Challenging Behaviour Clinical Trial
Official title:
Clinical and Cost Effectiveness of a Parent Mediated Intervention to Reduce Challenging Behaviour in Pre-schoolers With Moderate to Severe Learning Disability: a Randomised Controlled Trial
NCT number | NCT03086876 |
Other study ID # | 15/162/02 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 1, 2017 |
Est. completion date | March 31, 2022 |
Verified date | April 2022 |
Source | University College, London |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Children with intellectual disabilities are likely to present with challenging behaviour. Parent mediated interventions have shown utility in influencing child behaviour, although there is a paucity of UK research into challenging behaviour interventions in this population. NICE guidelines favour Stepping Stones Triple P (SSTP) as a challenging behaviour intervention and this trial aims to evaluate its clinical and cost effectiveness in preschool children with moderate to severe intellectual disabilities.The trial launched in 2017 at four sites across England, with the aim of recruiting 258 participants (aged 30-59 months). The Intervention Group receive nine weeks of SSTP parenting therapy (six group sessions and three individualised face to face or telephone sessions) in addition to Treatment as Usual (TAU) whilst the TAU group receive available services in each location. Both study groups undergo the study measurements at baseline and at four and twelve months. Outcome measures include parent reports and structured observations of behaviour. Service use and health related quality of life data is also being collected to carry out a cost effectiveness and utility evaluation. Findings from this study will inform policy regarding interventions for challenging behaviour in young children with moderate to severe intellectual disabilities.
Status | Completed |
Enrollment | 261 |
Est. completion date | March 31, 2022 |
Est. primary completion date | December 17, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Months to 59 Months |
Eligibility | Inclusion Criteria: - Age: Parents 18 years or over; Child aged 30-59 months at identification; - Child has moderate to severe intellectual disability (parent reported Adaptive Behaviour Assessment System (ABAS) General Adaptive Functioning 20-69); - Written informed consent by parent/caregiver; - Reports of challenging behaviour over a 6-month period but no less than 2 months. Exclusion Criteria: - Child has mild, profound or no LD on parent reported ABAS; - Parent/carer has insufficient English language to complete study questionnaires; - Another sibling is taking part in the study. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Blackpool Teaching Hospitals NHS Foundation Trust | Blackpool | |
United Kingdom | Central and North West London NHS Foundation Trust | London | |
United Kingdom | Guy's and St Thomas NHS Foundation Trust | London | |
United Kingdom | Northumberland, Tyne and Wear NHS Foundation Trust | Newcastle |
Lead Sponsor | Collaborator |
---|---|
University College, London |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Child Behaviour Check List (CBCL) | Children's challenging behaviour will be measured at 12 months post randomisation using the parent completed preschool Child Behaviour Checklist (CBCL) | 12 months | |
Secondary | Revised Family Observation Schedule (FOS-RIII) | Direct observations will be carried out by masked research assistants using the Revised Family Observation Schedule (FOS-RIII) as an objective measure of challenging behaviour | 12 months | |
Secondary | Child Behaviour Checklist Caregiver-Teacher Report Forms (C-TRF) | Caregiver (not parent) reported child behaviour (Child Behaviour Checklist Caregiver-Teacher Report Forms; C-TRF). Most children in the sample age range will have additional care outside the parental home allowing us to have additional perspectives on the child's behaviour. | 12 months | |
Secondary | General Health Questionnaire (GHQ) | We will measure parent psychiatric morbidity using the General Health Questionnaire. This well established instrument will provide additional information about common psychiatric morbidity in the parent. | 12 months | |
Secondary | Questionnaire on Resources and Stress (QRS-F short form) | Parent stress will be measured using the Questionnaire on Resources and Stress QRS-F short form. This validated questionnaire measures stress in caregivers of chronically ill or children with LD. | 12 months | |
Secondary | Caregiving Problem Checklist-Difficult Child Behaviour | Frequency of behaviour severity during care-giving tasks will be measured using the Caregiving Problem Checklist-Difficult Child Behaviour. This measure assesses the frequency of difficult child behaviour when the parent is completing care-giving tasks. | 12 months | |
Secondary | Parenting Sense of Competence Scale (PSOC) | Satisfaction and efficacy as parent will be measured using the Parenting Sense of Competence Scale, PSOC. The Parenting Sense of Competence scale measures parent rated competence on the dimensions of Satisfaction and Efficacy as a parent. | 12 months | |
Secondary | Child and Adolescent Service Use Schedule (CA-SUS) | Health and social care service use will be measured using the Child and Adolescent Service Use Schedule, CA-SUS. A modified version of the Child and Adolescent Service Use Schedule will be used in the trial. | 12 months | |
Secondary | Pediatric Quality of Life (PedsQL) | Health related quality of life will be measured using the Pediatric Quality of Life, PedsQL. The measure covers Physical, Emotional, Social, School Functioning domains. It contains a parent proxy report for children aged 2 years and over. It will be used in the study to derive QALYS for the health economic evaluation. | 12 months | |
Secondary | EuroQoL (EQ-5D) | Health related quality of life in the parent/other caregiver will be measured using the EQ-5D; 47. This self-completed questionnaire will capture parental and caregiver perspective on his/her health status which will be used in the economic evaluation. | 12 months | |
Secondary | Client Satisfaction Questionnaire (CSQ) | Parent intervention acceptability will be measured using the Client Satisfaction Questionnaire. The questionnaire will allow parents to provide feedback about the intervention by commenting on their satisfaction with and experience of the intervention, including ease of use, format and helpfulness. It has been specifically developed for research in SSTP. | 4 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
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