Hacettepe University, Faculty of Physical Therapy and Rehabilitation
Ankara, Samanpazarı, 06100, Turkey (Türkiye)
NCT Number: NCT07418983
The use of various muscle energy techniques to address fascial restrictions, in addition to three-dimensional correction within scoliosis-specific exercise approaches, suggests that these exercises may have different effects on thoracolumbar fascia thickness. This may, in turn, lead to varying impacts on low back pain and functional improvement. Therefore, the aim of this study is to investigate the effects of different scoliosis-specific exercise approaches on thoracolumbar fascia thickness, low back pain, and function in individuals with idiopathic lumbar scoliosis and chronic low back pain.
Looking for future studies?
Notify Me11 year–24 year
All sexes
Interventional
Not applicable
Ankara, Samanpazarı, 06100, Turkey (Türkiye)
Low back pain is the most common complaint among individuals with lumbar scoliosis. In a study conducted in Japan, the prevalence of low back pain was reported as 34.7%, which was nearly three times higher than that observed in students without scoliosis. Pain resulting from scoliosis leads to a high level of functional disability, which consequently reduces quality of life.
The thoracolumbar fascia consists of dense connective tissue layers separated by loose connective tissue that allows the tight layers to glide over one another during trunk movement. It provides a mechanical connection between the lumbar spine and several muscles, including the transversus abdominis, portions of the latissimus dorsi, and the internal oblique muscles. In individuals with idiopathic scoliosis, thickening of this fascia has been observed, and it has been reported that this thickening is further increased in the presence of chronic low back pain. Fascial thickening in individuals with scoliosis has been proposed as a potential factor contributing to both pain and movement restrictions.
In the treatment of scoliosis, scoliosis-specific exercise approaches are widely used. These approaches typically include various active self-correction strategies (based on the location, shape, and magnitude of the curve) and individually tailored exercises. Some scoliosis-specific exercise approaches incorporate techniques such as contract-relax, myofascial release, trigger point therapy, and joint mobilization to eliminate muscular and fascial restrictions that impede movement, thereby preparing individuals with scoliosis for three-dimensional correction. In addition, these exercises have been reported to exert positive therapeutic effects on pain and quality of life in individuals with idiopathic scoliosis.
The use of various muscle energy techniques to address fascial restrictions, in addition to three-dimensional correction within scoliosis-specific exercise approaches, suggests that these exercises may have different effects on thoracolumbar fascia thickness. This may, in turn, lead to varying impacts on low back pain and functional improvement. Therefore, the aim of this study is to investigate the effects of different scoliosis-specific exercise approaches on thoracolumbar fascia thickness, low back pain, and function in individuals with idiopathic lumbar scoliosis and chronic low back pain.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants in the SEAS group will receive one supervised 60-minute clinical session per week for 8 weeks, combined with a 40-minute home exercise program performed 6 days per week according to the SEAS protocol.
Participants in the FITS group will receive one supervised 60-minute clinical session per week for 8 weeks, along with a 40-minute home exercise program performed 6 days per week following the FITS method.
Time frame: Baseline and 8 weeks after the intervention
Thoracolumbar fascia thickness will be measured using ultrasound at two bilateral points, located 2-3 cm lateral to the L3 spinous processes. Thoracolumbar fascia thickness will be measured in millimeters using ultrasound imaging. Fascia organization will be classified using a Likert scale as follows: very disorganized, somewhat disorganized, somewhat organized, and very organized, according to the method described in the study protocol.
Time frame: Baseline and 8 weeks after the intervention
Pain intensity will be assessed using a 100-mm Visual Analog Scale (0 = no pain, 100 = worst imaginable pain).
Time frame: Baseline and 8 weeks after intervention
Pain quality will be measured using the Short-Form McGill Pain Questionnaire (SF-MPQ) sensory and affective subscale scores. Higher scores indicate worse pain quality.
Time frame: Baseline and 8 weeks after the intervention
Functional disability will be assessed using thethe Revised Oswestry Disability Questionnaire (RODQ), a 10-item questionnaire evaluating the impact of low back pain on daily activities using a 5-point Likert scale.
Time frame: Baseline and 8 weeks after the intervention
Health-related quality of life was evaluated using the Scoliosis Research Society-22 (SRS-22) questionnaire, which is specifically designed and validated for individuals with scoliosis. This instrument consists of 22 items covering five domains: function/activity, pain, self-image, mental health, and satisfaction with management. Higher scores obtained from the questionnaire indicate a better health status and improved quality of life across the evaluated domains.
Hacettepe University
Other
Comparative Effects of Two Exercise Approaches on Thoracolumbar Fascia and Clinical Outcomes in Idiopathic Lumbar Scoliosis With Chronic Low Back Pain: A Randomized Controlled Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06774898
Back Pain, Bone Diseases
Paris, Île-de-France Region, France
View Trial DetailsNCT06789016
Bone Diseases, Musculoskeletal Diseases
Poznan, Wielkopolska, Poland
View Trial DetailsNCT04637802
Acute Pain, Bone Diseases
Seattle, Washington, United States
View Trial DetailsNCT05961228
Bone Diseases, Musculoskeletal Diseases
Haifa, Israel
View Trial Details