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The Effect of Emotional Freedom Technique on Mental Well-Being and Stress Level in Pregnant Women

The Effect of Emotional Freedom Technique Applied to Women With Risky Pregnancy on Mental Well-Being and Stress Level

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06181903
Enrollment
120
Registered
2023-12-26
Start date
2024-02-28
Completion date
2024-08-31
Last updated
2024-07-09

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

Conditions

Pregnant at Risk

Keywords

Pregnant, Well-being, Mental health, Stress, Emotional Freedom Technique

Brief summary

Emotional freedom technique will be applied to women with risky pregnancy. Emotional freedom technique group and control groups each consisted of 60 pregnant women.

Detailed description

Objective In this experimental study, it was aimed to examine the effect of emotional freedom technique applied to women with risky pregnancy on mental well-being and stress levels. Materials and Methods: This randomized controlled study will be conducted between February 2024 and August 2024 in Kahramanmaraş Necip Fazıl City Hospital Obstetrics and Gynecology Annex Building Obstetrics Outpatient Clinics with a total of 120 risk pregnant women (60 EFT, 60 control). EFT will be applied in the study. Women in the EFT group will receive EFT four times at one-week intervals. Pretest data will be obtained by filling out the Personal Information Form, Warwick-Edinburgh Mental Well-Being Scale (WEMWB), Prenatal Distress Scale - Revised Version before the Emotional Freedom Technique application. After the interventions, post-test data will be obtained by completing the Warwick-Edinburgh Mental Well-Being Scale (WEMWB), Prenatal Distress Scale - Revised Version. In addition, the Subjective Units of Experience (SUE) scale will be administered before and after each EFT intervention.

Interventions

Control group

Sponsors

Kahramanmaras Sutcu Imam University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years of age or older, * Graduated from at least primary school * Volunteering to participate in the research, * Primiparous, * Pregnant women who do not have conditions such as infection, wound, scar in the tapping areas. * Pregnant women who meet any of the criteria in the Ministry of Health Risk Assessment Form for Pregnancy.

Exclusion criteria

* Pregnant women who participated in EFT or other antenatal classes/programs during the study period. * Those who did not want to continue participating in the study, * Those with a psychological problem according to the pregnant women's statements.

Design outcomes

Primary

MeasureTime frameDescription
Assessment of the level of Mental Well-BeingThe Warwick-Edinburgh Mental Well-Being Scale will be administered to two groups of pregnant women on day one (first interview)The scale is a 14-item, self-report style scale. The scale consists of positive items including hedonic and eudaimonic dimensions of mental well-being, optimism, feeling useful, relaxation, interest in other people, being energetic and lively, coping with problems, clear thinking, feeling good, feeling close to other people, self-confidence, decision-making, love, interest in new things and being cheerful. The scale covers psychological well-being and subjective well-being and deals with the positive mental health of individuals. The scale is a five-point Likert scale with a minimum score of 14 and a maximum score of 70. Scoring of the scale is as follows: strongly disagree (1), disagree (2), somewhat agree (3), agree (4), strongly agree (5). All items of the scale are positive. High scores on the scale indicate high mental well-being.
Assessment of prenatal distress levelThe Prenatal Distress Scale - Revised Version will be administered to two groups of pregnant women on day one (first interview)The scale determines pregnant women's social relationships, their physical and emotional symptoms during pregnancy, and their level of anxiety about themselves and their babies. The scale items have options ranging from Not at all (0), A little (1) and Very much (2), and the total score is obtained by summing the scores of the answers given to the scale items. A minimum score of 0 and a maximum score of 34 points are obtained from the scale. An increase in the total score obtained from the scale indicates an increase in the level of prenatal distress perceived by pregnant women.
Determining the level of anxietyThe Subjective Units of Experience (SUE) scale will be administered to two groups of pregnant women on day one (first interview)Subjective Units of Experience (SUE) will be applied to determine the anxiety level of pregnant women. The SUE is used to determine the intensity of one's emotions at the beginning and end of the therapy. The scale is scored between -10 and +10, with negative numbers indicating negative/unpleasant experiences and positive numbers indicating positive/pleasant experiences.

Countries

Turkey (Türkiye)

Contacts

Primary ContactEsra KARATAŞ OKYAY, PhD
esrakaratas44@hotmail.com05432125225
Backup ContactEsra GÜNEY, PhD
esra.guney@inonu.edu.tr05432064063

Outcome results

None listed

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