- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05530850
The Effect of Holistic Corrective Exercise Program
September 21, 2022 updated by: Gonul Elpeze, Hasan Kalyoncu University
The Effect of Holistic Corrective Exercise Program on Kyphosis Degree, Balance and Quality of Life in Kyphotic Adolescent
This study was planned to investigate the effect of holistic approach corrective exercise program on the degree of kyphosis, balance and quality of life in kyphotic adolescents.
A holistic approach corrective exercise program including corrective exercises and postural perception training was applied to one group.
Thoracic region focused exercise program was applied to the other group.
The programs of the exercise groups were applied three days a week, for 12 weeks.
The kyphosis angle of all individuals participating in the study was evaluated using the flexible ruler, the Romberg index measured with balance pedobarography, and the quality of life using the Scoliosis Research Society-22 Questionnaire (SRS-22).
In our study, a decrease in the degree of kyphosis was detected in the holistic approach corrective exercise and thoracic region-focused exercise group after 12 weeks of exercise training (p<0.001), while no change was observed in the control group (p>0.05).
Balance improved after exercise training in the holistic corrective exercise group (p=0.006).
The quality of life increased in the holistic approach corrective exercise and thoracic region focused exercise groups after the training (p<0.001).
The use of postural perception training together with corrective exercise programs in applications for thoracic kyphosis reveals a holistic approach and may increase the effect of the intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
62
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Gazi̇antep
-
Şehi̇tkami̇l, Gazi̇antep, Turkey
- Hasan Kalyoncu Üniversitesi
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
10 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Male individual between the ages of 10-18,
- Kyphosis degree ≥50°,
Exclusion Criteria:
- Rrigid thoracic kyphosis
- Scoliosis with a Cobb angle >10°
- Congenital spine problem,
- Shoulder, pelvis and other spinal injuries
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Holistic Corrective Exercise Program
A holistic approach corrective exercise program including corrective exercises and postural perception training
|
A holistic approach corrective exercise program including corrective exercises and postural perception training,
|
Experimental: Thoracic exercise program
Thoracic region focused exercise program
|
Thoracic region focused exercise program
|
No Intervention: control group
Individuals in the control group were asked to continue their activities of daily living.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Kyphosis angle by using flexible ruler
Time Frame: 12 weeks
|
Flexible ruler
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Balance assesment by using the romberg index
Time Frame: 12 weeks
|
the Romberg index, Pedobarography
|
12 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Quality of Life by using SRS-22
Time Frame: 12 weeks
|
Scoliosis Research Society-22 Questionnaire (SRS-22)
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: GÖNÜL ELPEZE, HKU
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 15, 2022
Primary Completion (Actual)
May 15, 2022
Study Completion (Actual)
June 21, 2022
Study Registration Dates
First Submitted
September 2, 2022
First Submitted That Met QC Criteria
September 2, 2022
First Posted (Actual)
September 7, 2022
Study Record Updates
Last Update Posted (Actual)
September 22, 2022
Last Update Submitted That Met QC Criteria
September 21, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HKU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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