- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05227638
Investigation of the Efficacy of PNF and Schroth Treatment
August 15, 2023 updated by: Mehmet Hanifi Kaya
Investigation of the Efficacy of PNF and Schroth Treatment in Adolescent Idiopathic Scoliosis
our study was to compare the advantages of Schroth and PNF methods used in AIS treatment
Study Overview
Detailed Description
there are studies showing that Schroth and PNF are effective on AIS seperately.
While there are studies showing that Schroth is particularly effective on AIS, the number of studies on PNF is insufficient.
However, no evidence was found comparing the efficacy of Schroth and PNF.
Therefore, the aim of our study was to compare the advantages of Schroth and PNF methods used in AIS treatment
Study Type
Interventional
Enrollment (Actual)
36
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
-
-
-
Kırşehir, Turkey, 40100
- Mehmet Hanifi KAYA
-
-
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
Yes
Description
Inclusion Criteria:
- Participants were between ages 10-18
- Volunteered for the study.
- Diagnosed with adolescent idiopathic scoliosis
- Cobb angle between 10-30 degrees
- 0-3 Risser sign
- Lenke curve type 1
Exclusion Criteria:
- non-idiopathic scoliosis
- previous spinal surgery
- who had exercise contraindications who had rheumatological disease who had mental handicap and who another neuromuscular problem
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: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Schroth group
The Schroth group performed Schroth exercises
|
participants were between ages 10-18, volunteered for the study, were diagnosed with adolescent idiopathic scoliosis, were Cobb angle between 10-30 degrees, were 0-3 Risser sign, and were Lenke curve type 1.
Other Names:
|
|
Active Comparator: PNF group
PNF group (PG) performed "chop and lift" exercises
|
participants were between ages 10-18, volunteered for the study, were diagnosed with adolescent idiopathic scoliosis, were Cobb angle between 10-30 degrees, were 0-3 Risser sign, and were Lenke curve type 1.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cobb angle
Time Frame: 8 week
|
anteroposterior x-ray was taken with the entire spine of the patients standing
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8 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
November 10, 2021
Primary Completion (Actual)
January 22, 2022
Study Completion (Actual)
June 25, 2022
Study Registration Dates
First Submitted
January 27, 2022
First Submitted That Met QC Criteria
January 27, 2022
First Posted (Actual)
February 7, 2022
Study Record Updates
Last Update Posted (Actual)
August 16, 2023
Last Update Submitted That Met QC Criteria
August 15, 2023
Last Verified
August 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-10879717-050.01.04-2542
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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