Turkish Version of Mini-BESTest, Validity and Reliability for Adult Participants With Sensoriomotor Impairments
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|ClinicalTrials.gov Identifier: NCT03839381|
Recruitment Status : Not yet recruiting
First Posted : February 15, 2019
Last Update Posted : February 15, 2019
|Condition or disease|
|Parkinson Disease Multiple Sclerosis Trauma, Brain|
Physical therapists encounter postural control problems frequently. These problems require multifaceted assessment. Therefore, the treatment of postural control problems should be planned after a multifaceted assessment.
Balance Evaluation Systems Test (BESTest) comprises 27 items and evaluate all components of postural control. MiniBESTest is a shortened version of BESTest with 14 tasks. MiniBESTest still addresses almost all components of postural control and can be performed 15 min. MiniBESTest is one of the most common methods which practiced on adult patients.
The aim of this study is to present the Turkish version of miniBESTest which evaluates the reasons of balance deficit and postural control. Accordingly, a practice of validity and reliability on adult participants with sensoriomotor impairments will be performed by utilizing the Turkish version of miniBESTest in this study.
|Study Type :||Observational|
|Estimated Enrollment :||50 participants|
|Official Title:||Turkish Version of Mini-BESTest- Balance Evaluation Systems Test: A Translation and Transcultural Adaptation Study Incorporating Validity and Reliability Analysis for Adult Participants With Sensoriomotor Impairments|
|Estimated Study Start Date :||March 4, 2019|
|Estimated Primary Completion Date :||November 29, 2019|
|Estimated Study Completion Date :||December 4, 2019|
- Mini BESTest [ Time Frame: 10-15 minutes. ]Mini-BESTest focuses on dynamic balance. It includes a total of 14 different tasks, each rated on a 3-level between 0 (severe postural control impairment) and 2 (no postural control impairment) with a maximal score of 28.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03839381
|Contact: Sema Büğüşan Oruç, M.Sc.||+email@example.com|
|Contact: Sevim Acaröz Candan, PhDfirstname.lastname@example.org|