labor pain in active parturition phase. delivery(single)normal
Conditions
Interventions
Intervention 1: Trial group: used the Tens on back (L1-T10). Intervention 2: Tens plasebo group: group received no electrical stimulation. Intervention 3: control group: no Intervention.
Treatment - Other
Placebo
Trial group: used the Tens on back (L1-T10)
Tens plasebo group: group received no electrical stimulation
control group: no Intervention
Sponsors
Golestan University Of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: inclusion criteria: primiparous? term pregnancy?cephalic presentaition?at active phase of the first stage of labor with cervical dilataion3-5 cm; age between 20-40 years- exclusion criteria: maternal cutaneous on the application site such as wound scar; pacemaker user
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Labor pain in active phase. Timepoint: Measurement of pain,right after intervention,30minutes,60minutes after intervention. Method of measurement: visual analogue scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMersedeh Kia
Golestan University Of Medical Sciences
Outcome results
None listed