Using CO-OP to help adolescents with mild intellectual disability
Evaluation of The Cognitive Orientation to Daily Occupational Performance (CO-OP) Approach for Adolescents With Mild Intellectual Disability
This study is testing a program called CO-OP to see if it can help teenagers with mild intellectual disabilities set and reach personal goals over ten weeks.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 13 Years to 17 Years |
| Sex | All |
| Sponsor | Örebro University, Sweden Academic / other |
| Locations | 2 sites (Kristianstad, Skåne County and 1 other locations) |
| Trial ID | NCT06691698 on ClinicalTrials.gov |
What this trial studies
This study evaluates the Cognitive Orientation to Daily Occupational Performance (CO-OP) approach for adolescents aged 13-17 with mild intellectual disability. Participants will select personal goals and develop strategies to achieve them over a ten-week intervention period. The study aims to assess the feasibility and effectiveness of CO-OP in enhancing occupational performance in this population, building on initial research that suggests potential benefits. The intervention will involve weekly meetings and support from a parent or significant other.
Who should consider this trial
Good fit: Ideal candidates are adolescents aged 13-17 diagnosed with mild intellectual disability who are motivated to set and achieve personal goals.
Not a fit: Patients with movement-related diagnoses, ADHD, autism spectrum disorder, or those requiring language interpretation will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve daily functioning and quality of life for adolescents with mild intellectual disability.
How similar studies have performed: Initial research has shown potential for CO-OP in other diagnostic groups, but this specific application for adolescents with mild intellectual disability is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Study I-II Inclusion criteria * 13-17 years * Diagnosed mild intellectual disability * Motivation to reach self-selected goals * Ability to identify those goals * Possibility to meet once a week for ten weeks * Access to a parent or significant other for support during intervention Exclusion criteria: * Movement related diagnosis (i.e. cerebral palsy or neuro muscular diseases) * Diagnosed attention deficit hyperactivity disorder/attention deficit disorder (ADHD/ADD) or autism spectrum disorder * Progressive diagnoses * Need for language interpreting * Need for alternative and augmentative communication (i.e. pictures or signs). Study III Inclusion criteria: * 13-17 years * Diagnosed mild intellectual disability * Completed CO-OP intervention or at lest half way trough the intervention * Opportunity to meet physically for an interview with in a month post and 6 months post intervention. * CO-OP intervention done with high fidelity to CO-OP format with a CO-OP therapist that has written field notes, preferrably recruited from study I-II. Exclusion criteria: * Movement related diagnosis (i.e. cerebral palsy or neuro muscular diseases) * Diagnosed attention deficit hyperactivity disorder/attention deficit disorder (ADHD/ADD) or autism spectrum disorder * Progressive diagnoses * Need for language interpreting * Need for alternative and augmentative communication (i.e. pictures or signs). Study IV Inclusion criteria: * Parents with legal guardianship that lives full- or part time with an adolescent reaching the inclusion criteria for study I who has completed CO-OP within or out of the project * Opportunity to meet physically for an interview with in a month post and 6 months post the adolescent's completed, or at least half way through, CO-OP intervention. Exclusion criteria: * Need for language interpreting * Need for alternative and augmentative communication (i.e. pictures or signs) * Irregular and brief living with the adolescent comparable to less than half-time and therefore does not observe the adolescent's occupational performance enough to answer the interview questions.
Where this trial is running
Kristianstad, Skåne County and 1 other locations
- Region Skåne — Kristianstad, Skåne County, Sweden (Recruiting)
- Region Värmland — Karlstad, Värmland County, Sweden (Recruiting)
Study contacts
- Principal investigator: Marie Holmefur, PhD — Örebro University, Sweden
- Study coordinator: Elin Widmark, MSc
- Email: elin.widmark@oru.se
- Phone: +46108319064
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.