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An empirical study on intelligent wearable devices and multi-terminal Internet rehabilitation management platform for middle-aged and elderly degenerative osteoarthrosis

Research and demonstration of key technologies for intelligent rehabilitation of degenerative bone and joint diseases in the middle-aged and elderly

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086425
Enrollment
Unknown
Registered
2024-07-01
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Degenerative bone and joint diseases in the middle-aged and elderly

Interventions

Test group:Wear wearable motion monitoring terminal equipment ( sensor) and download and install supporting applications (which can return motion data) after guidance
guide rehabilitation training.
Control group:Guide rehabilitation training.

Sponsors

Luoyang Orthopedic Hospital of Henan Province. Orthopedic Hospital of Henan Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Patients with osteoarthritis of knee joint 1) the diagnostic criteria of western medicine for knee osteoarthritis; 2) patients aged 45-65; 3) be able to use smartphones and smart wearable devices independently; 4) be confirmed as KL1-3 by X-ray examination; 5) those who have not received manipulation, intra-articular injection or acupuncture in the past 3 months; 6) No mental or neurological diseases, no severe liver and renal insufficiency, cardiovascular disease, no history of acute cerebral infarction and angina pectoris; 7) voluntarily participated in this trial and signed the informed consent form. 2.Patients with lumbar disc herniation 1) meet the diagnostic criteria of western medicine for prolapse of lumbar intervertebral disc; 2) patients aged from 45 to 65 years old; 3) be able to use smartphones and smart wearable devices independently; 4) confirmed by lumbar MRI or CT examination of lumbar vertebrae as L4 paddle 5 or L5/S1 intervertebral disc herniation; 5) those who have not received manipulation or acupuncture treatment in the past 3 months; 6) voluntarily participate in this trial and sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with severe diseases such as spine, hip, ankle or other causes of dyskinesia; 2) patients with severe underlying diseases, such as heart failure, respiratory failure, chronic renal insufficiency, etc.; 3) previous surgery history of lumbar vertebrae, hip joint and knee joint; 4) severe hearing, vision and cognitive impairment; 5) incomplete case data; 6) those who are intolerable or unsuitable for rehabilitation due to pain.

Design outcomes

Primary

MeasureTime frame
The Western Ontario and McMaster Universities Osteoarthritis Index (Only evaluated in patients with knee osteoarthritis);HSS Rating Scale (Only evaluated in patients with knee osteoarthritis);Osweatry Low Back Pain Disability Questionnaire (only for patients with lumbar disc herniation);Japanese Orthopedic Association Low back pain score scale (only for patients with lumbar disc herniation);

Secondary

MeasureTime frame
Numeric Rating Scale;The Medical OutcomesStudy 36-Short Form Health Survey;Functional exercise compliance scale;

Countries

China

Contacts

Public ContactXiang Yang, Cao

Luoyang Orthopedic Hospital of Henan Province. Orthopedic Hospital of Henan Province

809251369@qq.com+86 138 3883 6188

Outcome results

None listed

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