Effect of Targeted Mobilization Program

Recruiting now · Not applicable

Conditions studied: Caesarean Section, Mobility, Pain, Breastfeeding

In brief

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

Key facts

Study ID: NCT06824337
Run by: Nigde Omer Halisdemir University
People needed: 64
Starts: 2024-12-01
Expected to finish: 2025-04-01
Last updated by the study team: 2025-02-13

Who can join

Age: 2 and older, up to 35. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

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 may not qualify if…

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 it is running

Niğde Ömer Halisdemir Univercity — Niğde, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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