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Construction and Optimization of an Adaptive AI Rehabilitation Training Monitoring Platform for Lower Limb Alignment Abnormalities in Adolescents

Construction and Optimization of an Adaptive AI Rehabilitation Training Monitoring Platform for Lower Limb Alignment Abnormalities in Adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001318
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Alignment Abnormalities of Lower Limbs in Adolescents and Associated Diseases

Interventions

Experimental group:The traditional practice scheme, recommended by AI, is used for targeted training, conducted once daily, with each session lasting 30 minutes. The doctor's end combines multimodal a
Control Group:Routine traditional exercises are combined with necessary core muscle and coordination training. Progress is reported to the doctor once a week, and the doctor adjusts the plan based on

Sponsors

Wangjing Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 18 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the above diagnostic criteria for genu varum/valgum; (2) Patients without genu varum/valgum caused by trauma or rheumatic diseases; (3) Patients who have not undergone surgery or brace treatment; (4) Patients aged between 7 and 18 years, with no restriction on gender; (5) Patients who agree to participate and sign the informed consent form. Subjects who satisfy all of the above five criteria can be included as cases.

Exclusion criteria

Exclusion criteria: (1) Patients with severe liver and kidney diseases, cardiovascular diseases, or mental illness; (2) Patients with diseases causing secondary genu varum/valgum, or with neurological, muscular, or skeletal diseases; (3) Patients who have undergone surgery or orthotic treatment; (4) Patients with attention deficit or other conditions preventing them from following instructions to complete rehabilitation; (5) Patients with a recent history of trauma. Note: If any of the above options is "Yes," the subject cannot be enrolled in the study.

Design outcomes

Primary

MeasureTime frame
Tibiofemoral angle;

Secondary

MeasureTime frame
Gait Analysis;Foot Arch Index and Center of Gravity Shift;Foot pressure value;SF-36 Quality of Life Index;The completion rate of patients undergoing rehabilitation.;

Countries

China

Contacts

Public ContactHan Tao

Wangjing Hospital of China Academy of Chinese Medical Sciences

zygkhantao@aliyun.com15811096120

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026