Reformer Pilates vs Conventional Physiotherapy in Chronic Low Back Pain
CompletedNot applicableNCT07543952
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Non-specific chronic low back pain is one of the most prevalent musculoskeletal disorders worldwide and is associated with functional limitations and reduced quality of life. Exercise-based physiotherapy approaches are strongly recommended in clinical guidelines. Pilates exercises are frequently used due to their potential effects on core stability and movement control, while conventional physiotherapy remains a commonly applied treatment method. However, randomized controlled trials directly comparing these interventions are limited. This study aims to compare the short-term effects of reformer Pilates exercises and conventional physiotherapy on pain intensity, functional disability and health-related quality of life in individuals with non-specific chronic low back pain.
Study details
- Official title
- Comparison of Reformer Pilates Exercises and Conventional Physiotherapy on Pain, Disability and Quality of Life in Individuals With Non-Specific Chronic Low Back Pain: A Randomized Controlled Trial
- Conditions
- Interventions
- Other: reformer Pilates exercises
- Other: conventional physiotherapy group
- Sponsor
- Uskudar University
- Start date
- 2026-02-28
- Primary completion
- 2026-04-30
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Healthy volunteers
- true
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: Individuals aged between 18 and 65 years * Diagnosis of non-specific chronic low back pain lasting at least 12 weeks * Average low back pain intensity ≥3 on the Numeric Rating Scale (NRS) during the last week * Ability to participate in exercise sessions three times per week * Providing written informed consent Exclusion Criteria: * Specific causes of low back pain (tumor, infection, inflammatory rheumatic disease, vertebral fracture) * Radiculopathy or significant neurological deficits (progressive motor loss, severe sensory deficit, cauda equina syndrome) * History of lumbar spine surgery within the past 6 months or current surgical indication * Participation in regular Pilates or structured exercise programs within the last 3 months * Severe cardiopulmonary disease or uncontrolled hypertension contraindicating exercise * Pregnancy or early postpartum period * Severe psychiatric or cognitive disorders affecting study compliance * Participation in another physiotherapy or rehabilitation program during the study period
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07543952