Which back pain scale best tracks recovery? a turkish study puts three to the test

NCT ID NCT06271460

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
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Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time

Summary

Researchers are comparing three Turkish questionnaires that measure disability from chronic low back pain: the Roland-Morris Disability Questionnaire, the Oswestry Disability Index, and the Quebec Back Pain Disability Scale. About 80 adults with chronic non-specific low back pain will fill out these questionnaires before and after a four-week physiotherapy program. The goal is to see which questionnaire is most sensitive to real changes in function and to define what counts as a meaningful improvement. This could help clinicians choose the best tool to track progress in Turkish-speaking patients.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Standardized physiotherapy program
What this could lead to
If one questionnaire proves more responsive, clinicians could use it to better measure real-world improvement in Turkish-speaking patients with chronic back pain.
What could go wrong
This is a small observational study, not a treatment trial. Results may not apply to other languages or settings, and the questionnaires may not capture all meaningful changes.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

80 people

The number who actually took part.

Started

Apr 2024

Finished

Jun 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adults aged 18-65 years with chronic non-specific low back pain of at least 12 weeks' duration were consecutively recruited from patients referred for physiotherapy in the outpatient Department of Physical Medicine and Rehabilitation of a tertiary-care hospital in Istanbul, Türkiye. Chronic non-specific low back pain was defined as low back pain not attributable to a specific spinal pathology such as fracture, tumor, infection, inflammatory disease, or radiculopathy.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults aged 18-65 years * Chronic non-specific low back pain of at least 12 weeks' duration * Low back pain not attributable to a specific spinal pathology * Ability to read and understand Turkish * Referral for physiotherapy * Provision of written informed consent Exclusion Criteria: * Previous lumbar spine surgery * Specific spinal pathology or progressive neurological deficits * Systemic inflammatory or neurological disease * Myocardial infarction or cerebrovascular event within the previous 12 weeks * Cognitive impairment (Mini-Mental State Examination score \<24) * Pregnancy * Recent intramuscular analgesic injection * Participation in structured exercise therapy during the previous 6 months

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Acıbadem Health Group

    Istanbul, None Selected, 34752, Turkey (Türkiye)

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