Turkish Version of the Kinesthetic and Visual Imagery Questionnaire

August 10, 2017 updated by: Burcu Dilek, Hacettepe University

Reliability and Validity of the Turkish Version of the Kinesthetic and Visual Imagery Questionnaire

Imagery is determined with two strategies to mentally simulate the movements: visual and kinesthetic imagery. Visual motor imagery (VMI) is associated with spatial coordinates of a movement in the environment and through this speciality VMI applies mainly to the imagery of moving objects or to movement of another person in the imagined environment, although imagine of own movement is also possible. Kinesthetic motor imagery depends on dynamic relationship among the individual, the movement and the environment and it should be determined by the nature of the task, the environment and individual characteristics and also requires "feel" the movement.

The aim of this study is to translate this questionnaire into Turkish and the translation in terms of its internal consistency, test-retest reliability.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

185

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

      • Istanbul, Turkey
        • İstanbul Medipol 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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Healthy volunteers

Description

Inclusion Criteria:

  • ages between 18-65 years, healthy volunteers, with no limitation in mobility or movement disorder, with no chronic pain

Exclusion Criteria:

  • refuse to attend to the study, neurological conditions

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
Cronbach's Alpha coefficient
Time Frame: 2 years
Cronbach's Alpha coefficient was used to determine internal consistency of the questionnaire and its subscales. Cronbach's Alpha Coefficient greater than 0.8 is generally considered acceptable.
2 years

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)

January 1, 2015

Primary Completion (Actual)

May 1, 2016

Study Completion (Actual)

January 1, 2017

Study Registration Dates

First Submitted

April 16, 2017

First Submitted That Met QC Criteria

April 16, 2017

First Posted (Actual)

April 19, 2017

Study Record Updates

Last Update Posted (Actual)

August 14, 2017

Last Update Submitted That Met QC Criteria

August 10, 2017

Last Verified

August 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • GO 14/568

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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