COMPARISON OF THE EFFECTIVENESS OF CLINICAL AND HOME-BASED SCHROTH EXERCISES ON ADOLESCENT IDIOPATHIC SCOLIOSIS INDIVIDUALS
NCT ID: NCT06187623
Last Updated: 2024-01-02
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.
RECRUITING
30 participants
OBSERVATIONAL
2023-12-15
2024-03-04
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.
Effect of Lyon and Schroth Techniques on Adolescent İdiopathic Scoliosis
NCT05223972
The Effectiveness of Different Exercises in Scoliosis
NCT06716957
Investigation of the Efficacy of PNF and Schroth Treatment
NCT05227638
Impact of Long-Term Schroth Exercises on Scoliosis Severity and Quality of Life in Braced AIS Individuals
NCT06500806
Comparison of the Effects of Controlled Schroth Exercise and Home Exercise Programs
NCT04203394
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The 30 participants who will participate in the study will be between the ages of 10-18 and their Cobb angle will vary between 25-45 degrees. Consent forms will be obtained from all participants participating in the study.
Cervical Relocation Test to measure participants' proprioception; Y-Balance Test will be used for dynamic balance, evaluation of trunk rotation angle with a scoliometer, Spinal Appearence Questionnaire for cosmetic deformity perception, Bad-Sobernheim Stress Questionnaire will be used for brace stress.
Demographic information such as age (years), weight (kg), height (cm), lower extremity length (cm), primary curvatures, daily brace use time (hours), brace use frequency of the people who agreed to participate in the study were collected. corset revision The number and use of insoles (yes or not) will be questioned.
The Cervicocephalic Relocation Test developed by Revel will be used to evaluate cervical proprioception. Blindfolded subjects will be seated on a chair with a backrest, 90cm away from the wall on which a circular target board is hung. They will be asked to sit as far back in the chair as possible, placing their arms on their laps, and leaning on the back of the chair. Each subject has a laser pointer attached to their head and their eyes will be covered with a sleep mask. The person's head position will be placed on the target board by the therapist, showing the laser zero point, and 5 seconds will be given to remember this point. Subjects will experience the test with their eyes open before starting the experiment. After concentrating on this reference position for a few seconds, the patient will be asked to move the head in the previously shown directions (flexion, extension) for 5 repetitions and return to the reference point. The distance between the starting head position and the ending head position will be calculated as the angular result by placing it in the formula angle = tan -1 \[Distance between the start and the end cm/90 cm\].
Dynamic Balance- Y Balance Test After the foot of the party to be tested is placed behind the red line on the platform, they will be asked to push the distance indicator in all three directions (anterior, postromedial and posterolateral) as far as possible with the foot in the air. After two trials are made in each direction before the test, three measurements will be taken for each direction during the test phase. For each direction, the total score obtained by dividing the best value of the three maximum distances by the leg length and multiplying by 100 will be calculated and noted. The test will be terminated when the person lifts the heel of the tested foot standing on the platform to maintain balance during the test, loses contact with the distance indicator, uses it as support to restore the lost balance and cannot return to the starting position.
Scoliometer, individuals will be asked to stand upright, looking forward with their feet parallel and adjacent to each other, and then the individual will be told that they should lean forward with their hands and feet together, keeping their body parallel to the ground. During the evaluation, the spinous processes will be monitored with a scoliometer, starting from the cervical region to the lumbar region.
For quality of life assessment; Bad Sobernheim Stress Questionnaire and Scoliosis Appearance Questionnaire were used. Evaluations will be answered twice, before and after.
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.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Home based Group
15 patients in the home-based group and their parents will be informed about the treatment program. Exercise training will be given to individuals by a physiotherapist trained in ISST- International Schroth 3-Dimensional Scoliosis Therapy.
Individuals in this group will be included in an exercise program 1 day a week (8 sessions) accompanied by a physiotherapist for 8 weeks. Each exercise session will last 50 minutes. Patients will be asked to do the given home exercises on the remaining 6 days of the week.
Home based exercise
15 patients in the home-based group and their parents will be informed about the treatment program. Exercise training will be given to individuals by a physiotherapist trained in ISST- International Schroth 3-Dimensional Scoliosis Therapy.
Individuals in this group will be included in an exercise program 1 day a week (8 sessions) accompanied by a physiotherapist for 8 weeks. Each exercise session will last 50 minutes. Patients will be asked to do the given home exercises on the remaining 6 days of the week.
Clinic based Group
15 patients and their parents in the clinic-based group will be informed about the treatment program. Exercise training will be given to individuals by a physiotherapist trained in ISST- International Schroth 3-Dimensional Scoliosis Therapy.
Individuals in this group will be included in an exercise program 3 days a week (24 sessions) with a physiotherapist for 8 weeks. Each exercise session will last 50 minutes. Patients will be asked to do the given home exercises on the remaining 4 days of the week.
Clinic based exercise
15 patients and their parents in the clinic-based group will be informed about the treatment program. Exercise training will be given to individuals by a physiotherapist trained in ISST- International Schroth 3-Dimensional Scoliosis Therapy.
Individuals in this group will be included in an exercise program 3 days a week (24 sessions) with a physiotherapist for 8 weeks. Each exercise session will last 50 minutes. Patients will be asked to do the given home exercises on the remaining 4 days of the week.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Clinic based exercise
15 patients and their parents in the clinic-based group will be informed about the treatment program. Exercise training will be given to individuals by a physiotherapist trained in ISST- International Schroth 3-Dimensional Scoliosis Therapy.
Individuals in this group will be included in an exercise program 3 days a week (24 sessions) with a physiotherapist for 8 weeks. Each exercise session will last 50 minutes. Patients will be asked to do the given home exercises on the remaining 4 days of the week.
Home based exercise
15 patients in the home-based group and their parents will be informed about the treatment program. Exercise training will be given to individuals by a physiotherapist trained in ISST- International Schroth 3-Dimensional Scoliosis Therapy.
Individuals in this group will be included in an exercise program 1 day a week (8 sessions) accompanied by a physiotherapist for 8 weeks. Each exercise session will last 50 minutes. Patients will be asked to do the given home exercises on the remaining 6 days of the week.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being diagnosed with Adolescent Idiopathic Scoliosis (AIS),
* COBB angles should be between 20 and 45 degrees,
* Risser sign being between 0-5,
* Having brace treatment given by the doctor.
Exclusion Criteria
* Having had spine surgery,
* Stating that you will not comply with the corset period prescribed by the doctor,
* Having serious cardiopulmonary problems that will prevent them from exercising,
* Individuals and parents did not agree to sign the consent form required to participate in the study.
10 Years
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Uskudar University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ipek Yurttaş
Physiotherapist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
ipek yurttaş
Role: PRINCIPAL_INVESTIGATOR
Üsküdar University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Uskudar University
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Physiotherapy rehabilitation
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.