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Completed
NCT07783776
Yintang Acupressure During Labor in Primiparous Women
Conditions: Labor Pain, Anxiety
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: Yes
Phase: NA
Enrollment: 104
Sponsor: Inonu University
Location: İnönü University Malatya Malatya
Summary
This randomized controlled study evaluated whether acupressure applied to the Yintang point during labor affects labor duration, pain, anxiety, and childbirth satisfaction in primiparous women. A total of 104 women were randomly assigned to either the Yintang acupressure group or the sham light-touch control group, with 52 participants in each group.
Participants in the intervention group received five acupressure sessions during labor and the early postpartum period. Participants in the control group received routine midwifery care and light touch at a non-therapeutic forehead location. Labor duration, pain intensity, anxiety, and childbirth satisfaction were compared between the groups.
Eligibility Criteria
Inclusion Criteria:
* Primiparous women
Aged 18 years or older
In the active phase of labor with cervical dilation of 5-6 cm at enrollment
Term singleton pregnancy
Fetus in vertex presentation
No known fetal congenital anomaly
Intact and healthy skin at the forehead area where acupressure or sham light touch was applied
Provided written informed consent to participate
Exclusion Criteria:Known sensitivity or intolerance to acupressure or touch at the application area
Use of pharmacological pain-control methods, including analgesics, sedatives, or epidural analgesia, before enrollment
High-risk pregnancy, including preeclampsia or diabetes
History of a diagnosed neurological or psychiatric disorder
Evidence of fetal distress
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Source: ClinicalTrials.gov (NCT07783776). StuddyBuddy aggregates publicly available trial information.