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Supporting young mothers (aged 14-25) in the first two years of life: a randomized controlled trial of the NSPCC UK Minding the Baby Home Visiting Programme

Supporting young mothers (aged 14-25) in the first two years of life: a randomized controlled trial of the NSPCC UK Minding the Baby Home Visiting Programme

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN08678682
Enrollment
200
Registered
2014-04-03
Start date
2014-04-14
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

Topic: Reproductive health and childbirth

Interventions

1. Minding the Baby: This is an intensive home visiting intervention in which mothers are visited weekly by a trained practitioner in the first year, and two-weekly in the second. 2. T

Sponsors

University College London (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Primparous 2. Age 19 or under at the baby's conception OR age between 20 and 25 and in receipt of means-tested benefits Target Gender: Female; Upper Age Limit 25 years ; Lower Age Limit 14 years

Exclusion criteria

Exclusion criteria: 1. Mothers with a psychotic illness 2. Substance abuse disorders/chronic drug dependence 3. Those with profound or severe learning disabilities 4. Those parents with a life-threatening illness 5. Parents whose child is expected to be born with a life threatening illness or profound disability 6. The mother has been screened for participation in a Family nurse Partner Service (See A-29) 7. Non-English speaking These exclusions have been made because families need to be able to understand and give informed consent, participate in treatment, and understand and complete all research questionnaires and assessments. Not all clinicians providing the interventions for the study are able to work with interpreters when working with non-English speaking families. Also, most of the research instruments have not been validated in other languages. The programme is believed to be inappropriate for mothers with very severe mental illness or substance abuse disorders.

Design outcomes

Primary

MeasureTime frame
Parental sensitivity; Timepoint(s): 12 months, 24 months

Secondary

MeasureTime frame
1. Attachment security; Timepoint(s): 12, 24months 2. Child behavioural problems; Timepoint(s): 24 months 3. Child cognitive/language development; Timepoint(s): 24 months 4. Incidences of child abuse and neglect; Timepoint(s): 12, 24 months 5. Maternal mental health; Timepoint(s): Baseline, 12 and 24 months 6. Postponed childbearing; Timepoint(s): 24 months 7. Service cost evaluation; Timepoint(s): 24 months

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 12, 2026