Turkish Version of Back Pain Knowledge and Beliefs Survey (BacKS-tr)

August 14, 2025 updated by: FUAT YUKSEL, T.C. ORDU ÜNİVERSİTESİ

Validity, Reliability, and Cross-Cultural Adaptation of the Turkish Version of Back Pain Knowledge and Beliefs Survey (BacKS)

Low back pain (LBP) is a globally prevalent health issue, affecting the majority of individuals at some point in their lives. Misconceptions about LBP can prolong its chronicity, highlighting the importance of educating patients with accurate information. The Back Pain Knowledge and Beliefs Survey (BacKS), introduced in 2024, aims to measure individuals' knowledge about LBP based on updated scientific evidence. Given the high prevalence of LBP in Turkey and the lack of validated tools in Turkish, adapting BacKS to Turkish is essential. This study aims to conduct its cross-cultural adaptation, validation, and reliability analysis for clinical and community use.

Study Overview

Detailed Description

Low back pain (LBP) is one of the most prevalent health issues worldwide, with approximately three-quarters of individuals experiencing this condition at some point in their lives. Misconceptions, beliefs, and misinformation about LBP can prolong the duration of pain and contribute to its chronicity. Clinical guidelines emphasize the importance of educating patients with evidence-based information to remove potential barriers to recovery.

The Back Pain Knowledge and Beliefs Survey (BacKS) was introduced in October 2024 to assess individuals' knowledge and beliefs about LBP based on the most recent scientific evidence. Several tools in the literature aim to measure knowledge and beliefs related to LBP, including the Back Beliefs Questionnaire (BBQ) and the Back Pain Knowledge Questionnaire. However, these tools were developed in previous decades and may not reflect the current scientific literature. Additionally, the Turkish versions of some of these questionnaires have not yet undergone validation and reliability studies.

According to the 2016-2022 Turkish Health Survey conducted by the Turkish Statistical Institute (TÜİK), back-related problems rank first among all reported health issues, with a prevalence rate of 24.6%. Despite the high prevalence of LBP in Turkey, there is currently no systematically validated tool available in Turkish to measure the public's knowledge and beliefs regarding this condition.

The adaptation of BacKS into Turkish will help address this gap by providing a valid and reliable tool for both clinical and community-based research. Measuring and evaluating patient-reported outcomes accurately is crucial in managing LBP effectively. Therefore, the aim of this study is to conduct the cross-cultural adaptation, validation, and reliability analysis of the Turkish version of BacKS.

Study Type

Observational

Enrollment (Estimated)

200

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

    • Altinordu
      • Ordu, Altinordu, Turkey, 52200
        • Ordu 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

Yes

Sampling Method

Probability Sample

Study Population

Individuals with current low back pain or a history of low back pain in the last 12 months.

Description

Inclusion Criteria:

  • Having low back pain or having a history of low back pain in the last 12 months
  • To be able to read and write Turkish

Exclusion Criteria:

  • Having cognitive impairment that prevents communication
  • Pregnancy
  • Malignite
  • Infections
  • Fractures,
  • Inflammatory diseases

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
Test-retest group
One hundred of the participants who were administered the Tr-BacKS will fill out the same form again after 1 week.
100 people will fill in the Backs-tr again after 1 week.
Test group
The questionnaire will be administered once to these 100 participants
200 people will be administered The Back Belief Questionnaire Tr (BBQ) and Backs-tr.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Validation
Time Frame: 15.01.2025- 15.04.2025
200 people will be compared with the scores obtained from the Backs-Tr questionnaire
15.01.2025- 15.04.2025
The Back Belief Questionnaire (BBQ).
Time Frame: 15.01.2025- 15.04.2025
200 people will be compared with the scores obtained from The Back Belief Questionnaire (BBQ).
15.01.2025- 15.04.2025

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reliability
Time Frame: 15.01.2025- 15.04.2025
One hundred of the participants who were administered the Tr-BacKS will fill out the same form again after 1 week. The two measurement scores obtained from the participants will be compared using the Intraclass Correlation Coefficient (ICC).
15.01.2025- 15.04.2025
Internal Consistency Reliability
Time Frame: 15.01.2025- 15.04.2025
Internal consistency will be assessed separately for the biomedical (9 items) and self-care factor (11 items) in the original questionnaire. Internal consistency reliability will also be assessed for all items. Cronbach's Alpha will be used in the evaluation.
15.01.2025- 15.04.2025

Collaborators and Investigators

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

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)

November 15, 2024

Primary Completion (Estimated)

November 15, 2025

Study Completion (Estimated)

December 15, 2025

Study Registration Dates

First Submitted

January 6, 2025

First Submitted That Met QC Criteria

January 16, 2025

First Posted (Actual)

January 17, 2025

Study Record Updates

Last Update Posted (Estimated)

August 15, 2025

Last Update Submitted That Met QC Criteria

August 14, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • E-14647249-000-1075264

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

product manufactured in and exported from the U.S.

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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