Skip to content

Effect of TENS on the reduction of labor pain

Evaluation and comparison Effect of Transcutaneouse Electrical Nerve Stimulation (TENS) in Lumbar & acupuncture points in reducing Labor Pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20080826001096N6
Enrollment
84
Registered
2018-05-02
Start date
2018-01-05
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Delivery. Assisted single delivery, unspecified

Interventions

Intervention 1: Placebo control (Inactive lumbar and acupuncture TENS group): Lumbar and acupuncture points electrodes will be connected to the study participants and will receive very little stimulat

Sponsors

Research vice-chancellorship, Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Pregnant women aged 35-18 years old Having reading and writing skills The gestational age: 41-37 weeks Single pregnancy Cephalic fetal presentation Latent phase of labor (dilatation less than 4-3 cm)

Exclusion criteria

Exclusion criteria: Use of epidural analgesia or other anesthetics within 24 hours before entering the study The experience of using TENS or Acupuncture The use of oxytocin to induce and augmentation of labor before entering the study Mental and anatomical disorders (psychosis, schizophrenia, uterine abnormalities and pelvic stenosis) chronic diseases (heart disease, hypertension, diabetes) Skin diseases e (any lesion, inflammation and eczema) in the area of intervention high risk pregnancies (gestational hypertension, polyhydramnios and oligohydramnios known by ultrasound) Reduce fetal movements before entering the study Intrauterine growth retardation (IUGR) Rupture of membrane for more than 12 hours Use narcotics 12 hours before entering the study Infertility history

Design outcomes

Primary

MeasureTime frame
Pain severity score. Timepoint: 1. The beginning of the study, 2.One hour after the close of TENS 3.The beginning of the active phase (dilation of 4-5 cm) 4.The end of the first phase (full dilatation). Method of measurement: visual analogue scale (VAS).

Secondary

MeasureTime frame
TENS satisfaction score. Timepoint: 4 hours after childbirth. Method of measurement: Researcher made 3 questions questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Farjad Bastani

Guilan University of Medical Sciences

dr.farjadbastani@gmail.com+1 333369224

Outcome results

None listed

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