Conventional treatment: 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: 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
Study 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.
Eligibility
Sex
ALL
Min age
3 Years
Max age
18 Years
Healthy volunteers
Accepted
Inclusion Criteria:
1. The diagnosis of moderate and mild AIS, with a Cobb angle measuring less than 45°;
2. The age range of 12 to 16 years old;
3. Participants are required to have no history of mental illness, possess normal communication skills, and be proficient in reading and writing;
4. Signed informed consent by the patient or their family.
Exclusion Criteria:
Patients who fulfill any of the following conditions will be excluded a clear history of inducement, such as diseases caused by trauma, surgery, cognitive impairment, severe dysfunction of heart, liver, kidney and other organs, and malignant tumors, immune diseases and other malignant diseases.
Primary outcome measure(s)
Number of Cobb angles — 4 months before the intervention and 4 months after the intervention X-rays were used to check the number of Cobb angles before and 4 months after the intervention to observe the improvement of scoliosis
Accuracy of new screening modalities — 4 months before and after the intervention, 4 months after the end of the intervention, and 8 months after the end of the intervention 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.
Hamilton Depression Volume — 4 months before and after the intervention, 4 months after the end of the intervention, and 8 months after the end of the intervention Depression status was rated using the Hamilton Depression Rating Scale
Trial sites (1)
Facility
City
Region
Status
the Affiliated Zhejiang Provincial People's Hospital to Hangzhou Medical College.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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