Actively Recruiting
Information and Progressive Relaxation Exercises
Led by Nigde Omer Halisdemir University · Updated on 2024-11-27
68
Participants Needed
1
Research Sites
27 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study was planned to determine the effect of information and progressive relaxation exercises before planned cesarean section on surgical fear, anxiety, postpartum comfort and pain levels.The research will be conducted in experimental design. The research will begin after receiving written permission from Niğde Ömer Halisdemir University Ethics Committee, Niğde Provincial Health Directorate and Ömer Halisdemir Training and Research Hospital. Pregnant women who are between the ages of 18-35, who are on Primigravida, who apply for a planned cesarean section, who have a live single pregnancy, and who are planned for spinal anesthesia will be included in the study. Before starting the research, the study will begin by obtaining institutional permissions and written permission from the pregnant women. Pre-Assessment Form, Personal Information Form, State Anxiety Scale, Surgical Fear Scale, Postpartum Comfort Scale will be used to collect data. The data will be evaluated on a computer using the IBM SPSS Statistics 24 (Statistical Package for the Social Sciences for Windows) package program. Appropriate statistical analyzes will be used to evaluate the data.
CONDITIONS
Official Title
Information and Progressive Relaxation Exercises
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between the ages of 18-35
- Primigravida (first pregnancy)
- Scheduled for planned cesarean section
- Live singleton pregnancy
- Spinal anesthesia planned for surgery
You will not qualify if you...
- Development of postpartum maternal or newborn complications
- Receiving general anesthesia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ömer Halisdemir University Training and Research Hospital
Niğde, Turkey (Türkiye)
Actively Recruiting
Research Team
B
BİRNUR YEŞİLDAĞ, Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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