NCT06816576

Brief Summary

The aim is to examine the effect of Emotional Freedom Technique on death anxiety in patients with postoperative cancer phobia. The hypotheses of the study are as follows: H0: Emotional Freedom Technique has no effect on postoperative death anxiety in patients with cancer phobia. H1: Emotional Freedom Technique has a positive effect on postoperative death anxiety in patients with cancer phobia.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2025

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

First Submitted

Initial submission to the registry

February 2, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

February 10, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

February 10, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 28, 2025

Completed
12 days until next milestone

Study Completion

Last participant's last visit for all outcomes

October 10, 2025

Completed
Last Updated

January 5, 2026

Status Verified

December 1, 2025

Enrollment Period

8 months

First QC Date

February 2, 2025

Last Update Submit

December 31, 2025

Conditions

Keywords

Death AnxietypostoperativeEmotional Freedom Techniquecancer phobia

Outcome Measures

Primary Outcomes (1)

  • death anxiety

    Death Anxiety Scale: The scale developed by Templer was translated into Turkish by Sarıkaya and Baloğlu. The scale consists of 20 items. High scores indicate high death anxiety.

    After coming to the clinic after surgery and their condition becoming stable, the death anxiety scale was applied to the patients as a pre-test. Three days later, the death anxiety scale was applied as a post-test.

Study Arms (2)

Intervention Group

EXPERIMENTAL

After coming to the clinic after surgery and after their condition was stable, the patients were given the patient introduction form, subjective discomfort unit, cancer anxiety scale and death anxiety scale as a pre-test. The researchers provided EFT training to the patients and asked them to apply EFT. After an average of 3 days, the subjective discomfort unit, cancer anxiety scale and death anxiety scale were applied as a post-test.

Other: Emotional Freedom Technique

Control Group

NO INTERVENTION

After coming to the clinic after surgery and after their condition was stable, the patient introduction form, subjective discomfort unit, cancer anxiety scale and death anxiety scale were applied as a pre-test. No intervention was made to the control group patients outside the clinical protocol. After an average of 3 days, the subjective discomfort unit, cancer anxiety scale and death anxiety scale were applied as a post-test.

Interventions

Emotional Freedom Technique application; It is an application that works on cognitive and energetic levels. Emotional Freedom Technique Application Instructions 1. Determination of Subjective Units of Disturbance (SUD) 2. Preparation or setup 3. Application of appropriate acupuncture points in order 4. 9-Gamut: An application that allows the two hemispheres of the brain to be stimulated simultaneously 5. Application of appropriate acupuncture points in order again 6. Control of the differentiation in the level of discomfort with Subjective Units of Disturbance again

Intervention Group

Eligibility Criteria

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

You may qualify if:

  • Being over 18 years of age,
  • Having had oncological surgery,
  • Having no visual or auditory problems,
  • Having no psychiatric problems.

You may not qualify if:

  • Not accepting to participate in the study or wanting to leave,
  • Being under 18 years of age,
  • Having been previously diagnosed with cancer.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bitlis Eren University

Bitlis, 13100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Postoperative ComplicationsEmotional RegulationNecrophobiaPathophobia

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsSelf-ControlSocial BehaviorBehavior

Study Officials

  • Şerafettin OKUTAN, Dr.

    Bitlis Eren University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
CROSSOVER
Model Details: It will be conducted as a randomized controlled experimental study in a pre-testpost- test control group experimental model.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator, Assistant Professor Şerafettin OKUTAN, Surgical Nursing, Faculty of Health Sciences, Bitlis Eren University

Study Record Dates

First Submitted

February 2, 2025

First Posted

February 10, 2025

Study Start

February 10, 2025

Primary Completion

September 28, 2025

Study Completion

October 10, 2025

Last Updated

January 5, 2026

Record last verified: 2025-12

Locations