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Acupressure Applied After Cesarean Section on Postpartum Pain

E

Eastern Mediterranean University

Status

Completed

Conditions

Cesarean Section Complications
Postpartum Disorder

Treatments

Behavioral: acupressure

Study type

Observational

Funder types

Other

Identifiers

NCT06138288
ETK00-2023-0107

Details and patient eligibility

About

Pressure applied according to the principles of acupressure limits the pain limit, reduces the secretion of endorphins, which is a neurochemical, reduces the tension in the muscles, reduces the amount of oxygen in the blood flow, and finally provides duration and relaxation. Acupressure application is becoming more and more common nowadays because it is a noninvasive, safe, easy-to-apply and effective method without side effects. It seems that there is a limit to the study in which group acupressure applications in the literature are examined together on pain and comfort after cesarean section. In these basic points, the expectations of achieving postpartum pain and postpartum comfort of acupressure applied after cesarean delivery in this study. The circle of the research; There will be women who will have repeated cesarean section in a private Obstetrics Clinic in Famagusta. Women will be separated from two groups, one group will continue acupressure and the other group will do routine care. Visual analog scale and end-of-birth comfort procedure will be applied to women before and after the application.

Full description

Pressure applied according to the principles of acupressure limits the pain limit, reduces the secretion of endorphins, which is a neurochemical, reduces the tension in the muscles, reduces the amount of oxygen in the blood flow, and finally provides duration and relaxation. Acupressure application is becoming more and more common nowadays because it is a noninvasive, safe, easy-to-apply and effective method without side effects. It seems that there is a limit to the study in which group acupressure applications in the literature are examined together on pain and comfort after cesarean section. In these basic points, the expectations of achieving postpartum pain and postpartum comfort of acupressure applied after cesarean delivery in this study. The circle of the research; There will be women who will have repeated cesarean section in a private Obstetrics Clinic in Famagusta. Women will be separated from two groups, one group will continue acupressure and the other group will do routine care. Visual analog scale and end-of-birth comfort procedure will be applied to women before and after the application.

Enrollment

60 patients

Sex

Female

Ages

18 to 49 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • agreeing to participate in the research,
  • be between the ages of 18-49,
  • To give birth by cesarean section between 37-40 weeks,
  • Having a healthy and live birth at the end of a single pregnancy,
  • Receiving spinal anesthesia
  • Being able to read and write Turkish and be open to communication.

Exclusion criteria

  • Absence of pain in the 2nd hour postpartum
  • Having a cesarean delivery after a risky pregnancy,
  • Having a chronic illness
  • Having severe systemic disease
  • Not receiving spinal anesthesia
  • Having a body mass index over 25,
  • Have previous acupressure experience.

Trial design

60 participants in 2 patient groups

acupressure group
Description:
Women who are in acupressure will apply the application after cesarean section 2nd hour after applying the data collection forms (descriptive features formula, VAS, WHO). For women on acupressure, the application will be applied manually to the SP6, P6 and L14 points in the order indicated by the drawing with the index or middle finger, 1-1.5 cm depth for 5 seconds, pressing for 5 seconds, resting for 2 seconds and continuing for 2 minutes to go. will be with you. VAS will be filled again after the application.
Treatment:
Behavioral: acupressure
control group

Trial contacts and locations

1

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Central trial contact

Hilal Begum Cayır, Research Assistant

Data sourced from clinicaltrials.gov

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