"Turkish Validity and Reliability of the Temperature Sensitivity Scale for Individuals With Parkinson's Disease"

July 14, 2026 updated by: Nuray Alaca, Acibadem University

Cross-Cultural Adaptation and Psychometric Evaluation of the Turkish Version of the Temperature Sensitivity Scale in Individuals With Parkinson's Disease

The aim of this study is to examine the validity and reliability of the Turkish version of the Temperature Sensitivity Scale in individuals with Parkinson's disease. This cross-sectional methodological study will evaluate the psychometric properties of the scale, including internal consistency, test-retest reliability, and construct validity, in order to provide a valid and reliable tool for assessing temperature sensitivity in Turkish-speaking individuals with Parkinson's disease.

Study Overview

Status

Recruiting

Study Type

Observational

Enrollment (Estimated)

100

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

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

The study population will consist of individuals with clinically diagnosed Parkinson's disease (Hoehn and Yahr stage 1-3), aged between 40 and 85 years, with adequate cognitive function (MMSE ≥ 24). Participants will be recruited from patients attending the Movement Disorders Outpatient Clinic of the Neurology Department. The study population represents ambulatory individuals with mild to moderate disease severity suitable for comprehensive biopsychosocial assessment.

Description

Inclusion Criteria:

  • Clinical diagnosis of Parkinson's disease Hoehn and Yahr stage 1-3 Age between 40 and 85 years Mini-Mental State Examination (MMSE) score ≥ 24 Sufficient cognitive function to communicate and complete assessments Patients attending the Movement Disorders Outpatient Clinic of the Neurology Department Willingness to participate and provide written informed consent

Exclusion Criteria:

  • Presence of psychiatric disorders (e.g., major depression or psychotic disorders) Diagnosis of advanced dementia Presence of uncontrolled systemic chronic diseases (e.g., diabetes mellitus or hypertension) Presence of severe cardiovascular or respiratory conditions Presence of additional orthopedic or neurological conditions that may affect test performance Severe visual or hearing impairments that could interfere with assessments Inability to cooperate adequately with the physiotherapist during assessments

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
Temperature Sensitivity Scale Total Score
Time Frame: Baseline (at the time of questionnaire administration)
Temperature sensitivity will be assessed using the Turkish version of the Temperature Sensitivity Scale in individuals with Parkinson's disease. The scale is designed to evaluate temperature sensitivity-related symptoms and their impact on daily life. Psychometric properties including internal consistency, test-retest reliability, and construct validity will be analyzed. Higher scores indicate greater temperature sensitivity-related problems.
Baseline (at the time of questionnaire administration)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Parkinson's Disease Questionnaire-39 (PDQ-39) Total and Subscale Scores
Time Frame: Baseline (at the time of questionnaire completion)
Quality of life will be assessed using the Parkinson's Disease Questionnaire-39 (PDQ-39), a validated self-report measure specific to Parkinson's disease. The questionnaire consists of 39 items across 8 domains, including mobility, activities of daily living, emotional well-being, stigma, social support, cognition, communication, and bodily discomfort. Scores can be transformed to a 0-100 scale, with higher scores indicating worse quality of life. PDQ-39 scores will be used to evaluate the construct validity of the Turkish version of the Temperature Sensitivity Scale.
Baseline (at the time of questionnaire completion)

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)

May 25, 2026

Primary Completion (Estimated)

December 25, 2026

Study Completion (Estimated)

May 25, 2027

Study Registration Dates

First Submitted

July 14, 2026

First Submitted That Met QC Criteria

July 14, 2026

First Posted (Actual)

July 17, 2026

Study Record Updates

Last Update Posted (Actual)

July 17, 2026

Last Update Submitted That Met QC Criteria

July 14, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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