Women undergoing cesarean section. Delivery by emergency caesarean section
Conditions
Interventions
Intervention 1: The intervention group 1- Acupuncture at Hugo Point (LI4): These subjects, after being fully conscious while lying back, The researcher will use the thumb of both her hands at the Hugo
Treatment - Other
The intervention group 1- Acupuncture at Hugo Point (LI4): These subjects, after being fully conscious while lying back, The researcher will use the thumb of both her hands at the Hugo Point on either
Intervention group: 2- Acupressure at the Saninjao Point (SP6): These subjects, after being fully conscious and returning the sensation of lower limbs while lying back, The researcher will be placed
Control group: After the consciousness and the return of sensation in the lower limbs of these subjects, while lying behind, the researcher will be placed face- to face to them, and in half of them at
Sponsors
Rafsanjan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Term pregnancy 2. No previous experience of acupressure 3. Having ages 45-18 years 4. Lack of a lesion at the site of the practice of pressure or touch 5. No addiction 6. Failure to have speech and hearing ability 7. Not having known psychiatric disorders 8. Not having crises such as divorce, loss of loved ones, immigration or .... over the past 6 months 9. Elective cesarean section Exit criteria: 1-Unwillingness to cooperate with each of the research units during the study 2. Those with acute complications after cesarean section (severe bleeding, embolism, etc.) 3- Those who during the intervention until the second assessment of the severity of pain will necessarily need to receive the housing
Exclusion criteria
Exclusion criteria: Exit criteria:2. Those with acute complications after cesarean section (severe bleeding, embolism, etc.)3- Those who during the intervention until the second assessment of the severity of pain will necessarily need to receive the housing
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post ceaerian section. Timepoint: Immediately and hour after study. Method of measurement: for vas scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMarzeyeloripoor
Rafsanjan University of Medical Sciences
Outcome results
None listed