Supporting families with infants at risk of sudden unexpected death in infancy Not Applicable
Conditions
Interventions
A realist evaluation study involving before and after mixed methods data collection as follows:
1. Pre-intervention baseline data collection from families completing surveys at approximately 4 and 8 w
Sponsors
University of Bristol
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Health professionals (teams of health visitors, neonatal nurses, midwives and specialist nurses (family nurse partnerships) working with families experiencing poverty. 2. Parents/caregivers of infants, either still pregnant or with infants under 2 weeks old, receiving services from recruited health professional teams, can take part in the evaluation.
Exclusion criteria
Exclusion criteria: 1. Individuals under 16 years of age 2. Anyone who lacks cognitive capacity to consent 3. Anyone unable to complete an interview in English
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safer sleep adherence is measured using infant sleep diaries at 4 weeks and 8 weeks post birth | — |
Secondary
| Measure | Time frame |
|---|---|
| Current secondary outcome measures: 1. Parental self-efficacy is measured using the 13-item two-factor Uppsala Parental Self-Efficacy about Infant Sleep Instrument (UPPSEISI) at 4 weeks and 8 weeks post birth 2. Implementation processes are measured using the 23-item Nomad questionnaires at baseline, 2 months and 4 months Previous secondary outcome measures: 1. Parental self-efficacy is measured using the TOPSE-baby questionnaire at 4 weeks and 8 weeks post birth 2. Implementation processes are measured using the 23-item Nomad questionnaires at baseline, 2 months and 4 months | — |
Countries
England, United Kingdom
Outcome results
None listed