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Emotional Freedom Technique (EFT) Applied to Postmenopausal Women on Sleep and Quality of Life

The Effect of Emotional Freedom Technique (EFT) Applied to Postmenopausal Women on Sleep and Quality of Life: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06578715
Enrollment
80
Registered
2024-08-29
Start date
2024-10-01
Completion date
2024-11-01
Last updated
2024-10-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Menopause Related Conditions

Brief summary

The study will be conducted as a randomized controlled experimental study to determine the effects of the Emotional Freedom Technique (EFT) applied to women in menopause on sleep quality and quality of life. It will be conducted with 80 women between the ages of 45-64, registered in a family health center in a city in the east of Turkey, who have been in menopause for at least one year and volunteer to participate in the study. EFT will be applied to the women to be included in the experimental group in the study once a week, a total of four times in a month. The Participant Information Form, Utian Quality of Life Scale and Pittsburgh Sleep Quality Scale prepared by the researchers in line with the literature information will be used in the collection of research data.

Detailed description

The study will be conducted as a randomized controlled experimental study to determine the effects of the Emotional Freedom Technique (EFT) applied to women in menopause on sleep quality and quality of life. It will be conducted with 80 women between the ages of 45-64, registered in a family health center in a city in the east of Turkey, who have been in menopause for at least one year and volunteered to participate in the study. The simple randomization method will be selected as the randomization method in the study in order to provide an equal number of samples in two groups. A random number table will be created in a computer environment using the httpp://www.randomizer.org/website for the 80 participants to be sampled, with numbers from 1 to 80 in two groups. It will be decided by tossing a coin to determine which group the groups should be in. The names on the list will be evaluated according to the group corresponding to that order in the table, and accordingly, 40 women will be assigned to the experimental group and 40 women will be assigned to the control group. EFT will be applied to the women to be included in the experimental group in the study once a week, a total of four times in a month. When the research is completed, the data of the experimental and control groups (coded as X and Y) will be transferred to the computer environment by a statistician independent of the research and the data will be analyzed and the findings will be reported. Our research is planned to be conducted as a single-blind study in which the statistician will be blinded. The Participant Information Form, Utian Quality of Life Scale and Pittsburgh Sleep Quality Scale prepared by the researchers in line with the literature information will be used in the collection of research data. Pre-Test Data will be collected between September-October 2024, the interim measurement after the EFT intervention will be made between October-November 2024, and the final measurement will be made between November-December 2024.

Interventions

BEHAVIORALEmotional Freedom Technique

EFT basically involves serial tapping on acupuncture points, no needles are used, there is no invasive procedure, there are affirmation suggestions, it is an easy, painless, simple but effective method that can be done in minutes. It is realized by applying kinetic energy to certain meridians on the head and chest with the fingertips. The points where the tapping is done are the end points of the meridians in the body. They are located symmetrically on both sides of the body. Since these points are close to the skin surface, they are points that are more easily reached than the deeper buried parts of the meridians. While applying pressure with the fingertips, the individual needs to focus on the problem that bothers him/her. Another thing that needs to be done at the same time is for the person to make positive suggestions to himself/herself vocally.

Sponsors

Ataturk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Randomized controlled trial

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

* Volunteering to participate in the study, * Being able to read and write in Turkish, * Women between the ages of 45-64 who have not had menstrual bleeding for at least one year (women under the age of 65 who have entered natural menopause), * Not being diagnosed with a psychiatric disease, * Not using Hormone Replacement Therapy (HRT), * Not using antidepressants, antihistamines, benzodiazepines, hypnotics and narcotics, etc., * Not using any complementary and alternative medicine (such as Reiki, phytoestrogens, acupressure). * Scoring '5 and above' on the Pittsburgh Sleep Quality Scale

Exclusion criteria

* Starting to use Hormone Replacement Therapy after starting the study, * Starting to use antidepressants, antihistamines, benzodiazepines, hypnotics and narcotics, etc., * Starting to use any complementary and alternative medicine method, * Voluntarily leaving the study.

Design outcomes

Primary

MeasureTime frameDescription
Quality of life levels during menopause1 monthThe difference between the Utian Quality of Life Scale pretest and posttest mean scores of women in both groups. The lowest score that can be obtained from the scale is 23, and the highest score is 115. An increase in the scale score indicates an increase in the quality of life.
Quality of sleep levels during menopause1 monthThe difference between the Utian Quality of Life Scale pretest and posttest mean scores of women in both groups. The sleep quality of individuals whose total scale score is 5 points or less is considered good; the sleep quality of individuals whose score is above 5 points is considered bad.

Contacts

Primary ContactAslı SİS ÇELİK
aslisis@atauni.edu.tr05434668242
Backup ContactDerya BİNGÖL
dbingol@bingol.edu.tr+905356413930

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026