RecruitingNot Applicable

Personalized Prevention and Treatment Strategies for Adolescent Idiopathic Scoliosis Via a Comprehensive Health Management Platform

China76 participantsStarted 2025-08-01

Plain-language summary

Spinal cord injury (SCI), leads to functional deficits and complications like neurogenic bladder and deep vein thrombosis, imposing a global annual financial burden. This trial aims to compares Jiaji electroacupuncture (JEA) and scalp electroacupuncture (SEA) in SCI rehabilitation. This randomized controlled trial (RCT) compared JEA and SEA in SCI rehabilitation.

Who can participate

Age range

3 Years – 18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. The diagnosis of moderate and mild AIS, with a Cobb angle measuring less than 45°;
. The age range of 12 to 16 years old;
. Participants are required to have no history of mental illness, possess normal communication skills, and be proficient in reading and writing;
. Signed informed consent by the patient or their family.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Number of Cobb angles

Timeframe: 4 months before the intervention and 4 months after the intervention

Accuracy of new screening modalities

Timeframe: 4 months before and after the intervention, 4 months after the end of the intervention, and 8 months after the end of the intervention

Hamilton Depression Volume

Timeframe: 4 months before and after the intervention, 4 months after the end of the intervention, and 8 months after the end of the intervention

Trial details

NCT IDNCT06314594

SponsorHangzhou Medical College

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-12-01

Contact for this trial

Xinyun Dr LI, Doctor

8618069783240 lxyjasmine2010@163.com

View on ClinicalTrials.gov More Adolescent Idiopathic Scoliosis (AIS) trials

Plain-language summary

Who can participate

Age range

3 Years – 18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. The diagnosis of moderate and mild AIS, with a Cobb angle measuring less than 45°;
. The age range of 12 to 16 years old;
. Participants are required to have no history of mental illness, possess normal communication skills, and be proficient in reading and writing;
. Signed informed consent by the patient or their family.

What they're measuring

Number of Cobb angles

Timeframe: 4 months before the intervention and 4 months after the intervention

Accuracy of new screening modalities

Timeframe: 4 months before and after the intervention, 4 months after the end of the intervention, and 8 months after the end of the intervention

Hamilton Depression Volume

Timeframe: 4 months before and after the intervention, 4 months after the end of the intervention, and 8 months after the end of the intervention