Trunk Proprioception in Adolescent Idiopathic Scoliosis
NCT ID: NCT05326256
Last Updated: 2023-04-19
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
NA
21 participants
INTERVENTIONAL
2022-02-02
2023-04-17
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
* To investigate trunk proprioception in all three planes in individuals with adolescent idiopathic scoliosis (AIS),
* To investigate the pelvis orientation sense in all three planes in individuals with adolescent idiopathic scoliosis,
* To investigate whether trunk proprioception and pelvis orientation sense are improved with Physiotherapy Scoliosis Specific Exercises (PSSE) in AIS,
* To investigate whether trunk proprioception and pelvis orientation sense are improved with vestibular exercise training to be added to PSSE exercises in AIS,
* Comparison of the effects of different exercise training on trunk proprioception and pelvis orientation sense in AIS
* To examine the parameters that may be associated with the improvement of trunk proprioception of different exercise training (health-related quality of life, perception of cosmetic deformity, scoliosis-related clinical features such as Cobb angle, axial trunk rotation, curve type, etc.).
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Augmented Reality-Based Exercise Training in Adolescents With Idiopathic Scoliosis
NCT07201103
The Effects of Scoliosis-Specific Exercises Before Surgery
NCT04357561
The Effect of Schroth Exercises on Pulmonary Function in Adolescent Idiopathic Scoliosis
NCT05505695
Scoliosis-Specific Exercises on Physical Fitness Parameters
NCT07249502
The Effect of Exercise on Paravertebral Muscle Thickness and Quality of Life in Adolescent Idiopathic Scoliosis
NCT07250295
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
As the control group; healthy peers with the same characteristics as the exercise groups will be included and they have a negative result of Adam's forward bending test, they do not have any postural disorders.
As a result of the randomization to be applied to the individuals, they will be divided into two groups: PSSE exercise group and vestibular exercise group (vestibular exercises added to PSSE exercises).
Initial assessments will be given to all individuals. Exercise training groups will participate in a 45-minute exercise session with the supervisor, twice a week for 12 weeks. Before exercise training, individuals and their parents will be informed about education and daily life activities.
Apart from the exercises performed under the supervision of a physiotherapist, individuals will be given a home exercise program, and the family and the individual will be asked to keep a diary to evaluate their compliance with the exercise, and the exercise compliance will be evaluated with a phone call every week.
When the exercise training is completed, the training groups will be evaluated as post-training assessments.
In the statistical analysis of data; the values of the control group will be used as normative and will be compared with the data of individuals with scoliosis. The data of the training groups before and after the training program will be compared, and the data of the different exercise groups will be compared with each other.
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.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
PSSE Group
Physiotherapy Scoliosis Specific Exercises (PSSE), 45-minute exercise session with the supervisor, twice a week for 12 weeks
Exercise training- PSSE
Barcelona Scoliosis Physical Therapy School (BSPTS) method exercises
Vestibular Exercise Group
Vestibular exercises to be added to PSSE exercises, 45-minute exercise session with the supervisor, twice a week for 12 weeks
Exercise training- PSSE with vestibular exercises
Vestibular exercises added to Barcelona Scoliosis Physical Therapy School (BSPTS) exercises
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Exercise training- PSSE
Barcelona Scoliosis Physical Therapy School (BSPTS) method exercises
Exercise training- PSSE with vestibular exercises
Vestibular exercises added to Barcelona Scoliosis Physical Therapy School (BSPTS) exercises
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Aged 10-18,
* Have Physiotherapy Scoliosis Specific Exercises (PSSE) indications,
* Individuals and her/his parents volunteered to participate in the study.
Exclusion Criteria
* Have had spinal surgery before,
* Have any mental problems,
* The fact that scoliosis is not idiopathic but has arisen for different reasons (neurological, congenital, etc.),
* The apex of the curve is thoracal-6 vertebrae and above,
* Any neurological, psychiatric, muscular, rheumatic, renal, cardiovascular, pulmonary, tumoral, or orthopedic disease.
10 Years
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hasan Kalyoncu University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Merve Karatel
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hasan Kalyoncu University
Gaziantep, , 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.
2022/008
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.