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Completed

NCT Number: NCT05915650

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

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.

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Key information

Conditions

Pain Neurologic Manifestations Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

45 year–74 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yongmei Zhang

Zunyi, Guizhou, 563000, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed as KOA according to the criteria and undergoing unilateral total knee arthroplasty for the first time;
  • The subjects included in this study were men or women aged 45-74 years;
  • Clear self-cognition, can browse the text by themselves or can answer questions correctly;
  • Those who voluntarily participated in the study and signed an informed consent form after understanding the relevant information of the study;
  • Without serious physical diseases such as heart, liver or kidney;
  • No history of mental illness or drug dependence.

Exclusion criteria

  • Combined with severe trauma in other parts;
  • Accompanied by serious damage to other organs, such as heart and cerebrovascular diseases, lung and kidney diseases;
  • Patients with knee tumor and severe knee deformity who could not complete the rehabilitation;
  • With neurological diseases that limit physical activity;
  • Participating in other investigators during the same period.

Treatment and study plan

pain neuroscience education

Behavioral

Carry out pain neuroscience education intervention for TKA patients

Routine Education

Behavioral

Carry out routine education intervention for TKA patients

Primary outcomes

  1. Visual analogue scale pain score, (VAS)

    Time frame: 3 months after discharge

    Status of pain

Sponsors and collaborators

Lead sponsor

Zunyi Medical College

Other

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Jun 23, 2023
Registry last updated
Jun 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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