Actively Recruiting
The Individualized Stepwise Treatment Mode of Adolescent Idiopathic Scoliosis Using a Comprehensive Health Management Platform
Led by Hangzhou Medical College · Updated on 2026-02-23
76
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating treatment approaches for adolescent idiopathic scoliosis (AIS), a condition causing sideways curvature of the spine, using a comprehensive health management platform. The study compares conventional treatment based on 2016 SOSORT guidelines with an individualized stepwise treatment model developed through data analysis. The goal is to assess which approach better manages scoliosis progression and related outcomes in adolescents aged 12 to 16. Participants are randomly assigned to either the control group receiving routine treatment or the intervention group receiving personalized care via the health management platform. This platform helps determine the best treatment plan for each individual, which may include massage therapy, posture guidance, Schroeder's gymnastics therapy, and bioelectric stimulation therapy. Both groups will be observed and treated over a 4-month period. During the study, researchers will measure changes in spinal curvature using Cobb angles before and after intervention, evaluate the accuracy of new screening methods at multiple points, and assess depression levels with the Hamilton Depression Scale. Participants will be monitored for 4 months during treatment and followed up to 8 months after intervention to track outcomes. The study aims to improve scoliosis management and enhance quality of life for adolescents with AIS.
CONDITIONS
Brief Title
Personalized Prevention and Treatment Strategies for Adolescent Idiopathic Scoliosis Via a Comprehensive Health Management Platform
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of mild to moderate adolescent idiopathic scoliosis with a Cobb angle less than 45 degrees
- Age between 12 and 16 years old
- No history of mental illness and normal communication skills
- Ability to read and write
- Signed informed consent by the patient or their family
You will not qualify if you...
- History of scoliosis caused by trauma or surgery
- Cognitive impairment
- Severe dysfunction of heart, liver, kidney, or other organs
- Malignant tumors or immune diseases
- Other malignant diseases
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 months
Participants receive either conventional treatment according to established guidelines or an individualized treatment plan through a health management platform, including therapies such as massage, posture guidance, Schroeder's gymnastics, and bioelectric stimulation.
Visits scheduled according to treatment plan and platform guidance
Duration - Up to 8 months after treatment ends
Participants are monitored after the treatment period to assess outcomes such as Cobb angles and depression scores.
Visits at 4 months and 8 months post-treatment
Trial Site Locations
Total: 1 location
1
the Affiliated Zhejiang Provincial People's Hospital to Hangzhou Medical College.
Hangzhou, Zhejiang, China, 311000
Actively Recruiting
Research Team
X
Xinyun Dr LI, Doctor
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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