Turkish Version of the Adapted Social Role Participation Questionnaire

May 21, 2025 updated by: Tugba Gokbel, Kocaeli University

Turkish Version of the Adapted Social Role Participation Questionnaire for Ankylosing Spondylitis: A Study on Its Validity and Reliability

Participation, as defined by the International Classification of Functioning, Disability, and Health (ICF), refers to "engagement in a life situation" and is a key component of functional health beyond physical impairments or activity limitations. Social role participation encompasses various aspects of life, including work, family commitments, social interactions, and leisure activities.

Ankylosing Spondylitis (AS), a chronic inflammatory disease affecting the axial skeleton, significantly impacts patients' ability to maintain social roles due to pain, stiffness, and reduced mobility. Existing studies highlight limitations in employment, relationships, education, and leisure activities among AS patients. While various scales assess participation, the Social Role Participation Questionnaire (SRPQ) uniquely emphasizes subjective aspects such as role importance and satisfaction with performance.

Although validated versions of the SRPQ exist in English, Dutch, and Chinese populations, no culturally adapted tool is available for Turkish-speaking AS patients. This study aims to translate the SRPQ into Turkish and evaluate its validity and reliability as a culturally appropriate instrument for assessing social role participation.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The International Classification of Functioning, Disability and Health (ICF) defines participation as "engagement in a life situation" viewing the concept of participation that a functional element beyond body functions and activity limitations. Role participation can be considered in a multifaceted manner. This includes not only participation in a role but but also perceptions of the role's importance, the assessment of limitations or challenges in-role performance, and satisfaction with the individual's ability to fulfill a role according to personal preference. Social role participation encompasses various aspects of an individual's life, including work, family commitments, social interactions, and leisure activities.

Ankylosing Spondylitis (AS), with its chronic, inflammatory, and progressive nature, primarily affects the sacroiliac joints and axial skeleton, leading to pain, joint stiffness, and reduced spinal mobility in individuals. Peripheral and extra-articular symptoms may also occur. Consequently, the physical function loss that develops in individuals reduces their quality of life and productivity, negatively impacting social role participation and the ability to maintain communal roles, affecting their overall well-being. According to the literature, it is documented that individuals with AS experience mild or greater limitations in areas such as recreation and leisure, social life, employment, close relationships, formal and informal social relationships, basic and complex interpersonal interactions, family relationships, education, and contributing to others' well-being.

Existing scales related to participation differ based on the roles they include and the social dimensions they asses (vary based on the different participation roles they include and the dimensions of social roles they measure). Unlike other participation scales that assess social role participation based on frequency, restriction, or role occupation, the SRPQ is a promising tool that emphasizes the assessment of an individual's subjective aspects, particularly their desires and satisfactions, across a wide range of roles in various dimensions. From an individual perspective, the "satisfaction" dimension is particularly noteworthy, as it can be linked to numerous aspects of participation performance and other qualitative dimensions. It provides additional insights into the personal assessment of role performance. Furthermore, the "importance of the role" dimension, which reflects the value an individual assigned to a role, serves as a potential factor that qualifies performance scores. Its direct assessment may offer a possible approach to studying response shift phenomena, which influence many of the subjective aspects of participation.

The English, Dutch, and Chinese versions of the SRPQ have been proven to be reliable and valid tools for measurement assessing social role participation in individuals with AS. Davis et al. have reported that this tool can also be used to evaluate the complex relationships between symptoms, disability, and participation, along with the personal and environmental contextual factors that influence them.

Currently, in Turkey, there is no valid and reliable tool that simultaneously evaluates the importance, physical difficulty, and satisfaction related to social role participation in individuals with AS. This study aims to translate the SRPQ, into Turkish as it encompasses all dimensions of social role participation, and to evaluate its validity and reliability among Turkish-speaking individuals with AS, thereby providing a culturally appropriate assessment tool.

Study Type

Observational

Enrollment (Actual)

129

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
      • Kocaeli, Turkey
        • Kocaeli 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

Primary care clinic

Description

Inclusion Criteria:

  • Clinical diagnosis of AS according to the modified New York criteria
  • Being over 18 years old
  • To comprehend Turkish and communicate fluently in the Turkish language

Exclusion Criteria:

  • Having severe psychiatric conditions
  • Concomitant severe medical conditions

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
Reliability of the Turkish Version of the Adapted Social Role Participation Questionnaire (SRPQ) in Ankylosing Spondylitis
Time Frame: 2018-2022
To assess reliability, the Social Role Participation Questionnaire (SRPQ) was completed twice by the same participants in a quiet room at two-week intervals. Internal consistency was evaluated using Cronbach's alpha (α ≥ 0.70, acceptable), and test-retest reliability was assessed using the Intraclass Correlation Coefficient (ICC ≥ 0.85, excellent), based on a two-way mixed-effects model with absolute agreement. The SRPQ includes three dimensions: Role Importance (1-5), Satisfaction with Performance (1-5), and Physical Difficulty (1-4). Higher scores on Role Importance and Satisfaction indicate better perceived participation, while higher scores on Physical Difficulty reflect greater difficulty in performing roles.
2018-2022
Validity of the Turkish Version of the Adapted Social Role Participation Questionnaire (SRPQ) in Ankylosing Spondylitis
Time Frame: 2018-2022
Construct validity was evaluated by correlating SRPQ scores with three validated instruments: the Ankylosing Spondylitis Quality of Life Scale (ASQoL), Short Form-36 Health Survey (SF-36), and Work Productivity and Activity Impairment Questionnaire (WPAI). ASQoL (0-18) assesses disease-specific quality of life, with higher scores reflecting greater impairment. SF-36 covers eight health domains (0-100), with higher scores indicating better health. Participation was captured in the social functioning, role-physical, and role-emotional domains. The WPAI (0-100%) measures work productivity and activity impairment over the prior week, with higher percentages indicating greater disability. Spearman correlation coefficients were used and interpreted as poor (<0.20), fair (0.21-0.40), moderate (0.41-0.60), very good (0.61-0.80), or excellent (>0.81). The scoring directionality of each scale supports the interpretation of SRPQ's convergent and discriminant validity.
2018-2022

Collaborators and Investigators

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

Sponsor

Kocaeli University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

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)

December 24, 2018

Primary Completion (Actual)

November 29, 2022

Study Completion (Actual)

March 28, 2023

Study Registration Dates

First Submitted

March 12, 2025

First Submitted That Met QC Criteria

April 21, 2025

First Posted (Actual)

April 29, 2025

Study Record Updates

Last Update Posted (Actual)

May 25, 2025

Last Update Submitted That Met QC Criteria

May 21, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 6/56

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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