Status:
UNKNOWN
The Effect of Paula Method Exercises on Post-cesarean Section Distension
Lead Sponsor:
Akdeniz University
Conditions:
Cesarean Section Complications
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief Summary
Aim:To examine the effect of "Paula Method Exercises" after cesarean section on the prevention of postoperative distention and pain due to distension. Method: The study was planned as a double-blind,...
Detailed Description
Aim:To examine the effect of "Paula Method Exercises" after cesarean section on the prevention of postoperative distention and pain due to distension. The gastrointestinal system problems experienced ...
Eligibility Criteria
Inclusion
- Between the ages of 18-45, who are planned to have an elective Cesarean Section (CD) under spinal anesthesia,
- Admitted to the service within six hours after cesarean section,
- No chronic Charles Bonnet Syndrome (CBS) disease,
- No history of serious (ilostomy, cholastomy, irritable bowel syndrome, etc.) disease related to the gastrointestinal tract,
- Those who volunteered to participate in the study and whose consent was obtained,
- No complications developed during or after the surgery,
- Women who do not have intellectual disability or perception problems and do not have communication difficulties will be included in the study.
- In order not to affect the research results; If there are women in the intervention and control group in the same hospital room, the last woman who was hospitalized in the same room will be excluded from the study.
Exclusion
- Enema made,
- Any complication developed and taken to the intensive care unit,
- Not complying with the application process,
- The state of consciousness is not clear / will not be able to participate in the applications,
- Women who cannot communicate for any reason (hearing/speech/hearing, etc.) will be excluded from the research.
- Discharged before two days after cesarean section
Key Trial Info
Start Date :
November 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 30 2022
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT05283707
Start Date
November 1 2021
End Date
December 30 2022
Last Update
March 17 2022
Active Locations (1)
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1
Akdeniz Univercity
Antalya, Konyaaltı, Turkey (Türkiye), 07058