NCT05541666

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 7, 2022

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

September 13, 2022

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 15, 2022

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 15, 2022

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 2, 2023

Completed
Last Updated

December 12, 2025

Status Verified

December 1, 2025

Enrollment Period

6 months

First QC Date

September 13, 2022

Last Update Submit

December 5, 2025

Conditions

Keywords

AnxietyEmotional Freedom TechniquePainTotal Knee Replacement

Outcome Measures

Primary Outcomes (2)

  • anxiety level

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

    Post-operative 1st and 2nd day

  • pain level

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

    Post-operative 1st and 2nd day

Study Arms (2)

Experimental group

EXPERIMENTAL

EFT will applied to the patients in the experimental group on the 1st and 2nd days after surgery.

Other: Emotional Freedom Technique (EFT)

Control Group

NO INTERVENTION

Patients in the control group will received no treatment other than the clinic's routine patient care.

Interventions

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.

Experimental group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Elective patients undergoing total knee replacement surgery for the first time,
  • Volunteer to participate in the research,
  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Atatürk University

Erzurum, Yakutiye, 25240, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Anxiety DisordersPain

Condition Hierarchy (Ancestors)

Mental DisordersNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Dilek Gürçayır

    Ataturk Univesity

    PRINCIPAL INVESTIGATOR
  • Dilek Gürçayır

    Ataturk University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: This study was planned as a parallel, two-arm randomized controlled trial (RCT).
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research assistant

Study Record Dates

First Submitted

September 13, 2022

First Posted

September 15, 2022

Study Start

March 7, 2022

Primary Completion

September 15, 2022

Study Completion

January 2, 2023

Last Updated

December 12, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations