About this trial
Background and Rationale: The current study is based on the knowledge about the widespread impact of intellectual developmental disabilities (IDD) on the functioning of children and adolescents and the lack of evidence-based intervention programs for this population. There is preliminary research evidence about the effectiveness of cognitive-functional intervention according to the OP-CO approach among children with various cognitive impairments. This study is part of a larger study that aims to adapt the intervention protocol adapted according to the principles of the OP-CO approach for children/adolescents with IDD and will focus on an initial examination of the effectiveness of the intervention according to the adapted protocol. The importance of the study for the topic of intellectual disability: Developing an adapted, applicable and evidence-based protocol can address the unique needs of the population of children/adolescents with IDD (up to age 21) and serve as a tool for occupational therapists who treat this population. The development of the protocol will respond to The lack of evidence-based intervention programs for this population.
Research methodology: A pilot study that will be based on the results of a previous study that includes the development of an adapted intervention protocol.
In this study, an intervention will be delivered for approximately 12-15 weeks once a week for 45 minutes by 3-5 occupational therapists among approximately 10 children/adolescents up to the age of 21 with MSH. The intervention will use standard tools and documentation of the intervention in a therapist diary
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Children and adolescents aged 10-21 years
a primary diagnosis of mild to moderate IDD by The Ministry of Welfare and Social Affairs
enrolled in special education settings and settings with a long school day/stay; - able to communicate verbally in Hebrew and define at least three goal activities with help from parents/educational/therapeutic staff.
Disqualifiers
complex neurological or psychiatric diagnoses (e.g., cerebral palsy)
sensory limitations (e.g., blindness or deafness).
Trial design
Single group
Treatments tested in this trial
The CO-OP approach (Cognitive Orientation to daily Occupational Performance)
Other interventionExploratory study 3-5 Occupational therapists will offer children and adolescents with IDD to participate in an intervention (once a week, 45 minutes for 12-15 weeks - duration of intervention may vary). Standardized tools will be delivered to children/adolescents before and after the intervention
Treatment groups
Trial outcomes
Primary outcomes
anadian Occupational Performance Measure (COPM).
This measure evaluates changes in participants' perceptions of their daily task performance and satisfaction before and after the intervention. Scale Details: Scale Title: COPM Performance and Satisfaction Scales Range: 1 to 10 Interpretation: Higher scores indicate better performance and greater satisfaction. Time Frame: Before and after the intervention (approximately 12-15 weeks).
Locations
Sponsors and contacts
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Miri Tal-Saban
Lead sponsor
Hebrew University of Jerusalem
Sponsor institution
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