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Effects of dynamic four-point kneeling training on hip bone mineral density in patients with spinal cord injury

Effects of dynamic four-point kneeling training on hip bone mineral density in patients with spinal cord injury

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060576
Enrollment
Unknown
Registered
2022-06-05
Start date
2022-05-22
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Spinal cord injury

Interventions

Dynamic four-point kneeling training group:Dynamic four-point kneeling training
Upright bed training group:Upright bed training
Lower Extremity Robot Training Group:Lower Extremity Robot Training

Sponsors

Jiangsu Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Vital signs are stable and able to complete the training; 2. Age: 18-75 years old, gender is not limited; 3. Traumatic spinal cord injury (including surgical trauma) confirmed by CT or MRI in line with the International Diagnostic Criteria for Neurological Classification of Spinal Cord Injury revised by the American Spinal Cord Injury Society in 2019; 4. The motor plane of spinal nerve injury is T2-T12, AIS spinal cord injury grades A, B, and C; 5. The course of the disease is more than 3 months and less than 2 years; 6. Good cognitive function, MMSE >= 24 points, can understand and actively participate in the training program, agree and sign the informed consent form for this clinical study.

Exclusion criteria

Exclusion criteria: 1. Complications that limit the patient's ability to exercise lower extremity deep vein thrombosis, diabetes, hypertension, coronary heart disease, severe osteoporosis, and female pregnancy; 2. Patients with metabolic bone disease, diabetes, thyroid and parathyroid disease, autoimmune disease, severe liver and kidney disease, malignant tumor and the use of drugs that affect bone metabolism; 3. Menopausal female patients; 4. Patients with early knee fracture, knee arthritis or severe knee pain; 5. The patient has severe orthostatic hypotension when standing 6. The investigator judges that the patient has poor compliance or does not understand the test, and cannot complete the study as required; 7. Participated in other drugs or clinical trials during the same period; 8. Other circumstances that the investigator judges not suitable for inclusion or the patient cannot tolerate the trial.

Design outcomes

Primary

MeasureTime frame
Bone density;Extremity surface electromyography assessment;

Secondary

MeasureTime frame
Sensory score;Lower extremity motor score;Modified Ashworth Classification;

Countries

China

Contacts

Public ContactXue Wang

Jiangsu Provincial People's Hospital

wangxue312@yeah.net+86 13505170199

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026