- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05405036
The Psychometric Properties of the Turkish Version of Interpersonal Communication Questionnaire
The Psychometric Properties of the Turkish Version of Interpersonal Communication Questionnaire in Physiotherapy Students
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Istanbul, Turkey, +90
- Acıbadem University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Students taking the Measurement and Evaluation II course in Physiotherapy and Rehabilitation
Exclusion Criteria:
- Not volunteering
- Those who are being treated with any psychiatric diagnosis
- Students who fail the course or fail to pass it successfully
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Students
60 second-year students studying at the Department of Physiotherapy and Rehabilitation at University are planned to attend.
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In the last month of the Measurement and Evaluation course in Physiotherapy, a simulated patient session will be held four times (with disease in the cervical-lumbar-shoulder and knee region).
Students will be evaluated by the methods they learned about patients.
10 days before and after the simulated patient sessions, the questionnaire will be applied in Turkish for validity and reliability, and then the questionnaire will be repeated after the simulated patient sessions are over, and the effect of the smile patient sessions on the perceived communication skills of the patient will be examined.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Interpersonal Communication Questionnaire
Time Frame: Change from Baseline Scores at 2 week and 6. week
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Eight statements were constructed; four related to a sub-scale measuring factors associated with communication anxiety, and four related to communication confidence. Each statement had a 5-point Likert scale ranging from 1 = strongly disagree to 5 = strongly agree. Sub-scale scores ranged from a possible 4-20; a higher score indicating either higher levels of communication confidence or anxiety. |
Change from Baseline Scores at 2 week and 6. week
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Visual Analog Scale
Time Frame: Change from Baseline Scores at 6. week
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A visual analog scale between 0 and 10 will be used to evaluate communication anxiety, stress, motivation and success that may occur when students go into clinical practice at the beginning and end of the term and when they meet with the patient.Zero will be determined to be none at all, and 10 to the maximum I can think of
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Change from Baseline Scores at 6. week
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Interpersonal Communication Competence Inventory
Time Frame: Change from Baseline Scores at 6. week
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Huang and Lin (18) developed the CITI based on four basic skill areas (listening skill, empathy skill, expression skill, social relaxation skill) in order to evaluate the communication competence of university students in accordance with the relational approach.The scores that can be obtained from the measurement tool vary between 15 and 75.
Items 10 and 13 are reverse scored.
A high score on the measurement tool indicates a high level of interpersonal communication competence.
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Change from Baseline Scores at 6. week
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nuray ALACA, Acibadem University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- ATADEK-2022/08/01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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