study at the following time points: 2.1. Parental stressor scale: Neonatal intensive care unit (PSS:NICU; measures parental anxiety and stress) baseline (recruitment), immediately prior to baby’s discharge from NNU, 6-8 weeks following discharge 2.2. Edinburgh postnatal depression scale: (assesses depressive symptoms in the postnatal period EPDS) baseline (recruitment), immediately prior to baby’s discharge from NNU, 6-8 weeks following discharge

Countries

India, Pakistan, Tanzania

Contacts

Public ContactTracey Mills
tracey.mills@lstmed.ac.uk+44 151 8321694

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026