Status:
COMPLETED
The Effect of Shower on Birth Pain, Postpartum Fatigue and Comfort
Lead Sponsor:
Kırklareli University
Conditions:
Pain
Fatigue
Eligibility:
FEMALE
20-35 years
Phase:
NA
Brief Summary
According to the definition of the International Association for the Study of Pain, pain; It is an unpleasant sensory and emotional sensation and behavior related to the individual's past experiences,...
Detailed Description
According to the definition of the International Association for the Study of Pain, pain; It is an unpleasant sensory and emotional sensation and behavior related to the individual's past experiences,...
Eligibility Criteria
Inclusion
- -Voluntarily agreeing to participate in the study
- She will have her second birth spontaneously vaginally at term (between 37-42 weeks of pregnancy).
- The fetal weight estimated by ultrasound is 2500-4000 grams
- Single fetus and head presentation
- Being in the active phase of labor (cervical dilation 4 cm)
- Ability to establish written/verbal communication
- Not taking any analgesia or anesthesia to relieve pain and fatigue before birth and during labor.
- Newborn APGAR score is 7 or above
Exclusion
- giving up on research
- Having received infertility treatment
- Birth by cesarean section
- Having an interventional birth (forceps, vacuum, episiotomy application)
- Being primiparous, having a third or more birth (grandmultiparous)
- Having any systemic, chronic and neurological disease (Diabetes Mellitus, Hypertension, Thyroid diseases, Multiple Sclerosis, Epilepsy, etc.)
- Regular use of medication due to any disease
- Receiving psychiatric treatment (pharmacotherapy/psychotherapy)
- Any induction application that will affect uterine contractions and dilation
- Having any pregnancy complications (placenta previa, preeclampsia, premature rupture of membranes, oligohydramnios and polyhydramnios, contraction anomalies, presentation disorder, intrauterine growth retardation, intrauterine dead fetus, macrosomic babies, fetal distress, etc.)
- Having any problem that prevents communication (such as not knowing Turkish, hearing, speaking and understanding impairment),
Key Trial Info
Start Date :
March 3 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 29 2024
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT06183957
Start Date
March 3 2023
End Date
February 29 2024
Last Update
June 6 2024
Active Locations (1)
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1
Tekirdağ Çorlu District State Hospital
Tekirdağ, Tekirdağ, Turkey (Türkiye)