The Psychometric Properties of the Turkish Version of Interpersonal Communication Questionnaire

July 19, 2022 updated by: Nuray Alaca, Acibadem University

The Psychometric Properties of the Turkish Version of Interpersonal Communication Questionnaire in Physiotherapy Students

In a study conducted by Lewis et al. in 2008, an "interpersonal communication" questionnaire was developed to measure the perceived interpersonal skills of physiotherapy and rehabilitation students regarding patient interaction. It was determined that the questionnaire used especially after the simulated patient training increased the communication of physiotherapy and rehabilitation students after the simulated patient training. However, the questionnaire was not translated into Turkish and its validity and reliability were not investigated. Therefore, in this study, the authors aim to investigate the Turkish validity and reliability of the Interpersonal Communication Questionnaire as the primary purpose. Secondly, to investigate the effect of simulated patient experience on the perceived interpersonal skills of physiotherapy and rehabilitation students regarding patient interaction at the time of the clinical trial.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

60

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

      • Istanbul, Turkey, +90
        • Acıbadem University

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

18 years to 25 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

60 second year students aged 18-23 studying at the physiotherapy and rehabilitation department of Acibadem mehmet ali aydınlar university are planned to participate in the research.

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

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Students
60 second-year students studying at the Department of Physiotherapy and Rehabilitation at University are planned to attend.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Interpersonal Communication Questionnaire
Time Frame: Change from Baseline Scores at 2 week and 6. week

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

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Visual Analog Scale
Time Frame: Change from Baseline Scores at 6. week
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
Change from Baseline Scores at 6. week
Interpersonal Communication Competence Inventory
Time Frame: Change from Baseline Scores at 6. week
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.
Change from Baseline Scores at 6. week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nuray ALACA, Acibadem University

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 15, 2022

Primary Completion (Actual)

June 1, 2022

Study Completion (Actual)

June 30, 2022

Study Registration Dates

First Submitted

May 30, 2022

First Submitted That Met QC Criteria

June 2, 2022

First Posted (Actual)

June 3, 2022

Study Record Updates

Last Update Posted (Actual)

July 20, 2022

Last Update Submitted That Met QC Criteria

July 19, 2022

Last Verified

July 1, 2022

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)?

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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