- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06356428
Psychometric Properties and Cross-cultural Adaptation of the Turkish Version of Physcian Attitudes Toward Cardiac Rehabilitation and Referral Scale-Revised (PACRR-R)
February 18, 2026 updated by: Haluk Tekerlek, Karamanoğlu Mehmetbey University
Research has reported that the reasons for low implementation of CR are multifactorial at the health system, physician and patient levels.
It has also been found that patients are more likely to initiate CR if physicians strongly and positively promote the importance of CR participation.
Unfortunately, there are insufficient and ineffective data on CR, referral to CR and both clinical and cost-effectiveness outcomes of CR in Turkey.
In this context, it is important to examine more objectively from the perspective of physicians who play a key role in referring patients to CR.
However, in our country, there is no relatively objective measurement tool to evaluate physicians' attitudes towards CR.
Therefore, this study aims to adapt the original "Physician Attitudes towards Cardiac Rehabilitation and Referral Scale-Revised (PACRR-R)" into Turkish and to examine its psychometric properties.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
89
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
-
-
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Karaman, Turkey (Türkiye)
- Karamanoğlu Mehmetbey 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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The population of the study is physicians.
The sample was physicians who volunteered to participate in the study, to whom the study could be announced/notified, and who provided active service in patient diagnosis and treatment.
In the literature, it is stated that the number of individuals to be included in the study in order to achieve meaningful and valid results in the scale development process is at least 5 times the number of items in the scale and ideally 10 times.
In our study, the number of individuals to be included in the study to test the validity of the scale was planned to be at least 100 individuals (PACRR-R consists of 20 items).
In order to examine the test-retest reliability of the scale, it was planned to reapply the scale to at least 25% of the individuals in the sample.
Description
Inclusion Criteria:
- To be a physician,
- Providing active service in patient diagnosis and treatment
Exclusion Criteria:
- Not providing active service in patient diagnosis and treatment despite being a physician (administrative position, etc.).
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 |
|---|---|---|
|
Physician Attitudes toward Cardiac Rehabilitation and Referral (PACRR)-Revised Scale Score
Time Frame: 10-15 minutes
|
The Physician Attitudes toward Cardiac Rehabilitation and Referral (PACRR)-Revised Scale comprises 20 items to assess physicians' attitudes and beliefs about CR and referral.
Response options were 1 = strongly disagree, 2 = agree, 3 = neutral, 4 = agree, and 5 = strongly agree.
Five (5) items are reverse-scored to mitigate acquiescence bias (denoted with *), such that higher scores reflect more positive attitudes toward CR and referral.
A mean score is computed for the total (where at least 80% of items were completed; i.e., 15/19) scale and subscales.
A final open-ended item asks physicians to list the most important factors that influence their decision to refer a patient to CR.
|
10-15 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 13, 2024
Primary Completion (Actual)
May 30, 2025
Study Completion (Actual)
January 15, 2026
Study Registration Dates
First Submitted
April 4, 2024
First Submitted That Met QC Criteria
April 4, 2024
First Posted (Actual)
April 10, 2024
Study Record Updates
Last Update Posted (Actual)
February 20, 2026
Last Update Submitted That Met QC Criteria
February 18, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- KARYÖN-DR
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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