Turkish Validity and Reliability of The Tampa Scale for Kinesiophobia for Temporomandibular Disorders

NCT ID: NCT04644263

Last Updated: 2020-11-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

111 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-11-01

Study Completion Date

2017-08-02

Brief Summary

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Objective: The aim of this study is to evaluate the validity and reliability of the Turkish version of the 'The Tampa Scale for Kinesiophobia for Temporomandibular Disorders (TSK-TMD)' questionnaire used to assess kinesiophobia in temporomandibular joint disorders.

Method: The "Tampa Kinesiophobia Scale in Temporomandibular Disorders" (TSK-TMD), which consists of 12 item, was adapted to Turkish with the translation and back-translation method. 111 patients (75 females, 36 males) who had been diagnosed with temporomandibular joint for at least 6 months and diagnosed as Temporomandibular Joint Disorder were participated to fill out the questionnaire. In the present study, participants were assessed with the Temporomandibular joint disorders evaluation form, Turkish TSK-TMD-12 item, Visuel Analogue Scale (VAS) and Pain Catastrophizing Scale (PCS). The internal consistency and test-retest reliability with a 3-5 days time were used to evaluate the reliability of the TSK-TMD. The reliability of the corelatıon was checked with PCS. Construct validity was assessed based on confirmatory factor analysis (CFA).

Detailed Description

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We used Turkish TSK-TMD-12 item, Visuel Analogue Scale (VAS) and Pain Catastrophizing Scale (PCS) questionnaires in our study.

Conditions

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Temporomandibular Joint Disorders

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Validity and reliability

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* volunteer participation in the study, between 18 and 65 years old,
* having symptoms for at least 6 months,
* being literate, and having communication to understand and answer questions.

Exclusion Criteria

* toothache
* Cognitive impairment affecting their ability to understand and complete the study questionnaire
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Okan University

OTHER

Sponsor Role lead

Responsible Party

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Eylem KÜÇÜK

Head of Physiotherapy

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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Eylem Kucuk, OkanU

Identifier Type: -

Identifier Source: org_study_id