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Development and implementation of a program for the prevention of chronic preoperative pain among patients undergoing total knee arthroplasty

Development and implementation of a program for the prevention of chronic preoperative pain among patients undergoing total knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069615
Enrollment
Unknown
Registered
2023-03-22
Start date
2023-06-17
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

total knee arthroplasty

Interventions

Experimental group:multi-disciplinarity transitional pain service
Control group:Maintain daily exercise and join waiting list

Sponsors

School of Nursing and Rehabilitation, Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Meeting the diagnostic criteria for osteoarthritis disease (2) Initial total knee arthroplasty; (3) Those who were at high-risk of developing chronic pain; (4) Those who have basic reading and writing skills and have no barriers to communication; (5) Basic operation of smart phones; (6) Age =45 years old, informed consent, voluntary principle, and signed informed consent form.

Exclusion criteria

Exclusion criteria: (1) cognitive dysfunction (MMSE <=20); (2) Re-exposure to orthopedic surgery during the follow-up period. (3) with severe cardiac, hepatic, or renal insufficiency, malignancy, etc. (4) with diseases limiting the movement of the lower extremities. (5) Participating in other studies.

Design outcomes

Primary

MeasureTime frame
The incidence of chronic preoperative pain;pain degree;

Secondary

MeasureTime frame
fear of movement;knee joint function;social participation;

Countries

China

Contacts

Public ContactLuan Xiaorong

School of Nursing and Rehabilitation, Shandong University

199162000814@sdu.edu.cn+86 185 6008 0208

Outcome results

None listed

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