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Investigation of the Efficacy of PNF and Schroth Treatment

Sponsor
Mehmet Hanifi Kaya (Other)
Overall Status
Completed
CT.gov ID
NCT05227638
Collaborator
Kirsehir Ahi Evran Universitesi (Other)
36
Enrollment
1
Location
2
Arms
5.5
Actual Duration (Months)
6.6
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

our study was to compare the advantages of Schroth and PNF methods used in AIS treatment

Condition or Disease Intervention/Treatment Phase
  • Other: exercise
 N/A

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 Design

Study Type:
Interventional
Actual Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
Investigation of the Efficacy of PNF and Schroth Treatment in Adolescent Idiopathic Scoliosis
Actual Study Start Date :
Nov 10, 2021
Actual Primary Completion Date :
Jan 22, 2022
Actual Study Completion Date :
Apr 25, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Schroth group

The Schroth group performed Schroth exercises

Other: exercise
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:
  • PNF group

    		•
    Active Comparator: PNF group

    PNF group (PG) performed "chop and lift" exercises

    Other: exercise
    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:
  • PNF group

    		•

    Outcome Measures

    Primary Outcome Measures

    1. Cobb angle [8 week]

      anteroposterior x-ray was taken with the entire spine of the patients standing

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    10 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mehmet Hanifi KAYA Kırşehir Turkey 40100

    Sponsors and Collaborators

    • Mehmet Hanifi Kaya
    • Kirsehir Ahi Evran Universitesi

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Mehmet Hanifi Kaya, Lecturer, Kirsehir Ahi Evran Universitesi
    ClinicalTrials.gov Identifier:
    NCT05227638
    Other Study ID Numbers:
    • E-10879717-050.01.04-2542
    First Posted:
    Feb 7, 2022
    Last Update Posted:
    Jul 20, 2022
    Last Verified:
    Jul 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:
    Scoliosis

    Study Results

    No Results Posted as of Jul 20, 2022