Status:
COMPLETED
Nonpharmacological Method and Postpartum Fatigue
Lead Sponsor:
resmiye kaya odabaş
Conditions:
Fatigue
Eligibility:
FEMALE
18-35 years
Phase:
NA
Brief Summary
Postpartum fatigue is common in women after cesarean section and it affects the woman and the baby. Many noninvasive applications help to overcome this problem. This study was planned as a randomized ...
Detailed Description
Aim: The aim of this study is to determine the effect of acupressure on postpartum fatigue in women who had cesarean section. Hypotheses: H0: There is no difference in fatigue between the acupressur...
Eligibility Criteria
Inclusion
- Between the ages of 18-35,
- Birth after 36th gestational week,
- Multiparous
- Caesarean section with regional anesthesia,
- Mobilized,
- Not having any health problems (Hypertension, tuberculosis, HIV, cancer, psychological disorders, etc.),
- Does not have any problems preventing communication,
- At least primary school graduate,
- Able to speak and understand Turkish,
- Volunteer women who agreed to participate in the study
Exclusion
- Having postpartum complications (bleeding, embolism, eclampsia, infection, etc.),
- Having a hemoglobin level of less than 9 g/dl and a hematocrit level of less than 30%,
- Having a body mass index of 40 and above,
- Covid-19 test positive,
- Having twin babies,
- The baby is in the neonatal intensive care unit,
- Having been diagnosed psychologically (such as depression) before,
- Women who do not want to participate in the research will be excluded from the study.
Key Trial Info
Start Date :
August 12 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 13 2022
Estimated Enrollment :
122 Patients enrolled
Trial Details
Trial ID
NCT05201157
Start Date
August 12 2021
End Date
March 13 2022
Last Update
April 26 2022
Active Locations (1)
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1
Aydın Adnan Menderes University
Efeler, Aydın, Turkey (Türkiye), 09010