Effect of early mobilization on recovery after cesarean section
Effect of Targeted Mobilization Program Applied After Caesarean Section Surgery on Care Outcomes: Randomized Controlled Study
NA · Nigde Omer Halisdemir University · NCT06824337
This study tests if a special movement program before and after cesarean sections can help new moms recover better and take care of their babies.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 64 (estimated) |
| Ages | 18 Months to 35 Years |
| Sex | Female |
| Sponsor | Nigde Omer Halisdemir University (other) |
| Locations | 1 site (Niğde) |
| Trial ID | NCT06824337 on ClinicalTrials.gov |
What this trial studies
This study evaluates the impact of a targeted mobilization program on women undergoing cesarean sections. It focuses on early mobilization training before surgery and specific mobilization techniques applied postoperatively to prevent gastrointestinal complications and enhance participation in breastfeeding and baby care. The research is designed as an experimental study and will be conducted after obtaining necessary ethical approvals. Participants will be monitored for their recovery and ability to engage in infant care following the intervention.
Who should consider this trial
Good fit: Ideal candidates are pregnant women aged 18-35 with a live singleton pregnancy and no history of risky pregnancy complications.
Not a fit: Patients who undergo emergency cesarean sections or develop complications after birth may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve recovery outcomes for women after cesarean sections, facilitating better breastfeeding and infant care.
How similar studies have performed: Other studies have shown positive outcomes with early mobilization techniques in postoperative recovery, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * Exclusion Criteria for the Study * 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
Where this trial is running
Niğde
- Niğde Ömer Halisdemir Univercity — Niğde, Turkey (Türkiye) (RECRUITING)
Study contacts
- Principal investigator: isa temur, Dr — NİĞDE ÖMER HALİSDEMİR UNIVERCITY
- Study coordinator: BİRNUR YEŞİLDAĞ, DR.
- Email: nurumbirnur@gmail.com
- Phone: +90 05336815923
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Caesarean Section, Mobility, Pain, Breastfeeding, Caesarean section, mobilization, pain, breastfeeding