Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: parturient women who are willing to participate Parturient women who are in active stage of labor Parturient Women with normal course of pregnancy
Exclusion criteria
Exclusion criteria: Parturient women with current bed sore in lumbo-sacral region Parturient women who underwent spinal surgeries Parturient women with administration of analgesic drug
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| There will be significant difference in intensity of labor pain among experimental group & control groupTimepoint: after 20 minute,50 minute & 80 minute of intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| There will be significant association between selected clinical variable and intensity of labor painTimepoint: After 20 minute,50 minute & 80 minute of intervention | — |
Countries
India
Contacts
All India Institute of Medical Sciences,Bhopal