Occupational Performance Coaching in Mothers of Children With Cerebral Palsy
Primary Purpose
Cerebral Palsy
Status
Completed
Phase
Not Applicable
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
occupational performance coaching
standard OT
Sponsored by
About this trial
This is an interventional treatment trial for Cerebral Palsy
Eligibility Criteria
Inclusion Criteria:
mothers: being literate 25 to 25 caring nobody disabled other than her child children: 5 to 12 cerebral palsy
Exclusion Criteria:
children: others problems that affect on communication
Sites / Locations
- Mina Ahmadi Kahjoogh
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
OT
OT+OPC
Arm Description
standard OT
occupational performance coaching
Outcomes
Primary Outcome Measures
Canadian Occupational Performance Measure
It is a questionnaire.
Secondary Outcome Measures
Sherer general self-efficacy
It is a questionnaire.
Full Information
NCT ID
NCT02915926
First Posted
September 21, 2016
Last Updated
May 2, 2017
Sponsor
University of Social Welfare and Rehabilitation Science
1. Study Identification
Unique Protocol Identification Number
NCT02915926
Brief Title
Occupational Performance Coaching in Mothers of Children With Cerebral Palsy
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
July 26, 2016 (Actual)
Primary Completion Date
January 19, 2017 (Actual)
Study Completion Date
January 19, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Social Welfare and Rehabilitation Science
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
A single-blind Randomized Controlled Trial will be used to test the efficacy of the OPC on self-efficacy and occupational performance with mothers of children with cerebral palsy. Canadian Occupational Performance Measurement and Sherer general self-efficacy scale will be employed to data collection. The sample size was determined for each group of 15 people. The participants conveniently and according to inclusion and exclusion criteria will be randomized into the groups. Participants in the intervention group will be participated in 10 sessions of OPC. At the end the questionnaires will be completed by both groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
OT
Arm Type
Active Comparator
Arm Description
standard OT
Arm Title
OT+OPC
Arm Type
Experimental
Arm Description
occupational performance coaching
Intervention Type
Behavioral
Intervention Name(s)
occupational performance coaching
Intervention Type
Behavioral
Intervention Name(s)
standard OT
Primary Outcome Measure Information:
Title
Canadian Occupational Performance Measure
Description
It is a questionnaire.
Time Frame
10 weeks
Secondary Outcome Measure Information:
Title
Sherer general self-efficacy
Description
It is a questionnaire.
Time Frame
10 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
mothers: being literate 25 to 25 caring nobody disabled other than her child children: 5 to 12 cerebral palsy
Exclusion Criteria:
children: others problems that affect on communication
Facility Information:
Facility Name
Mina Ahmadi Kahjoogh
City
Tehran
ZIP/Postal Code
0098
Country
Iran, Islamic Republic of
12. IPD Sharing Statement
Learn more about this trial
Occupational Performance Coaching in Mothers of Children With Cerebral Palsy
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