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The Effect of Acupressure on Pain Intensity in the First Stage of Labor

The Effect of BL25 Acupressure on Pain Intensity in the First Stage of Labor, And Birth outcome in Pregnant Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240121060761N1
Enrollment
90
Registered
2024-02-07
Start date
2024-07-04
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

The effect of BL25 acupressure on pain intensity in the first stage of labor, and birth outcome in pregnant women.

Interventions

Intervention 1: Intervention group:BL25 acupressure group, intervention in BL25 acupressure points in dilatations of 4-5, 7-6 and 8-10 cm for 20 minutes and a total of 60 minutes, during uterine contr

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: pregnant women (do not have more than one vaginal delivery) Do not have a history of more than one miscarriage Gestational age between 37-42 weeks (according to ultrasound before 12 weeks or LMP) Single ton , Vertex Presentation Dilatation 4-5 cm (at the beginning of the active phase of labor) The presence of at least three contractions in 10 minutes The appropriateness of the pelvic position Failure to use analgesic drugs (chemical or herbal) in the last 8 hours Absence of chronic disease such as cardiovascular disease, kidney disease, joint rheumatism and epilepsy Not suffering from a known mental illness No history of unfortunate events, such as the death of a spouse or a close relative during pregnancy Absence of complications during pregnancy such as pre-eclampsia, chorioamnionitis, etc. Absence of obstetric complications (such as decollement, abnormal fetal heart rate, etc.) upon entering the study

Exclusion criteria

Exclusion criteria: Mother's unwillingness to continue participating in the study Emergency caesarean section (after registration) Occurrence of adverse outcomes (placental detachment, fetal distress, lack of progress in labor) (after registration) Use of other non-pharmacological pain reduction methods (after registration)

Design outcomes

Primary

MeasureTime frame
The pain intensity of the first stage of labor in pregnant women is measured by a numerical pain rating scale. The pain intensity scale is a number between zero and 10, where zero indicates no pain and 10 indicates the most severe pain. Timepoint: Pain intensity is measured before the intervention, and immediately after the end of the intervention, in cervical dilatations of 4-5 cm, 6-7 cm and 8-10 cm. Method of measurement: The pain intensity of the first stage of labor is measured with a numerical pain rating scale. The pain intensity scale is a number between 0 and 10, where 0 represents no pain and 10 represents the most severe pain.

Secondary

MeasureTime frame
The duration of the second stage of labor. Timepoint: From the completion of cervical dilatation until the complete expulsion of the fetus. Method of measurement: Observation and examination checklist.;The duration of the third stage of labor. Timepoint: From the exit of the fetus to the complete exit of the placenta and membranes. Method of measurement: Observation and examination checklist.;Need to resuscitate the baby. Timepoint: Postpartum. Method of measurement: Observation and examination checklist.;Apgar score of the baby. Timepoint: Postpartum. Method of measurement: Observation and examination checklist.;Bishop's score. Timepoint: In cervical dilatations of 4-5, 6-7 and 8-10 cm. Method of measurement: Observation and examination checklist.;Frequency of uterine contractions. Timepoint: In cervical dilatations of 4-5, 6-7 and 8-10 cm. Method of measurement: Observation and examination checklist.;Intensity of uterine contractions. Timepoint: In cervical dilatations of 4-5, 6-7 and 8-10 cm. Method of measurement: Observation and examination checklist.;Duration of uterine contractions. Timepoint: In cervical dilatations of 4-5, 6-7 and 8-10 cm. Method of measurement: Observation and examination checklist.;Need oxytocin. Timepoint: Postpartum. Method of measurement: Observation and examination checklist.;The need for pharmaceutical pain relief methods. Timepoint: Postpartum. Method of measurement: Observation and examination checklist.;Mother's satisfaction with pain relief. Timepoint: Postpartum. Method of measurement: Likert's questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdieh Aly

Shahid Beheshti University of Medical Sciences

mahdieh-aly@sbmu.ac.ir+98 11 4245 0274

Outcome results

None listed

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