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Evaluation of CO-OP for Adolescents With Mild Intellectual Disability

Evaluation of The Cognitive Orientation to Daily Occupational Performance (CO-OP) Approach for Adolescents With Mild Intellectual Disability

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06691698
Acronym
CO-OPIF
Enrollment
60
Registered
2024-11-15
Start date
2025-01-16
Completion date
2027-03-31
Last updated
2025-08-29

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

Conditions

Intellectual Disability, Mild

Keywords

adolescents, executive function, metacognition, mild intellectual disability, occupational therapy, occupational performance, person-centered intervention, self-efficacy

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.

Interventions

OTHERThe Cognitive Orientation to Daily Occupational Performance Approach

CO-OP is a client-centred, performance-based, problem-solving focused, occupation-focused and occupation-based intervention. In CO-OP the person is guided to use a meta-cognitive strategy to find his or her own strategies for specific activities. The main purpose is to enable meta-cognitive thinking in every day activities, leading to enhanced self-efficacy, occupational performance and independency.

Sponsors

Landstinget i Värmland
CollaboratorOTHER
Göteborg University
CollaboratorOTHER
Stiftelsen Sunnerdahls Handikappfond
CollaboratorOTHER
Stiftelsen Sävstaholm
CollaboratorUNKNOWN
Majblommans riksförbund
CollaboratorUNKNOWN
Örebro University, Sweden
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

One of the outcomes will be assessed using video from baseline, post and 6 months post intervention, and the assessor of those videos will be blinded to the order and have no knowledge about the participant.

Eligibility

Sex/Gender
ALL
Age
13 Years to 17 Years
Healthy volunteers
No

Inclusion 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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Performance Quality Rating Scale - occupational performance qualityBaseline, up to 4 weeks post intervention and 6 months post interventionObserved performance quality during performing four chosen goal activities thas is filmed and rated 1-10.
Change in Canadian Occupational Performance Measure - performanceBaseline, up to 4 weeks post intervention and 6 months post interventionSelf-rated occupational performance in four chosen goal activities, rated 1-10
Change in Canadian Occupational Performance Measure - satisfactionBaseline, up to 4 weeks post intervention and 6 months post interventionSelf-rated satisfaction with performance in four chosen goal activities, rated 1-10

Secondary

MeasureTime frameDescription
Experiences of CO-OP as a patient - qualitativeUp to 4 weeks post intervention and 6 months post interventionQualitative semi-structured interviews analyzed using qualitative content analysis.
Change in General Self-Efficacy Scale - self-efficacyBaseline, up to 4 weeks post intervention and 6 months post interventionSelf-rated self-efficacy, 10 statements rated 1-4.
Perceptions of CO-OP as a parent of a patient - qualitativeUp to 4 weeks post intervention and 6 months post interventionQualitative semi-structured interviews analyzed using phenomenographic analysis

Other

MeasureTime frameDescription
Feasibility: AcceptabilityUp to 4 weeks post intervention and 6 months post interventionAcceptability will be evaluated by structured interviews. The interview consists of five yes/no questions and a 10 point scale on how much effort the CO-OP intervention required. Data will be on nominal and ordinal level.
Feasibility: AdaptationUp to 1 year after intervention.Whether the CO-OP approach needs any adaptations in order to be feasible for adolescents with mild intellectual disability will be evaluated. This will be done by collecting field notes written by CO-OP therapists and a text analysis with descriptive comparison between notes and the CO-OP manual.
Feasibility: Possible expansion to a new group2024-2025Qualitative text analysis in which contents of the CO-OP manual will be compared with norms and values in the national policy documents for children and youth habilitation. This is carried out to evaluate whether it would be possible to expand this intervention to a new group of patients (adolescents with mild intellectual disability). The data collection is not related to the individual participants.

Countries

Sweden

Contacts

Primary ContactElin Widmark, MSc
elin.widmark@oru.se+46108319064
Backup ContactMarie Holmefur, PhD
marie.holmefur@oru.se+4619303612

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026