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Effect of Hegu and Ciliao acupressure on labor pain

Comparison effect of Hegu and Ciliao acupressure on labor pain and delivery outcome in the first stage of labor in primiparous womencontrolled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201601283860N23
Enrollment
105
Registered
2016-02-05
Start date
2008-07-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Labor pain. Pregnancy, childbirth and the puerperium

Interventions

Intervention 1: Intervention group 1- Hegu acupressure: The subjects of Hegu group were asked to sit in their favorable position and the researcher sat in front of them. As the women notified to have
Intervention group 1- Hegu acupressure: The subjects of Hegu group were asked to sit in their favorable position and the researcher sat in front of them. As the women notified to have pain, the resea
Intervention group 2-Ciliao acupressure:The women of the Ciliao group were asked to sit in their favorable position and the researcher sat behind them in a way to have access to sacral region. As the
Control group: Tthe researcher attended the bedside of the subjects and performed all the routine activities done for the other two groups except applying acupressure. The researcher communicated with

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
19 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age range of 19-35 years; term pregnancy (>37 weeks of gestation); planned vaginal delivery without obstetrical or non-obstetrical complications; fetal vertex presentation; being in active phase of first-stage labor with cervical dilatation of =4 cm; presence of at least three uterine contractures within 10 minutes. Exclusion criterion: unwillingness to continue taking part in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Labor pain. Timepoint: in three cervical dilatation stages (4-5, 6-7, and 8-10 cm), before and after intervention. Method of measurement: numerical rating scale.

Secondary

MeasureTime frame
Mode of delivery. Timepoint: once-after delivery. Method of measurement: Questioner.;Neonatal Apgar Score. Timepoint: 1 and 5 minute after birth. Method of measurement: check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGiti Ozgoli

Shahid Beheshti University Of Medical Sciences

gozgoli@sbmu.ac.irg.ozgoli@gmail.com+98 21 8865 5366

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026