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Efficacy of different rehabilitation regimens after total knee replacement: a prospective randomized controlled study

Efficacy of different rehabilitation regimens after total knee replacement: a prospective randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068865
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Knee osteoarthritis

Interventions

experimental group:Tele-rehabilitation equipment
Conrol group:Traditional paper rehabilitation program

Sponsors

Xi'an Honghui Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The patient was 18-75 years old with primary unilateral or bilateral knee osteoarthritis; 2. Primary unilateral total knee replacement; 3. Good physical condition and tolerance to surgery; 4. The ability and conditions to use smart phones; 5. Patients voluntarily participate in clinical trials and can fully cooperate with all trial procedures.

Exclusion criteria

Exclusion criteria: (1) Previous history of open hip or knee surgery; (2) unplanned secondary surgery or revision surgery; (3) with ankylosing spondylitis, rheumatoid arthritis and other inflammatory diseases; (4) severe cardiopulmonary disease or neuromuscular disease; (5) there is a serious mental illness that cannot cooperate with normal rehabilitation; (6) accompanied by fracture or ligament injury; (7) Patients who underwent surgery on the other knee within 90 days; (8) Patients who cannot normally use mobile terminal devices due to various reasons (such as blindness, no smartphone, no Internet, etc.); (9) Patients who refused to join the experiment; (10) Other doctors think that there are factors affecting the test results, so they are not suitable for participants in the experiment.

Design outcomes

Primary

MeasureTime frame
ROM;

Secondary

MeasureTime frame
Satisfaction;

Countries

China

Contacts

Public ContactJianpeng Wang

Xi'an Honghui Hospital

280771976@qq.com+86 158 0299 1190

Outcome results

None listed

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