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An evaluation of Safe Families for Children

The effectiveness of Safe Families for Children in supporting families with children identified as on the edge of care: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN16157843
Enrollment
600
Registered
2015-04-28
Start date
2015-05-18
Completion date
Unknown
Last updated
2020-04-06

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

Conditions

Child emotional and behavioural difficulties and parental anxiety Mental and Behavioural Disorders Behavioural difficulties

Interventions

The SFFC intervention provides support for families who are going through crises. It is a faith-based charity that aims to keep the family together and to reduce the number of children coming into ca

Sponsors

Dartington Social Research Unit
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. At least one of the referred children within a family is aged 10 years or under (child outcome data will be collected for children aged 2 or above as per the validation of the outcome measure) 2. The referred children would be accommodated under Section 20 of The Children Act (1989) if not placed with a SFFC host family (voluntary arrangement) 3. The lead parent/carer contact has parental responsibility for the child(ren) 4. The referred children are perceived to be in need of less than 14 nights care

Exclusion criteria

Exclusion criteria: 1. It is reported by the referring local authority social worker that it would be unsafe for SFFC staff or volunteers to regularly visit the family home 2. It is reported by the referring local authority social worker that any family members (including children) would put SFFC staff or volunteers at risk

Design outcomes

Primary

MeasureTime frame
The study will primarily measure changes in children’s behaviour and emotional functioning and parental anxiety, both from the parents’ perspective (co-primary outcomes). These measures will be administered at baseline, then at follow-up c.8 weeks after randomisation. 1. Strengths and Difficulties Questionnaire- parent report (SDQ: Goodman 1997) (Total Difficulties score – this combines ratings of the child’s difficulties in four domains of functioning: emotional symptoms, conduct problems, hyperactivity, and peer relationship problems.) 2. Hospital Anxiety and Depression Scale (HADS, Snaith & Zigmond, 1983) (Anxiety score)

Secondary

MeasureTime frame
Secondary assessments will include a measure of interpersonal support. In addition, the number of bed nights spent away from home, frequency of re-referral and time lapse between referrals will be measured. The secondary outcome measure will be administered at baseline and at follow-up c.8 weeks after randomisation. The other data will be retrieved c.13 weeks after randomisation (for initial report) and a further 2 time points if the trial period is extended (c.25 weeks and c.50 weeks after randomisation). 1. Interpersonal Support Evaluation List (ISEL, Cohen & Hoberman, 1983). (Total support, tangible support, belonging support, self-esteem support and appraisal support.)

Countries

United Kingdom

Outcome results

None listed

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