- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01876888
Turkish Cultural Adaptation, Validation and Reliability Study of MedRisk Instrument
Turkish Version of MedRisk Instrument for Measuring Patient Satisfaction With Physical Therapy Care: Its Cultural Adaptation, Validation and Reliability Study
Study Overview
Status
Conditions
Detailed Description
Patient satisfaction with physical therapy has become an important concern in health care, used to monitor patient perceptions of the quality of physical therapy care services. Measurement of patient satisfaction may provide useful information which may improve the quality of health care. The "MedRisk Instrument for Measuring Patient Satisfaction With Physical Therapy Care" (MRPS) is one of these instruments, which has undergone reliability and validation testing.The MRPS is a 20-item (18 items and 2 global measures) questionnaire which assess patient experience about therapist, registration process and convenience of environment.
A survey on a consecutive sample of patients from various regions in Turkey who were receiving outpatient physiotherapy programs was recruited.The study was divided into two phases: Phase I, the cross-cultural adaptation, which involves the translation procedures into Turkish and preliminary probe in the target population; and phase II, which involves the reliability and validation study.
After providing informed consent, for test-retest reliability, all subjects were asked to complete the MRPS twice; the first at least after receiving three sessions of physiotherapy and the second four days later which could coincide with the date of their discharge but not later. Subjects provided information regarding their age, sex, and location of primary symptoms prior to completing the instrument.Factor structure.
The construct validity was evaluated by factor analysis method. An exploratory factor analysis, using principal components analysis with varimax rotation was performed.Criterion validity was addressed by determining the correlation between two global measures of satisfaction and each of the 18 items. The measurement properties of the potential factors were investigated by determining correlations of the factors to the global measures and 10-cm Visual Analog Scale (VAS) which evaluates the level of patient satisfaction with higher scores indicating better satisfaction. Pearson correlation coefficient was used to assess the strength of the linear relationships. Test-retest reliability was examined by calculating the Intraclass Correlation Coefficient (ICC). Internal consistency relates to homogeneity of an instrument, which is assessed with Cronbach's alpha
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All subjects had to be able to read and write in Turkish.
Exclusion Criteria:
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
patient satisfaction instrument
Time Frame: 5 minutes
|
5 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Özgen Aras, T.C. Dumlupınar Üniversitesi
- Principal Investigator: Cigdem Ayhan, Hacettepe University
- Study Chair: Yavuz Yakut, Hacettepe University
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Physiotherapy & Rehabilitation
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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