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Occupational Performance Coaching in Mothers of Children With Cerebral Palsy

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ClinicalTrials.gov Identifier: NCT02915926
Recruitment Status : Completed
First Posted : September 27, 2016
Last Update Posted : May 5, 2017
Sponsor:
Information provided by (Responsible Party):
mina ahmadi kahjoogh, University of Social Welfare and Rehabilitation Science

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.

Condition or disease Intervention/treatment Phase
Cerebral Palsy Behavioral: occupational performance coaching Behavioral: standard OT Not Applicable

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 30 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Actual Study Start Date : July 26, 2016
Actual Primary Completion Date : January 19, 2017
Actual Study Completion Date : January 19, 2017

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Active Comparator: OT
standard OT
Behavioral: standard OT
Experimental: OT+OPC
occupational performance coaching
Behavioral: occupational performance coaching
Behavioral: standard OT



Primary Outcome Measures :
  1. Canadian Occupational Performance Measure [ Time Frame: 10 weeks ]
    It is a questionnaire.


Secondary Outcome Measures :
  1. Sherer general self-efficacy [ Time Frame: 10 weeks ]
    It is a questionnaire.



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Ages Eligible for Study:   25 Years to 50 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
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


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02915926


Locations
Iran, Islamic Republic of
Mina Ahmadi Kahjoogh
Tehran, Iran, Islamic Republic of, 0098
Sponsors and Collaborators
University of Social Welfare and Rehabilitation Science

Responsible Party: mina ahmadi kahjoogh, principal investigator, University of Social Welfare and Rehabilitation Science
ClinicalTrials.gov Identifier: NCT02915926     History of Changes
Other Study ID Numbers: IR.USWR.REC.1395.148
First Posted: September 27, 2016    Key Record Dates
Last Update Posted: May 5, 2017
Last Verified: May 2017

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Cerebral Palsy
Brain Damage, Chronic
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases