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Construction and Evaluation of a Postoperative Rehabilitation Exercise Protocol for Patients Following Partial Meniscectomy

Construction and Evaluation of a Postoperative Rehabilitation Exercise Protocol for Patients Following Partial Meniscectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124256
Enrollment
Unknown
Registered
2026-05-09
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

meniscus injury

Interventions

Intervention group:On the day after surgery, during integrated physician–nurse ward rounds, the research team developed personalized rehabilitation plans for patients in the intervention group by dele

Sponsors

The First Affiliated Hospital of Nanhua University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria 1. Patients undergoing partial meniscectomy; 2. Individuals without physical disabilities; 3. Proficient in using smartphones and the WeChat application; 4. Voluntary participation in the study.

Exclusion criteria

Exclusion criteria: Exclusion Criteria 1.Patients with psychiatric disorders or impaired communication abilities; 2. Those with comorbid malignant tumors; 3. Individuals with a history of prior knee surgery; 4. Patients with severe arthritis; Withdrawal Criteria 1.Participants who refuse to continue the study; 2.Individuals who voluntarily withdraw due to personal reasons during the intervention period; 3. Participants who experience physical discomfort during the intervention period and are deemed unsuitable to continue.

Design outcomes

Primary

MeasureTime frame
Range of Motion;

Secondary

MeasureTime frame
Lysholm Knee Score;VAS Score;Complication Rate;

Countries

China

Contacts

Public ContactLi Xiaoshan

The First Affiliated Hospital of Nanhua University

lxiaoshan99@163.com+86 189 9880 1153

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026