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Clinical Study on the Improvement of Adult Idiopathic Scoliosis by Sling Exercise Therapy Training Combined With Conventional Exercise Therapy

Therapeutic Efficacy of Combined Sling Exercise Therapy and Conventional Exercise Therapy in Adult Idiopathic Scoliosis:A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07109037
Enrollment
30
Registered
2025-08-07
Start date
2025-04-25
Completion date
2025-06-27
Last updated
2025-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Scoliosis, Adult

Keywords

Sling exercise training, Exercise therapy, Adult, Idiopathic scoliosis

Brief summary

This study aims to compare the effects of suspension exercise therapy combined with conventional exercise therapy and conventional exercise therapy alone on pain, Cobb angle, functional impairment, and quality of life in adult patients with idiopathic scoliosis.

Interventions

Conventional exercise therapy includes four exercises: the little swallow flying exercise, the hip bridge exercise, back muscle stretching, and relaxation. It is performed once a day, 45 minutes .

OTHERSuspension training and conventional exercise therapy

Suspension training alternates with conventional exercise therapy. It is conducted every other day, 45 minutes each time, 2-3 times a week for four consecutive weeks. Elastic ropes for suspension training are chosen based on patients' body mass: single - strand for those with body mass ≤ 30 kg and double - strand for those with body mass \> 30 kg. Suspension slings are placed on the head, lower back, and pelvis, and non-elastic rope slings on the ankles. Lower the lifting bed so that the vertical distance from the ankles to the bed surface is about 25-30 cm.

Sponsors

Southwest Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* In the anteroposterior and lateral X-ray films of the spine in the standing position, the Cobb angle is ≥10° and \<40° * The age ranges from 18 to 75 years old * No previous history of surgery * Not wearing a corrective brace

Exclusion criteria

* Having mental illnesses * Having severe cognitive and communication disorders * Having severe cardiopulmonary dysfunction or cardiovascular diseases * Having adult degenerative and secondary scoliosis

Design outcomes

Primary

MeasureTime frame
Cobb angleThe measurements and evaluations were conducted on the first day of treatment and after the completion of the 30 - day treatment respectively.

Secondary

MeasureTime frameDescription
Oswestry Disability IndexThe evaluation was conducted on the first day of treatment and after the completion of the 30-day treatment respectively.The Oswestry Disability Index (ODI) scale consists of 10 dimensions, such as walking, sitting, standing, and self-care ability. Each dimension is scored on a scale from 0 to 5 points, yielding a maximum total score of 50 points and a Minimum total score of 0 points. A higher score on the ODI indicates a more severe degree of functional impairment. The results of the ODI can be classified into four grades: a score range of 0%-20% suggests mild impairment; 21%-40% indicates moderate impairment; 41%-60% represents severe impairment; and 61%-100% reflects extremely severe functional impairment.
Pain score (Visual Analogue Scale, VAS)The evaluation was conducted on the first day of treatment and after the completion of the 30-day treatment respectively.The Visual Analogue Scale(VAS) is a 0-10 scale, with 0 signifying no pain and 10 representing the most excruciating pain one can conceive. When administering the VAS, ensure that the graduated side of the scale is not visible to the patient. Then, ask the patient to mark the point on the ruler that reflects their current pain level. After that, the physician will assign a score according to the marked position. Based on the obtained score, pain can be classified as follows: a score of ≤3 indicates mild pain, 4-6 corresponds to moderate pain, and a score of ≥ 7 represents severe pain.
Quality of life assessment (Scoliosis Research Society - 22 questionnaire, SRS - 22)The evaluation was conducted on the first day of treatment and after the completion of the 30-day treatment respectively.The Scoliosis Research Society-22 (SRS-22) questionnaire was employed to assess the QOL of patients. It evaluates quality of life across five dimensions: functional activities, pain, self -image, psychological state, and treatment satisfaction. Each item is scored from 1 to 5, and the total score, with a maximum of 110 and minimum of 0 , reflects a better QOL as it increases.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026