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Occupational Performance Coaching in Mothers of Children With Cerebral Palsy

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
mina ahmadi kahjoogh, University of Social Welfare and Rehabilitation Science
ClinicalTrials.gov Identifier:
NCT02915926
First received: September 21, 2016
Last updated: May 2, 2017
Last verified: May 2017
  Purpose
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 Intervention
Cerebral Palsy Behavioral: occupational performance coaching Behavioral: standard OT

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment

Resource links provided by NLM:


Further study details as provided by mina ahmadi kahjoogh, University of Social Welfare and Rehabilitation Science:

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


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


Enrollment: 30
Actual Study Start Date: July 26, 2016
Study Completion Date: January 19, 2017
Primary Completion Date: January 19, 2017 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: OT
standard OT
Behavioral: standard OT
Experimental: OT+OPC
occupational performance coaching
Behavioral: occupational performance coaching Behavioral: standard OT

  Eligibility

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

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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
  More Information

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
Study First Received: September 21, 2016
Last Updated: May 2, 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

ClinicalTrials.gov processed this record on August 18, 2017