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Completed

NCT Number: NCT05541666

Effect of Emotional Freedom Technique on Postoperative Pain and Anxiety in Patients Undergoing Total Knee Replacement

The purpose of the present study was to examine the effects of the Emotional Freedom Technique on pain and anxiety in the postoperative period of patients who underwent total knee arthroplasty.

Research Hypotheses H1: Emotional freedom technique reduces postoperative pain level in patients undergoing total knee arthroplasty.

H2: Emotional freedom technique reduces postoperative anxiety level in patients undergoing total knee arthroplasty.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Atatürk University

Erzurum, Yakutiye, 25240, Turkey (Türkiye)

About this study

One day before the surgery the patients in both groups will interviewed and the Patient Descriptive Data Form, Visual Analog Scale (VAS) Pain, and State Anxiety Inventory (SAI) will applied. Then, information will given to the experimental group about EFT and the patients' questions will answered. On the first postoperative day between 18.00 and 20.00 the patients in both groups will interviewed to collect the pretest data and VAS Pain, SAI, and Subjective Unit of Experience Scale (SUE) will applied. Then, the EFT steps will explained and demonstrated to the experimental group and a session of EFT will applied. After the EFT, the SUE Scale will re-evaluated without any break. On the second postoperative day between 18.00 and 20.00 the patients in both groups will interviewed again, and the SUE Scale will evaluated. Then, a session of the EFT will applied to the experimental group. After the EFT, VAS Pain, SAI, and SUE will re-applied without any break for post-test data. In the control group VAS Pain, SAI, and SUE will re-applied for post-test data on the second postoperative day between 18.00 and 20.00.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Elective patients undergoing total knee replacement surgery for the first time,
  • Volunteer to participate in the research,
  • 18 years and over,
  • Cognitive level scales are suitable for application,
  • Having no vision, hearing, or speech problems that would prevent communication,
  • Patients who do not have any other disease causing pain and anxiety

Exclusion criteria

  • EFT was applied before,
  • If any complication develops within 3 days before, during, or after the operation,
  • Patients with health problems (fever, infection, deep vein thrombosis, etc.) that prevent the application of the Emotional Freedom Technique were not included in the study.

Treatment and study plan

emotional freedom technique (EFT)

Other

EFT is an energy psychology intervention that utilizes cognitive behavioral therapy, exposure therapy, and acupuncture points to create psychological and physical changes in individuals. It is also referred to as "acupuncture without needles" or an emotional form of acupressure.

Primary outcomes

  1. anxiety level

    Time frame: Post-operative 1st and 2nd day

    On the postoperative 1st day and 2nd day, patient's anxiety status will evaluated with State Anxiety Inventory (SAI)

  2. pain level

    Time frame: Post-operative 1st and 2nd day

    On the postoperative 1st day and 2nd day, patient's pain status will evaluated with Visual Analog Scale (VAS).

Sponsors and collaborators

Lead sponsor

Ataturk University

Other

Registry information

Important dates

Study start
2022
Primary completion
2022
Study completion
2023
First posted
Sep 15, 2022
Registry last updated
Dec 12, 2025

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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