Development and Application of a Patient Engagement Program for Postoperative Pain Management Following Total Knee Arthroplasty

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300075105

Enrollment

Unknown

Registered

2023-08-25

Start date

2023-08-26

Completion date

Unknown

Last updated

2023-08-28

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

Conditions

total knee arthroplasty

Interventions

Intervention Group:The interventionl group (n=37) will receive patient engagement in postoperative pain management program and standard care

Control Group:standard care

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who had been diagnosed as having knee arthritis ;have an elective admission for primary, unilateral, TKA surgery;they are adults (aged >18 years) ;get informed consent or ability to complete questionnaires

Exclusion criteria

Exclusion criteria: Patients who will undergo TKA again in 1 month;have major postoperative complications

Design outcomes

Primary

Measure	Time frame
pain-related patient-reported outcomes;	—

Secondary

Measure	Time frame
Self-efficacy;knee function;Time for patients to get out of bed for the first time after surgery;Length of stay ;types and dosages of postoperative analgesics;adverse events;	—

Countries

China

Contacts

Public ContactXuelian LIU

Zhujiang Hospital, Southern Medical University

lxlkuaile@126.com+86 180 2860 1568

Outcome results

None listed

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