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Being A Parent - Enjoying Family Life: researching a new group for parents and caregivers with significant emotional and interpersonal needs.

Feasibility randomised controlled trial of Being a Parent - Enjoying Family Life: a specialised intervention for parents and caregivers with significant emotional and interpersonal needs.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10950727
Enrollment
72
Registered
2021-09-14
Start date
2021-10-04
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Parents of children aged 2 - 11 who are concerned about their child's behaviour and who themselves have significant emotional and interpersonal difficulties, including those with a diagnosis of personality disorder. Mental and Behavioural Disorders

Interventions

Seventy-two parent/caregiver participants recruited via community pathways will be randomised using a minimisation approach to either: (i) BaP-Enjoying Family Life or (ii) standard Empowering Parents

Sponsors

South London and Maudsley NHS Foundation Trust
Lead Sponsor
King's College London
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Prent inclusion criteria: 1. Primary parental caregiver (self-report of substantial caregiving responsibility), including non-biological caregiver, for index child 2. Aged between 18 - 65 years 3. Persistent emotional and relationship difficulties, assessed by a score of =3 on the Structured Assessment of Personality- Abbreviated Scale 4. Caregiver must have proficient written and spoken English 5. Caregiver must have capacity to provide informed consent to participate. Index Child inclusion criteria: 6. Aged 2 - 11 years 7. Living with parents/caregiver 8. Caregiver reported behavioral difficulties

Exclusion criteria

Exclusion criteria: Parent exclusion criteria: 1. Presence of psychosis, significant brain injury and/or learning disability 2. Engaged in another structured parenting intervention or previous attendance to BaP-Enjoying Family Life/EPEC-Being a Parent group 3. Receiving inpatient mental health treatment 4. Caregiver pregnancy/breastfeeding 5. Family is subject to safeguarding proceedings to remove child from the home Index child exclusion criteria: 6. Presence of neurodevelopmental disorder and/or psychosis 7. Not residing with index parents/caregivers

Design outcomes

Primary

MeasureTime frame
Feasibility outcome: 1. Rate of participant identification and retention, measured through structured record sheets. Clinical outcome: 2. Child behavioural problems, measured using the parent-report Eyberg Child Behaviours Inventory pre, post and at 6 months post intervention

Secondary

MeasureTime frame
Secondary feasibility outcomes are intervention acceptability, measured using a treatment acceptability rating scale administered post intervention. Secondary clinical outcomes are: 1. Parent/caregiver concerns about child behavioural and emotional difficulties, measured using the concerns about my child visual analogue scale at pre, post and 6 month post intervention. 2. Parenting behaviour measured using parent-report Arnold O'Leary Parenting Scale at pre, post and 6 month post intervention. 3. Quality and Quantity of cognitive stimulation and emotional support in the home environment, measured using the Home Observational Measurement of the Environment, an observational and structured interview assessment, at pre, post and 6 month post intervention. 4. Parent/caregiver Satisfaction, measured using the Kansas Parent Satisfaction Scale at pre, post and 6 month post intervention. 5.Parent/caregiver self efficacy, measured using the Brief Parent Self-efficacy Scale at pre, post and 6 month post intervention. 6. Parent/caregiver Reflective function, measured using the Parent reflective functioning questionnaire at pre, post and 6 month post intervention. 7. Parent/caregiver emotional functioning, measured using the Brief Adjustment Scale- 6 at pre, post and 6 month post intervention. 8. Group Cohesion, measured using the Group Cohesiveness Scale at post intervention. Qualitative interviews with a subsample of participants will also be conducted post-intervention to develop a fine grain understanding of trial and intervention experience and evaluate trial and intervention processes.

Countries

England, United Kingdom

Contacts

Public ContactEllie Baker
ellie.baker@kcl.ac.uk+44 (0)203 228 2837

Outcome results

None listed

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