Health TrialsbyHealthPanel

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

ConditionAdolescent Idiopathic Scoliosis (AIS)
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age3-18
SponsorHangzhou Medical College

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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.

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Conventional treatment

    Procedure/Surgery

    Patients will randomly assigned to routine treatment group (control group) and individualized treatment model group (intervention group). All patients will observed and intervened for 4 months. Patients in the control treatment group will follow the treatment plan in the 2016SOSORT guidelines

  • intervention treatment

    Behavioral

    Patients will be input into the health management platform. The optimal treatment scheme will be then determined through data calculation and sent to individuals (or their families) or schools for implementation under the guidance of the platform. It is important to note that the specific treatment plan varied from person to person. Patients were observed and intervened for a period of 4 months. 1. Massage therapy 2. Posture guidance 3. Schroeder\'s gymnastics therapy 4. Bioelectric stimulation therapy

Treatment groups

76 Participants
are divided into 2 treatment groups
Group A: controlNo intervention 0 interventions
Group B: interventionExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Number of Cobb angles

X-rays were used to check the number of Cobb angles before and 4 months after the intervention to observe the improvement of scoliosis

Time frame
4 months before the intervention and 4 months after the intervention
2

Accuracy of new screening modalities

The new screening method "general examination + forward flexion test + scoliosis measuring instrument" was used for examination, and the data results before and 4 months after intervention were compared with the X-ray examination results to verify its accuracy.

Time frame
4 months before and after the intervention, 4 months after the end of the intervention, and 8 months after the end of the intervention
3

Hamilton Depression Volume

Depression status was rated using the Hamilton Depression Rating Scale

Time frame
4 months before and after the intervention, 4 months after the end of the intervention, and 8 months after the end of the intervention

Secondary outcomes

Other outcomes

Sponsors and contacts

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Hangzhou Medical College

Lead sponsor

Source ClinicalTrials.gov
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