Investigating Best Practices for Children With Cerebral Palsy: A Pilot Study of Two Approaches
1 other identifier
interventional
18
0 countries
N/A
Brief Summary
This project (CO-OP II) is the second in a series of three studies to validate a new treatment approach for children with cerebral palsy (CP). The initial study was comprised of a series of four single case studies with children with CP. It evaluated the potential of the Cognitive Orientation to Occupational Performance (CO-OP) approach to be used with children with CP and tested the procedures for CO-OP II. The overall objective of the full series of studies is to determine whether better functional outcomes are achieved for children with CP with CO-OP intervention than with contemporary occupational therapy treatment. The primary objective of CO-OP II is to establish the feasibility of conducting a full scale randomize control trial (RCT) to discover if there are differences in functional outcomes (i.e., improvement in task performance, self efficacy) between a group of children with CP receiving CO-OP therapy and a group receiving a contemporary treatment approach (CTA). In order to meet this objective, a pilot RCT will be conducted to answer the specific research questions outlined below:
- 1.Do children wiht CP acquire the skills they set as goals in each of the two treatment groups?
- 2.Do the acquired skills generalize and transfer?
- 3.Are the skills maintained at 4 months post intervention?
- 4.Does the CO-OP approach produce a larger effect on skill acquisition and self efficacy than the CTA?
- 5.Does amount of parent involvement have any effect on skill acquisition or self efficacy?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Dec 2006
Typical duration for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2006
CompletedFirst Submitted
Initial submission to the registry
January 30, 2007
CompletedFirst Posted
Study publicly available on registry
February 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2009
CompletedAugust 13, 2009
August 1, 2009
January 30, 2007
August 12, 2009
Conditions
Interventions
Eligibility Criteria
You may qualify if:
- between 7 and 12 years of age
- diagnosis of cerebral palsy with hemiplegia or spastic diplegia
- Level 1,2 or 3 on the Gross Motor Function Classification Scale(GMFCS)
- normal intelligence (IQ\> 85 on at least one scale (verbal or performance) of the Kaufman Brief Intelligence Test (KBIT-2)
- child assent and agreement to participate
- parental consent and agreement to participate
- sufficient language ability to communicate with and be understood during treatment
You may not qualify if:
- previously received or presently receiving a cognitive treatment for motor-based performance problems
- use of alternative communication system such as PECS or communication board
- regular use of BOTOX during intervention period
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Torontolead
- Holland Bloorview Kids Rehabilitation Hospitalcollaborator
- ErinoakKidscollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Debra L Cameron, PhD. O.T.
University of Toronto
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
January 30, 2007
First Posted
February 1, 2007
Study Start
December 1, 2006
Study Completion
September 1, 2009
Last Updated
August 13, 2009
Record last verified: 2009-08