Tapping therapy eases Pre-C-Section anxiety in High-Risk pregnancies
NCT ID NCT07436832
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested Emotional Freedom Technique (EFT), a form of tapping on acupressure points, in 62 high-risk pregnant women scheduled for a planned C-section. Half received EFT before surgery, while the other half got standard care. Researchers measured anxiety levels before and after the session, and checked for postpartum depression 21 days after birth. The goal was to see if this simple technique could help reduce stress and improve emotional well-being.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Emotional Freedom Technique (tapping)
- What this could lead to
- If it works, this could offer a simple, drug-free way to reduce anxiety before C-section and lower the risk of postpartum depression in high-risk pregnancies.
- What could go wrong
- This is a small, single-center study with only 62 participants. Results may not apply to all pregnant women, and the technique's effects can vary widely.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
62 people
The number who actually took part.
- Started
-
Mar 2024
- Finished
-
Oct 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Participants meeting the following criteria will be included in the study: Identified as at-risk pregnancies according to the Ministry of Health Risk Assessment Form, Able to speak and understand Turkish, Aged between 18 and 45 years, Have a planned cesarean delivery decision, Have a gestational age of 36 weeks or more, Have a State Anxiety Inventory (STAI-State) mean score of 37 or higher, Voluntarily agree to participate in the study. Exclusion Criteria Participants meeting any of the following criteria will be excluded from the study: Pregnant women evaluated between March 1, 2024 and September 30, 2024 at Ankara Etlik City Hospital, Perinatology Clinic, who decline voluntary participation, Pregnant women classified as low-risk according to the Ministry of Health Risk Assessment Form, Younger than 18 years or older than 45 years, Those who undergo vaginal delivery, Pregnant women with a gestational age of 35 weeks or less, Those with a State Anxiety Inventory (STAI-State) mean score of 36 or lower, Pregnant women with any psychiatric disorder or diagnosis, Those unable to speak or understand Turkish, Participants who withdraw from the study at any stage at their own request.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
mersin University
Mersin, Turkey (Türkiye)
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