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Managing repetitive behaviours parent group study

Managing repetitive behaviours: a clinical and cost effectiveness trial of a parent group intervention to manage restricted and repetitive behaviours in young children with autism spectrum disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15550611
Enrollment
250
Registered
2018-08-07
Start date
2018-09-01
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Repetitive behaviours in children with autism spectrum disorder Mental and Behavioural Disorders Childhood autism

Interventions

This is a multicentre, 2 arm randomised control trial with 3 sites across England and Scotland. Patients will be randomised 1:1 to receive either the MRB intervention or psychoeducation group (Learni

Sponsors

Northumberland, Tyne and Wear NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Current inclusion criteria as of 21/08/2019: Parents/carers aged 18 years and over who: 1. Have a child aged between 3 years and 9 years and 11 months at the time of consent with a clinical diagnosis of Autism or Autism Spectrum Disorder 2. Have sufficient spoken and written English to: 2.1. Provide written informed consent 2.2. Complete the assessments including being able to identify one or more challenging RRB 2.3. Participate in the group-based intervention 3. Are willing to be randomised and attend all the group sessions for the allocated arm of the study 4. Agree to maintain their child’s current medication regime up to 24 weeks (unless change is advised by child’s clinician) 5. Agree not to participate in any other trials while involved in the trial up to 24 weeks Previous inclusion criteria: Parents/carers aged 18 years and over who: 1. Have a child aged between 3 years and 7 years and 11 months at the time of consent with a clinical diagnosis of Autism or Autism Spectrum Disorder 2. Have sufficient spoken and written English to: 2.1. Provide written informed consent 2.2. Complete the assessments including being able to identify one or more challenging RRB 2.3. Participate in the group-based intervention 3. Are willing to be randomised and attend all the group sessions for the allocated arm of the study 4. Agree to maintain their child’s current medication regime 5. Agree not to participate in any other trials while involved in the trial up to 24 weeks

Exclusion criteria

Exclusion criteria: 1. Parent and child currently taking part in another parent group-based intervention 2. Parent with a current severe learning disability or a severe disabling mental illness that interferes with ability to take part in group-based intervention trial 3. Sibling is taking part in this study

Design outcomes

Primary

MeasureTime frame
Improvement or no improvement at 24 weeks, based on the clinical global impression of improvement (CGI-I)

Secondary

MeasureTime frame
Primary Economic Outcome Measure Cost per additional child achieving at least the target improvement in CGI-I scale will be calculated in each pathway Secondary Child Outcome Measures 1. Restrictive Repetitive Behaviours (RRB), measured using Target Behaviour Vignette at baseline, Week 10, Week 24 and Week 52 2. RRB, measured using Repetitive Behaviour Questionnaire - 2 (RBQ-2) at baseline, Week 10, Week 24 and Week 52 3. RRB, measured using Teacher Repetitive Behaviour Questionnaire 2 (Teacher RBQ-2) at baseline, Week 10, Week 24 and Week 52 4. Adaptive functioning, measured using Vineland Adaptive Behaviour Scales III (VABS III) at baseline and Week 24 Parent Outcome Measures 1. Behaviours typically exhibited by children with ASD, measured using parent self-efficacy questionnaire at baseline, Week 10, Week 24 and Week 52 2. Parenting stress specific to core and co-morbid symptoms of ASD, measured using Autism Parenting Stress Index (APSI) at baseline, Week 10, Week 24 and Week 52 3. Wellbeing, measured using Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS) at baseline, Week 24 and Week 52 Secondary Family Outcome Measures Autism Family Experience Questionnaire (AFEQ) at baseline, Week 24 and Week 52 Secondary Economic Outcome Measures 1. Healthcare resources which are used by the children, measured using resource use questionnaire at baseline, Week 24 and Week 52. This will be calculated to result in an average cost of services per pathway 2. Costs and time lost to travel, measured using time and travel questionnaire at baseline 3. Health-related quality of life of caregivers reported per child, measured using EQ-5D-5L questionnaire at baseline, Week 24 and Week 52 4. Health-related quality of life of the child with RRB, measured using CHU9D proxy version at baseline, Week 24 and Week 52 Updated 04/04/2019: VABS II changed to VABS III.

Countries

England, Scotland, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 23, 2026