Actively Recruiting
Effect of Targeted Mobilization Program Applied After Caesarean Section Surgery on Care Outcomes: Randomized Controlled Study
Led by Nigde Omer Halisdemir University · Updated on 2025-02-13
64
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effect of early mobilization training given before cesarean section surgery and a targeted mobilization program applied after surgery. The study aims to see if these interventions can prevent gastrointestinal complications after cesarean delivery and help with breastfeeding and baby care. Increasing cesarean section rates worldwide have made postoperative care more important, but the best way to implement early mobilization is still unclear. This study uses an experimental design to fill this knowledge gap and improve recovery outcomes for mothers. The study includes two groups: an intervention group receiving early mobilization education before surgery and a targeted mobilization program afterward, and a control group receiving routine care. The intervention group learns about the benefits of early mobilization, step goals, and how to use a smartphone pedometer and diary to track walking time and steps. The control group will record their walking distance as part of routine care. The study is randomized and open-label, starting with patient education at hospital admission. Participants will complete forms including postoperative gastrointestinal function, abdominal distension diagnosis, pain assessment using a visual analog scale, breastfeeding evaluation using the LATCH scale, and other breastfeeding information. Data collection occurs over three months. Researchers will analyze these outcomes to assess the impact of the mobilization program on recovery, breastfeeding participation, and gastrointestinal health after cesarean section. The study is sponsored by Nigde Omer Halisdemir University and runs until April 2025.
CONDITIONS
Brief Title
Effect of Targeted Mobilization Program
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between the ages of 18-35
- At least primary school graduate
- Giving birth at term
- Having a live singleton pregnancy
- No risky pregnancy history (DVT, thromboembolism)
- Women who can use a mobile phone
You will not qualify if you...
- Those who want to leave the study
- Undergoing emergency caesarean section
- Not recording walking distance
- Women who cannot be interviewed within 24 hours of discharge
- Women who develop maternal or neonatal complications after birth
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) to provide informed consent and initial assessment
Duration - From the day of surgery through hospital stay until discharge
Participants receive early mobilization training before cesarean section and follow a targeted mobilization program after surgery to support recovery and prevent complications.
Daily mobilization activities and monitoring during hospital stay
Duration - Up to 3 months after surgery
Participants are monitored for postoperative gastrointestinal function, breastfeeding success, and overall recovery for up to 3 months after surgery.
Assessments conducted during routine follow-up visits over 3 months
Trial Site Locations
Total: 1 location
1
Niğde Ömer Halisdemir Univercity
Niğde, Turkey (Türkiye)
Actively Recruiting
Research Team
B
BİRNUR YEŞİLDAĞ, DR.
B
birnur yeşildağ, dr
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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