Evaluation of CO-OP for Adolescents With Mild Intellectual Disability
- Conditions
- Intellectual Disability, Mild
- Registration Number
- NCT06691698
- Lead Sponsor
- Örebro University, Sweden
- Brief Summary
Intellectual disability (ID) affects a person throughout life and includes difficulties to manage what is expected in everyday life based on age. One difficulty is to create strategies for and solve problems related to everyday occupations. Treatment options with good evidence to enhance occupational performance for persons with ID are limited. The Cognitive Orientation to Daily Occupational Performance (CO-OP) is an approach with good evidence within other diagnostic groups, i.e. adolescents with cerebral palsy. CO-OP has a unique person-centered approach where the person chooses his/her own goals and creates his/her own strategies to reach them. Initial research shows potential for CO-OP with adolescents with ID, although due to scientific flaws there is still a lack of evidence regarding feasibility and effectiveness for adolescents with ID. Based on the results with other diagnostic groups and clinical knowledge and experience, CO-OP can be assumed to be feasible and effective for adolescents with ID and to have a long term effect transferred to everyday life in a way other treatment options do not.
The aim of the project is to describe and evaluate CO-OP for adolescents with mild ID. Participants will be adolescents aged 13-17 and their parents. The project is designed as a feasibility study with two qualitative, one quantitative and one mixed method data collection. The quantitative data will be ordinal and nominal data from observational and self-assessment assessments. The mixed methods include comparison between filmed sessions and the CO-OP manual, use of field notes to analyse fidelity and needs for adaptations, and comparison between the CO-OP manual and policy documents. The qualitative outcome will be experiences by the adolescents and perceptions of CO-OP by parents.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 60
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Change in Canadian Occupational Performance Measure - performance Baseline, up to 4 weeks post intervention and 6 months post intervention Self-rated occupational performance in four chosen goal activities, rated 1-10
Change in Canadian Occupational Performance Measure - satisfaction Baseline, up to 4 weeks post intervention and 6 months post intervention Self-rated satisfaction with performance in four chosen goal activities, rated 1-10
Change in Performance Quality Rating Scale - occupational performance quality Baseline, up to 4 weeks post intervention and 6 months post intervention Observed performance quality during performing four chosen goal activities thas is filmed and rated 1-10.
- Secondary Outcome Measures
Name Time Method Change in General Self-Efficacy Scale - self-efficacy Baseline, up to 4 weeks post intervention and 6 months post intervention Self-rated self-efficacy, 10 statements rated 1-4.
Experiences of CO-OP as a patient - qualitative Up to 4 weeks post intervention and 6 months post intervention Qualitative semi-structured interviews analyzed using qualitative content analysis.
Perceptions of CO-OP as a parent of a patient - qualitative Up to 4 weeks post intervention and 6 months post intervention Qualitative semi-structured interviews analyzed using phenomenographic analysis
Trial Locations
- Locations (2)
Region Skåne
🇸🇪Kristianstad, Skåne, Sweden
Region Värmland
🇸🇪Karlstad, Värmland, Sweden