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

NCT ID: NCT05915650

Last Updated: 2023-06-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-12-01

Study Completion Date

2021-12-01

Brief Summary

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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.

Detailed Description

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Conditions

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Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Pain Neuroscience Education Group

Group Type EXPERIMENTAL

Pain Neuroscience Education

Intervention Type BEHAVIORAL

Carry out pain neuroscience education intervention for TKA patients

Routine Education Group

Group Type EXPERIMENTAL

Routine Education

Intervention Type BEHAVIORAL

Carry out routine education intervention for TKA patients

Interventions

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Pain Neuroscience Education

Carry out pain neuroscience education intervention for TKA patients

Intervention Type BEHAVIORAL

Routine Education

Carry out routine education intervention for TKA patients

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

45 Years

Maximum Eligible Age

74 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Zunyi Medical College

OTHER

Sponsor Role lead

Responsible Party

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Yongmei Zhang

Study Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Yongmei Zhang

Zunyi, Guizhou, China

Site Status

Countries

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China

Other Identifiers

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KLLY-2020-147

Identifier Type: -

Identifier Source: org_study_id

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