Nonpharmacological Method for Relief of Uterine Pain

NACompletedINTERVENTIONAL
Enrollment

122

Participants

Timeline

Start Date

June 16, 2022

Primary Completion Date

August 26, 2022

Study Completion Date

November 24, 2022

Conditions
Pain
Interventions
BEHAVIORAL

Acupressure group

A suitable environment will be prepared for mothers in terms of warmth and light, where privacy can be protected. The application points will be determined with the acu-point device by choosing the most comfortable position of the mother, leaving the application points open. The most preferred points LI4 and SP6 were selected among the points that were reported to be effective in relieving luterus pain by scanning the literature on the points to be compressed. Acupressure will be applied to the points (bidirectional, right and left) for 2 minutes, for a total of 8 minutes. Light pressure will be applied with the thumb of the practitioner's hand. Immediately after applying pressure for 2 minutes for each point, it is passed to the other point in the symmetrical region and the application is made without interruption. While practicing, the researcher will check the time using a digital wristwatch with a stopwatch.

OTHER

Control group

No application will be made. The mothers in this group will fill in the visual analog scale, which evaluates postpartum uterine pain 3 times between 6-24 hours after birth.

Trial Locations (1)

41380

Kocaeli University, Kocaeli

All Listed Sponsors
collaborator

Medipol University

OTHER

lead

Kocaeli University

OTHER