Application of PNE in Postoperative Pain Management of Patients With Primary Total Knee Arthroplasty

Pain Clinical Trial

Official title:

Application of PNE in Postoperative Pain Management of Patients With Primary Total Knee Arthroplasty

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05915650
• Other study ID #: KLLY-2020-147
• Status: Completed
• Phase: N/A
• Start date: December 1, 2020
• Est. completion date: December 1, 2021

Study information

• Verified date: June 2023
• Source: Zunyi Medical College
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study intends to carry out pain neuroscience education intervention for TKA patients to clarify the effect of this method on the degree of postoperative pain, the incidence of pain catastrophizing, kinesiophobia, and knee joint function rehabilitation in TKA patients, so as to provide a basis for clinical nursing of such patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: December 1, 2021
• Est. primary completion date: December 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 45 Years to 74 Years

Eligibility

Inclusion Criteria:

1. Patients diagnosed as KOA according to the criteria and undergoing unilateral total knee arthroplasty for the first time;

2. The subjects included in this study were men or women aged 45-74 years;

3. Clear self-cognition, can browse the text by themselves or can answer questions correctly;

4. Those who voluntarily participated in the study and signed an informed consent form after understanding the relevant information of the study;

5. Without serious physical diseases such as heart, liver or kidney;

6. No history of mental illness or drug dependence.

Exclusion Criteria:

1. Combined with severe trauma in other parts;

2. Accompanied by serious damage to other organs, such as heart and cerebrovascular diseases, lung and kidney diseases;

3. Patients with knee tumor and severe knee deformity who could not complete the rehabilitation;

4. With neurological diseases that limit physical activity;

5. Participating in other investigators during the same period.

Related Conditions & MeSH terms

• Pain
• Pain, Postoperative

Intervention

Behavioral:
• Pain Neuroscience Education
Carry out pain neuroscience education intervention for TKA patients
• Routine Education
Carry out routine education intervention for TKA patients

Locations

Country	Name	City	State
China	Yongmei Zhang	Zunyi	Guizhou

Sponsors (1)

Lead Sponsor	Collaborator
Zunyi Medical College

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual analogue scale pain score, (VAS)	Status of pain	3 months after discharge