Reliability and Validity of the Turkish Version of Caregiver Functional Use Survey (CFUS) (VERSION)

May 26, 2017 updated by: Ramazan Yildiz, Gazi University

Increasing the number of Turkish version of the questionnaire evaluating hand use, adding the scales that evaluate the selective movements of the upper limb to the evaluations will increase the variety of evaluation methods.

The purpose of this study is to evaluate the validity and reliability of the Turkish version of the Caregiver Functional Use Survey (CFUS)

Study Overview

Status

Unknown

Conditions

Detailed Description

CFUS was designed to assess caregivers' perceptions of how much and how well their child used the involved upper extremity.

Children's upper extremity functions will be assessed with a Jebsen Taylor Hand Function Test. Their family will be asked to fill the CFUS.

Compare the relationship between Jebsen-Taylor Hand Function Test and Turkish Version CFUS. Investigate the internal consistency of Turkish-version of CFUS by using Cronbach's alpha coefficient.

Study Type

Observational

Enrollment (Anticipated)

50

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

  • Turkey
      • Ankara, Turkey, 06560
        • Gazi University

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

3 years to 15 years (CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Children with Hemiplegia Cerebral Palsy

Description

Inclusion Criteria:

  • Ages between 3-15 years
  • Diagnosed as Cerebral Palsy (Hemiplegia)
  • Literate in Turkish language and can complete the questionnaire by primer caregiver

Exclusion Criteria:

  • Cannot understand the questionnaire by themselves.
  • Participants had a botulinum toxin injection within the last 6 months
  • Any surgical correction within the last year

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Validity of Caregiver Functional Use Survey (CFUS)
Time Frame: 8 week
Compare the relationship between Jebsen-Taylor Hand Function Test and Turkish Version CFUS
8 week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reliability of CFUS
Time Frame: 8 week
Investigate the internal consistency of Turkish-version of CFUS by using Cronbach's alpha coefficient.
8 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Gazi University

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)

May 2, 2017

Primary Completion (ANTICIPATED)

July 25, 2017

Study Completion (ANTICIPATED)

August 25, 2017

Study Registration Dates

First Submitted

April 21, 2017

First Submitted That Met QC Criteria

April 25, 2017

First Posted (ACTUAL)

April 26, 2017

Study Record Updates

Last Update Posted (ACTUAL)

May 30, 2017

Last Update Submitted That Met QC Criteria

May 26, 2017

Last Verified

May 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • E.150100

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

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