Prevalence of Myofascial Pain Syndrome in Adolescent Idiopathic Scoliosis
NCT ID: NCT05185050
Last Updated: 2022-06-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
168 participants
OBSERVATIONAL
2021-10-10
2022-04-25
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Investigation of Conservative Treatment on Adolescent Idiopathic Scoliosis Patients.
NCT04921813
The Relationship of Cervical Sagittal Parameters With Pain and Disability in Cervical Myofascial Pain Syndrome
NCT05225571
Effectiveness of Kinesiotaping in Adolescent Idiopathic Scoliosis
NCT06901752
This Cross-sectional Study Investigates the Relationship Between Different Curve Patterns in Adolescent Idiopathic Scoliosis (AIS) and the Distribution of Foot Pressure. It Aims to Determine Whether Coronal and Sagittal Curve Patterns Are Associated With Asymmetries in Plantar Pressure Distribution
NCT07172048
Investigation of the Efficiency of Spinal Mobilization in Patients With Adolescent Idiopathic Scoliosis
NCT05765019
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
1. Regional pain complaint
2. Pain or sensory change reflected from trigger points to a specific area 3. Palpable taut band in accessible muscles
4\. Extreme tenderness at one point along the taut band 5. Decreased range of motion that can be measured As for the Minor Criteria;
1. Complaint of clinical pain and/or sensory change on pressurized palpation of the trigger point
2. Local twitch response of the tender point on the taut band with palpation and needling 3. Reduction of pain by injection of the tender point or stretching of the muscle Five major and at least 1 minor criteria are required for the clinical diagnosis of myofascial pain syndrome.
Patients with a previous history of surgery for scoliosis and neuromuscular scoliosis were excluded from the study.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
AIS with MPS
the participants who has Cobb angle above 10 degrees and diagnosed with myofascial pain syndrome
physical examination and measurement of spinal alignment
physical examination for scoliosis and myofascial pain syndrome, measurement of spinal coronal and sagittal alignment in X-ray, and pain intensity (with Visual analog scale) if necessary (for MPS group)
AIS with no pain
the participants who has Cobb angle above 10 degrees and without pain
physical examination and measurement of spinal alignment
physical examination for scoliosis and myofascial pain syndrome, measurement of spinal coronal and sagittal alignment in X-ray, and pain intensity (with Visual analog scale) if necessary (for MPS group)
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
physical examination and measurement of spinal alignment
physical examination for scoliosis and myofascial pain syndrome, measurement of spinal coronal and sagittal alignment in X-ray, and pain intensity (with Visual analog scale) if necessary (for MPS group)
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* diagnosed as adolescent idiopathic scoliosis
* agreed to participate in the study
Exclusion Criteria
* any surgical treatment for scoliosis or spine.
10 Years
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Kanuni Sultan Suleyman Training and Research Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Merve Damla Korkmaz
Specialist Doctor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Merve Damla Korkmaz, 1
Role: PRINCIPAL_INVESTIGATOR
Kanuni Sultan Suleyman Training and Research Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kanuni Sultan Süleyman Training and Research Hospital
Istanbul, Kucukcekmece, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
KAEK/2020.07.128
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.