Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
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 \-

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07783776). StuddyBuddy aggregates publicly available trial information.