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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03120858
Other study ID # GO 14/568
Secondary ID
Status Completed
Phase N/A
First received April 16, 2017
Last updated August 10, 2017
Start date January 2015
Est. completion date January 2017

Study information

Verified date August 2017
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 185
Est. completion date January 2017
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Determine what the imagery levels are
Determine the motor imagery: kinesthetic and visual imagery

Locations

Country Name City State
Turkey Istanbul Medipol University Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cronbach's Alpha coefficient 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
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