SAFE, a new therapeutic intervention for families of children with autism: a randomised controlled feasibility trial.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
31 12 2020
Historique:
entrez: 1 1 2021
pubmed: 2 1 2021
medline: 15 5 2021
Statut: epublish

Résumé

To establish the feasibility of a definitive randomised controlled trial of Systemic Autism-related Family Enabling (SAFE), an intervention for families of children with autism. A randomised, controlled, multicentred feasibility study. Participants were identified from three National Health Service (NHS) diagnosing centres in Plymouth and Cornwall and a community pathway. 34 families of a child with a diagnosis of autism severity level 1 or 2 between 3 and 16 years. Four families were lost to follow-up. SAFE is a manualised five-session family therapy-based intervention delivered over 16 weeks and designed for families of children with autism. SAFE involves families attending five 3-hour sessions led by systemic practitioners. The proposed primary outcome measure was the Systemic CORE 15 (SCORE-15). Proposed secondary outcome measures: Patient Health Questionnaire-Somatic Anxiety Depressive Symptoms, the Coding of Attachment-Related Parenting for use with children with Autism, the Child Behaviour Checklist (CBCL), the Reflective Functioning Questionnaire (RFQ) and the Caregiving Helplessness Questionnaire. Outcome measures were collected at baseline and 24 weeks post randomisation. All primary caregivers retained in the study completed the SCORE-15 at both time points. 34 of the target of 36 families were recruited and 88% of families were retained. Training for therapists was effective. Feedback revealed willingness to undergo randomisation. There was 100% attendance at appropriate sessions for core family members. The SCORE-15 showed reduction in scores for families receiving SAFE compared with controls suggesting positive change. Qualitative data also revealed that families found the study acceptable and families receiving SAFE experienced positive change. Feedback indicated that the SCORE-15 should be retained as a primary measure in a future trial, but secondary measures should be reduced. This study indicates that a larger trial of SAFE is feasible. Findings suggest that SAFE can address current gaps in recommended care, can be confidently delivered by NHS staff and has potential as a beneficial treatment. ISCTRN83964946 and IRAS213527.

Identifiants

pubmed: 33384385
pii: bmjopen-2020-038411
doi: 10.1136/bmjopen-2020-038411
pmc: PMC7780715
doi:

Banques de données

ISRCTN
['ISCTRN83964946']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e038411

Subventions

Organisme : Department of Health
ID : PB-PG-0815-20058
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: Contributors are coapplicants or employed research staff on the SAFE project, which receives funds from both NIHR and Autistica. RD holds joint Intellectual Property rights for the SAFE intervention with the University of Plymouth.

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Auteurs

Rebecca McKenzie (R)

Institute of Education, University of Plymouth, Plymouth, UK rebecca.mckenzie@plymouth.ac.uk.

Rudi Dallos (R)

Department of Clinical Psychology, University of Plymouth, Plymouth, UK.

Jacqui Stedmon (J)

Department of Clinical Psychology, University of Plymouth, Plymouth, UK.

Helen Hancocks (H)

Peninsula Clinical Trials Unit, University of Plymouth, Plymouth, UK.

Patricia Jane Vickery (PJ)

Peninsula Clinical Trials Unit, University of Plymouth, Plymouth, UK.

Andy Barton (A)

South West Research Design Service, Plymouth, UK.

Tara Vassallo (T)

Institute of Education, University of Plymouth, Plymouth, UK.

Craig Myhill (C)

Institute of Education, University of Plymouth, Plymouth, UK.

Jade Chynoweth (J)

Medical Statistics, University of Plymouth, Plymouth, UK.

Paul Ewings (P)

Research Office, Research Design Service, Taunton, UK.

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Classifications MeSH