labor pain
Conditions
Interventions
Group 1:Routine nursing
Group 2:TENS
Group 3:Acupoint stimulation
Group 4:TENS combined acupoint stimulation
Sponsors
Obstetrics and Gynecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Pregnant women who have established a prenatal check-up in this institution and plan to give birth in this institution; 2. Single pregnancy, head position; 3. The mother and fetus are in good health when entering the room; 4. Willingness to undergo vaginal trial production; 5. Clear mind, no cognitive dysfunction and communication barriers; 6. Informed consent to participate in this study.
Exclusion criteria
Exclusion criteria: 1. There are serious complications before pregnancy or during pregnancy; 2. With medical indications for cesarean section.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Non-Pharmacological to pharmacological pain management Interval;Epidural analgesia rate;Delivery methods;Duration of the first, second and third stage of labor and total length of labor;Postpartumhemorrhag after 2 hours;First/fifth minutes Apgar score;Childbirth Experience;Perineal laceration; | — |
Countries
China
Contacts
Public ContactGu Chunyi
Obstetrics and Gynecology Hospital of Fudan University
Outcome results
None listed