The Effect of Schroth Method on Pain, Body Awareness and Quality of Life in Adolescent Individuals With Idiopathic Scoliosis
NCT ID: NCT04689295
Last Updated: 2024-07-23
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
40 participants
INTERVENTIONAL
2019-07-01
2021-05-15
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.
Comparison of the Effects of Controlled Schroth Exercise and Home Exercise Programs
NCT04203394
The Effectiveness of Different Exercises in Scoliosis
NCT06716957
Effect of Lyon and Schroth Techniques on Adolescent İdiopathic Scoliosis
NCT05223972
Exercises in Adolescent Idiopathic Scoliosis
NCT04421157
The Efficiency of Different Exercise Methods in Adolescent Idiopathic Scoliosis
NCT05985902
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
NON_RANDOMIZED
SEQUENTIAL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
experiment group
Three dimensional scoliosis therapy method (Schroth) will be applied to the participants for 6 weeks. It consist of 15 different exercises combined with rotational breathing exercise.
exercise programme 1
Schroth three dimensional scoliosis therapy method
control group
Traditional scoliosis exercises will be applied to the participants for 6 weeks. It consist of 6 different exercises
exercise programme 2
Traditional scoliosis exercises
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
exercise programme 1
Schroth three dimensional scoliosis therapy method
exercise programme 2
Traditional scoliosis exercises
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Between the ages of 10-18,
* Primary curvature between 20-40 degrees according to the Cobb method,
* Having C or S type of scoliosis,
* Having back / low-back pain due to scoliosis,
* Those who have not received any previous exercise therapy for scoliosis,
* Volunteering to participate in the study,
* Having the cognitive capacity to cooperate with the directions of the physiotherapist,
* Has not suffered any injuries to the musculoskeletal system in the last 6 months,
* No neurological, orthopedic or cardiopulmonary disorders other than scoliosis diagnosis,
* Young individuals who have not undergone any surgery related to the diagnosis of scoliosis
Exclusion Criteria
* Any disease other than idiopathic scoliosis,
* Individuals who cannot adapt to the directions of the physiotherapist and cannot fulfill the requirements of the exercise program
10 Years
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hacettepe University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Fatih Çelik
principal investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
fatih çelik
Role: STUDY_DIRECTOR
physiotherapist
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Fizyo Omurga
Konya, , 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.
2019/0041
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.