← Back to Clinical Trials
Recruiting NCT06824337

Effect of Targeted Mobilization Program

Trial Parameters

Condition Caesarean Section
Sponsor Nigde Omer Halisdemir University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 64
Sex FEMALE
Min Age 18 Months
Max Age 35 Years
Start Date 2024-12-01
Completion 2025-03-01
Interventions
mobilization training and targeted mobilization

Brief Summary

This study was planned to evaluate the effect of early mobilization training given to patients undergoing cesarean section in the preoperative period and targeted mobilization program applied after the surgery, on preventing gastrointestinal complications that may develop after the surgical intervention and participating in breastfeeding and baby care. 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 at least a primary school graduate, who gave birth at term, who have a live singleton pregnancy, and who do not have a risky pregnancy history (DVT, thromboembolism) 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. Personal Information Form prepared in line with the literature, postoperative gastrointestinal functions information form, postoperative abdominal distension diagnosis form, walking chart, VAS, LATCH Breastfeeding Diagnosis and Evaluation Scale and Breastfeeding Information Form data collection forms 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

Eligibility 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

Related Trials