Turkish Version of the Kinesthetic and Visual Imagery Questionnaire

• Sponsor: Hacettepe University (Other)
• Overall Status: Completed
• CT.gov ID: NCT03120858
• Collaborator: (none)
• Enrollment: 185
• Location: 1
• Actual Duration (Months): 24
• Patients Per Site Per Month: 7.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Image, Body; Healthy; Pain	Behavioral: Determine what the imagery levels are

Study Design

• Study Type: Observational
• Actual Enrollment: 185 participants
• Observational Model: Other
• Time Perspective: Prospective
• Official Title: Reliability and Validity of the Turkish Version of the Kinesthetic and Visual Imagery Questionnaire
• Actual Study Start Date: Jan 1, 2015
• Actual Primary Completion Date: May 1, 2016
• Actual Study Completion Date: Jan 1, 2017

Outcome Measures

Primary Outcome Measures

1. Cronbach's Alpha coefficient [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.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 65 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Istanbul Medipol University	Istanbul		Turkey

Sponsors and Collaborators

• Hacettepe University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Burcu Dilek, PT, MS, PhD, Assist Prof, Hacettepe University
• ClinicalTrials.gov Identifier: NCT03120858
• Other Study ID Numbers: GO 14/568
• First Posted: Apr 19, 2017
• Last Update Posted: Aug 14, 2017
• Last Verified: Aug 1, 2017

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Burcu Dilek, PT, MS, PhD, Assist Prof, Hacettepe University: motor imagery; kinesthetic imagery; reliability; Turkish version

Study Results

No Results Posted as of Aug 14, 2017