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Limb InjuryNCT07066371

The Effect of Emotional Freedom Technique on Patients Receiving Preventive Foot Care

A study testing Emotional freedom technique in people with Limb Injury and Limb Ischemia, run by Bitlis Eren University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

It is planned to examine the effect of the emotional liberation technique on the anxiety level in patients who receive preventive foot wound care and treatment in the postoperative period. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Limb Injury, Limb Ischemia, Complication Diabetic
What is being tested?
Emotional freedom technique
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Apr 2025to 30 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Must be 18 years old or older
  • Must have no communication problems
  • Must have had surgery for a foot ulcer

Who cannot join

  • Having any auditory or mental problems
  • Having difficulty/not being able to apply Emotional Freedom Technique (EFT)
  • Wanting to leave the study

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Bitlis Eren University

    Bitlis, 13100

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Emotional Freedom Technique on Anxiety Levels in Patients Receiving Preventive Foot Wound Care and Treatment in the Postoperative Period

It is planned to examine the effect of the emotional liberation technique on the anxiety level in patients who receive preventive foot wound care and treatment in the postoperative period.

H0: The emotional liberation technique has no effect on the anxiety level in patients who receive preventive foot wound care and treatment in the postoperative period.

H1: The emotional liberation technique has an effect on reducing anxiety in patients who receive preventive foot wound care and treatment in the postoperative period.

Read the detailed description

The type of the study is a prospective randomized controlled clinical research model. The study design is a pre-test-post-test control group experimental trial. Data will be collected by the researchers through face-to-face interviews.

Patient identification form, state and trait anxiety scale will be applied to the experimental and control group patients as part of the pre-test. After the patients are given EFT training, they will be asked to apply it twice a week for 1 month. EFT videos and brochures will be given to the patients. 1 EFT session is applied for an average of 15 minutes. No intervention will be applied to the control group patients and the clinic's routine patient care and applications will be continued. State and trait anxiety scale will be applied to the experimental and control group patients as part of the post-test.

*After the data collection process is completed, EFT training will be given to the control group patients if they wish. EFT videos and brochures will be given to the patients. It will be stated to the patients that they can contact the researchers by phone for information/support regarding the applications.

Emotional freedom technique application is an application that works on cognitive and energetic levels. For this reason, in the application of the emotional freedom technique, exposure therapy is applied to individuals first. Exposure therapy is the comparison of individuals with the situation called trigger, which creates a stress response in the individual, during the application. The individual is reminded of the trigger and the individual is made conscious and aware of the discomfort. This situation activates the amygdala and creates a threat warning.

Emotional Freedom Technique Application Guidelines

  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 SUDS again
Being tested
Emotional freedom technique
Keywords
post-operative, emotional freedom technique, anxiety, wound care
Medical subject headings
Diabetes Complications, Postoperative Complications, Patient Compliance, Anxiety Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Emotional freedom techniqueBehavioural

    Emotional Freedom Technique Application Guidelines

    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 SUDS again
Study groups in NCT07066371
Study groupRoleWhat they receive
Emotional freedom techniqueExperimentalAfter the patients are given EFT training, they will be asked to apply it twice a week for 1 month. EFT videos and brochures will be given to the patients. 1 EFT session is applied for an average of 15 minutes. Emotional Freedom Technique Application Guidelines 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 SUDS again
Receives: Behavioral: Emotional freedom technique
Standard of CareNo interventionAs part of the pre-test, the patient introduction form, state and trait anxiety scale will be applied to the control group patients. The intervention will not be applied to the control group patients and the clinic's routine patient care and practices will continue. As part of the post-test, the state and trait anxiety scale will be applied to the control group patients again. *After the data collection process is completed, EFT training will be provided to the control group patients upon their request. EFT videos and brochures will be provided to the patients. It will be stated to the patients that they can contact the researchers by phone for information/support regarding the practices.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. anxiety level

    State and Trait Anxiety Scale:

    The adaptation and arrangement of the scales to Turkish was made by Necla Öner and Le Compte. Both scales consist of 20 items and are graded on a 4-point Likert scale. Scoring is done between 1-4. The scores obtained from both scales theoretically vary between 20 and 80. A high score indicates a high level of anxiety, a low score indicates a low level of anxiety.

    Measured: After receiving EFT training, patients will be asked to apply it twice a week for one month. Each EFT session lasts approximately 15 minutes. Measurements will be taken over one month.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jul 2025
  2. Study start15 Apr 2025
  3. Primary completion1 Sep 2025
  4. Study completion30 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Crossover
Model description
It will be conducted as a randomized controlled experimental study in a pretestpost- test control group experimental model.
Masking
None (open label)
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07066371
Sponsor's protocol ID
okutan 10
Status last verified
Feb 2026
First submitted
3 Apr 2025
Last updated
25 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Emotional freedom technique in people with Limb Injury and Limb Ischemia, run by Bitlis Eren University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

anxiety level (time frame: After receiving EFT training, patients will be asked to apply it twice a week for one month. Each EFT session lasts approximately 15 minutes. Measurements will be taken over one month.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Feb 2026.

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