Actively Recruiting

Phase Not Applicable
Age: 18Months - 35Years
FEMALE
ID06824337

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

Age: 18Months - 35Years
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

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

Treatment

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

Follow-up

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

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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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