Non-Pharmacological Method to Relieve Back Pain
Pain
About this trial
This is an interventional supportive care trial for Pain focused on measuring Back Pain, Late postpartum, Cesarean Section
Eligibility Criteria
Inclusion Criteria: 18-49 years old, Able to read and write Turkish Postpartum 1st week and within 4th week Primiparous and multiparous Those who had a registered cesarean section in the family health center where the study was conducted, Able to speak and understand Turkish, Back pain score above 4 according to VAS (Visual analog scale), Participants who voluntarily agree to participate in the study will be included in the study. Exclusion Criteria: Congenital anomaly in the baby who gave a stillbirth, whose baby is hospitalized in the neonatal intensive care unit, Use of cigarettes or alcohol History of past or present mental illness, Using antidepressants or anxiolytic drugs, With rheumatoid arthritis, ankylosing spondylitis, Scheuermann's disease, Ehlers-Danlos syndrome, spinal surgeries, nerve root compression, spondylolisthesis comorbid disease, Perineal edema, hematoma, wound dehiscence, bladder catheterization and serious postpartum complications (internal bleeding, femoral artery embolism, pelvic fracture), With impaired tissue integrity in the area to be applied, Vaginal delivery, Taking painkillers in the last 6 hours, In addition, those who want to leave the research at any stage of the research will be excluded from the research.
Sites / Locations
- Kocaeli UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Acupressure group
Control group
Participants in this group will be interviewed for the first time in the first week of postpartum and for the second time in the fourth week of postpartum. The application will be explained and a voluntary consent form will be signed. Participant Information Form will be filled in by the researcher by face-to-face interview. The VAS that will be applied to the participant to evaluate the back pain just before the application will be filled in by the participant. The VAS Evaluating Back Pain after the application will be filled in by the participant. The participant will be informed that the study has been completed.
Participants in this group will be interviewed for the first time in the first week of postpartum and for the second time in the fourth week of postpartum. The application will be explained and a voluntary consent form will be signed. Participant Information Form will be filled in by the researcher by face-to-face interview. VAS to assess back pain will be filled in by the participant. No application will be made to this group.