None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Primigravid women aged 18 years and above willing to participate in the study At term (37–42 weeks of gestation age) Primigravid women with no complications during the antenatal period Established active stage of labor A single viable fetus in cephalic presentation Intact ovular membranes The ability to read the consent form and understand the study.
Exclusion criteria
Exclusion criteria: Preterm labor Malpresentation Cephalopelvic disproportion Antepartum hemorrhage Any medical complications Known fetal abnormalities Multigravid women Women in the advanced stage of labor Psychiatric disorders Skin lesions on the electrode application site Presence of pacemaker
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Evaluation of pain intensity during labor using visual analog scale 2. Measure of womens satisfaction with care and the experience of labor and birth using the Birth Satisfaction Scale-Revised (BSS-R)Timepoint: 1. Baseline - before starting the intervention Post-intervention - after 30 minutes of intervention 2. 24-48 hours post-delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Duration of first stage of labor using partograph 2. Neonatal outcome - APGAR score at 5 minTimepoint: Post-delivery | — |
Countries
India
Contacts
Mother Theresa Post Graduate and Research Institue of Health Sciences