Psychological Readiness of Injured Athlete to Return to Sport (PRIA-RS)

October 1, 2024 updated by: Gürkan Demirtas, Nigde Omer Halisdemir University

Turkish Adaptation, Validity and Reliability of the Psychological Readiness of Injured Athlete to Return to Sport (PRIA-RS) Questionnaire

Clinicians are recommended to assess athletes during the rehabilitation phase to identify athletes with potentially maladaptive psychological responses to injury. Therefore, the Psychological Readiness of Injured Athlete to Return to Sport (PRIA-RS) questionnaire was developed to assess the athlete's psychological readiness to return to sport. The aim of this study was to adapt the PRIA-RS questionnaire into Turkish and to establish its validity and reliability. Serial approach method will be used while translating the questionnaire into Turkish. In order to evaluate the validity of PRIA-RS, The Re-injury Anxiety Inventory and Tampa Kinesiophobia Scale will be applied to the participants.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

100

Phase

  • Not Applicable

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

  • Turkey
    • Çankaya
      • Ankara, Çankaya, Turkey, 06490
        • Gazi 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

Description

Inclusion Criteria:

  • athletes who have missed at least 2 months of training due to injury
  • having an upper, lower extremity or spine injury

Exclusion Criteria:

  • having a psychological disorder
  • regular use of psychiatric medication

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

  • Primary Purpose: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Patient group
athletes who have suffered a sports injury
Diagnostic test: Turkish adaptation, validity and reliability
This study was conducted as "test-retest" design and the psychometric properties of PRIA-RS were examined in injured athletes

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Psychological Readiness of Injured Athlete to Return to Sport (PRIA-RS)
Time Frame: Baseline
The PRIA-RS questionnaire provides a comprehensive screening of psychological readiness for return to sport based on athlete-reported confidence, self-perception, insecurity and fear of re-injury at the end of competition. The PRIA-RS questionnaire consists of 10 questions with each question scored on a 5-point Likert scale (50 points total), with a higher score representing a more positive psychological response.
Baseline
Re-injury Anxiety Inventory (RAI):
Time Frame: Baseline
The questionnaire developed by Walker et al. to measure re-injury anxiety is a 4-point Likert-type questionnaire and consists of 28 items in total. The questionnaire consists of two subgroups including re-injury anxiety/concern about rehabilitation and re-injury anxiety/concern about return to sport and training. A higher score represents more re-injury anxiety.
Baseline
Tampa kinesiophobia scale (TKS)
Time Frame: Baseline
It is a 17-question scale developed to measure fear of movement/reinjury. The scale includes parameters of injury/re-injury and fear-avoidance in work-related activities. The scale uses a 4-point Likert scale (Strongly disagree=1, Strongly agree=4). A higher score represents more kinesiophobia.
Baseline

Collaborators and Investigators

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

Sponsor

Nigde Omer Halisdemir University

Collaborators

Gazi 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)

February 1, 2023

Primary Completion (Actual)

June 1, 2024

Study Completion (Actual)

June 1, 2024

Study Registration Dates

First Submitted

July 22, 2023

First Submitted That Met QC Criteria

July 22, 2023

First Posted (Actual)

August 1, 2023

Study Record Updates

Last Update Posted (Actual)

October 3, 2024

Last Update Submitted That Met QC Criteria

October 1, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 16.12.2022

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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