Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03497520
Other study ID # B-1701/377-305
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date March 29, 2018
Est. completion date December 2024

Study information

Verified date April 2024
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of asymmetric spinal stabilization exercise on scoliosis


Description:

- Design: Prospective study - Setting: hospital rehabilitation department - Intervention: Participants are educated asymmetric spinal stabilization exercise along scoliosis curve patterns, including the location of apex and the direction of convexity. After performing asymmetric spinal stabilization exercise, participants are compared the main outcome measures. - Main outcome measures: Cobb angle, Apical vertebral rotation in Adam's test, surface EMG, Scoliosis Research Society-22(SRS-22) quastionnaire


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 150
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years and older
Eligibility Inclusion Criteria: - who have idiopathic scoliosis, showing at Cobb's angle over 10 degrees on X-ray Exclusion Criteria: - Patients who underwent spinal surgery - Patients with spinal scoliosis due to cerebral palsy, muscle paralysis, polio, congenital spinal abnormalities - Patients observed with Cobb's angle less than 10 degrees, over 40 degrees - Patients complaining of acute low back pain

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
asymmetric spinal stabilization exercise
The patients were educated to strengthening weakness side of spinal muscle, as asymmetric spinal stabilization exercise(ASSE) before teach ASSE, the investigators will evaluate Cobb angle, Apical vertebral rotation in Adam's test, surface EMG, Scoliosis Research Society-22(SRS-22) quastionnaire for evaluation of scoliosis severity after perform ASSE, the investigators will evaluate Cobb angle, Apical vertebral rotation in Adam's test, surface EMG, Scoliosis Research Society-22(SRS-22) quastionnaire for evaluation of scoliosis severity

Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam Gyeonggi-do

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary cobb angle measure lateral curve of vertebra on spine x-ray AP view through study completion, an average of 6 months
Primary Apical vertebral rotation angle of trunk rotation in Adam's test through study completion, an average of 1 year
Primary surface electromyography surface muscle contraction of bilateral spinal muscle on T7, T12, L3 through study completion, an average of 6 months
Secondary Scoliosis Research Society-22(SRS-22) quastionnaire five different factors (pain, self-image/appearance, function/activity, mental health, and satisfaction with management, 5 = best; 1 = worst)the minimum and maximum score range is from 5 to 25 through study completion, an average of 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT04914507 - A Prospective Analysis of Long-Term Clinical Outcomes and 3D Spine Growth in Anterior Vertebral Body Tethering N/A
Not yet recruiting NCT05830825 - PMCF (Post-Market Clinical Follow-up) Study on The Tether™ in UK (United Kingdom)
Terminated NCT03676712 - The Effect of Flexible Thoracolumbar Brace on Idiopathic Scoliosis, Prospective, Randomized, Open-label Trial N/A
Terminated NCT04538092 - Complex Spine Enhanced Recovery After Surgery (ERAS) N/A
Completed NCT04669327 - Hip and Knee Moments Normal and With Scoliosis
Completed NCT05033171 - Rod Shape Changing After Scoliosis Correction Surgery N/A
Recruiting NCT04505579 - The Tether™ - Vertebral Body Tethering System Post Approval Study
Recruiting NCT04047225 - POSTOPERATIVE OPIOID-SPARING EFFECT OF INTRAOPERATIVE PAIN MONITORING USING THE ANALGESIA NOCICEPTIVE INDEX (ANI) DURING IDIOPATHIC SCOLIOSIS CORRECTION IN CHILDREN. N/A
Recruiting NCT06086431 - Dexamethasone vs. Dexmedetomidine for ESPB in Pain Management After Pediatric Idiopathic Scoliosis Surgery Phase 4
Not yet recruiting NCT05039255 - Acute Effects of Self-correcting Movement on the Balance and Spine of Patients With Scoliosis.
Completed NCT03820895 - Vitamin D Levels in Adolescent Idiopathic Scoliosis
Recruiting NCT05045014 - Evaluation of Vestibular Dysfunction or Visuospatial Perception in Individuals With Idiopathic Scoliosis
Recruiting NCT05011734 - Rapid Postoperative Recovery Pathway in Adolescent Idiopathic Scoliosis.
Active, not recruiting NCT04343170 - Effect of Ultra-short-term Treatment of Patients With Iron Deficiency or Anemia Undergoing Adolescent Scoliosis Correction N/A
Completed NCT04677140 - Hip Related Functional Limitations in Individuals With Idiopathic Scoliosis
Recruiting NCT06093477 - Studying Melatonin and Recovery in Teens N/A
Completed NCT06063447 - Does Adolescent Idıopathic Scoliosis Cause Pelvic Floor Dysfunction?
Recruiting NCT06417944 - The Effect of Three-dimensional Exercise (Schroth Exercise) on Diaphragm Thickness in Adolescent Idiopathic Scoliosis Patients
Recruiting NCT05938959 - Erector Spinae Plane Block for Pediatric Idiopathic Scoliosis Surgery Phase 4
Completed NCT05298371 - The Effect of Sitting and Standing Posture on Trunk Rotation in Patients With Idiopathic Scoliosis