Occupational Performance Coaching in Mothers of Children With Cerebral Palsy
May 2, 2017 updated by: mina ahmadi kahjoogh, University of Social Welfare and Rehabilitation Science
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Tehran, Iran, Islamic Republic of, 0098
- Mina Ahmadi Kahjoogh
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years to 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: OT
standard OT
|
|
|
Experimental: OT+OPC
occupational performance coaching
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Canadian Occupational Performance Measure
Time Frame: 10 weeks
|
It is a questionnaire.
|
10 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sherer general self-efficacy
Time Frame: 10 weeks
|
It is a questionnaire.
|
10 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 26, 2016
Primary Completion (Actual)
January 19, 2017
Study Completion (Actual)
January 19, 2017
Study Registration Dates
First Submitted
September 21, 2016
First Submitted That Met QC Criteria
September 26, 2016
First Posted (Estimate)
September 27, 2016
Study Record Updates
Last Update Posted (Actual)
May 5, 2017
Last Update Submitted That Met QC Criteria
May 2, 2017
Last Verified
May 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IR.USWR.REC.1395.148
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.