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NCT06824337: Mobilization
Effect of Targeted Mobilization Program
NA trial testing mobilization training and targeted mobilization in Caesarean Section in 64 participants. Currently enrolling.
1 March 2025
Quick facts
| Lead sponsor | Nigde Omer Halisdemir University |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 64 |
| Start date | 1 December 2024 |
| Primary completion | 1 March 2025 |
| Estimated completion | 1 April 2025 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- mobilization training and targeted mobilization
Conditions studied
- Caesarean Section — all drugs for Caesarean Section →
- Mobility — all drugs for Mobility →
- Pain — all drugs for Pain →
- Breastfeeding — all drugs for Breastfeeding →
Sponsor
Nigde Omer Halisdemir University
Who can join
Adults 18 Months to 35, female only, with Caesarean Section or Mobility. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
The effect of a targeted mobilization program applied after cesarean surgery on care outcomes: a randomized controlled study.
Yesildag B, Atmaca KA, Temur I. · · 2026 · PMID 42138935 · DOI 10.1590/1806-9282.20251440
Verify or expand the search:
- PubMed search for NCT06824337
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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Other Nigde Omer Halisdemir University trials
Trials by the same sponsor.
- NCT07392619 — The Effect of Acupressure on Symptoms in Elderly Adults With Painful Diabetic Neuropathy · NA · not yet recruiting
- NCT07525726 — The Relationship Between Finger Ratio and Development in Infants · enrolling by invitation
- NCT07468981 — Movement Quality and Mechanical Properties of the Muscle · active not recruiting
- NCT07440667 — Restrictive vs Liberal Intraoperative Fluid Strategy and Postoperative Outcomes After Elective Cesarean Section · NA · recruiting
- NCT07409337 — Self-Acupressure for Primary Dysmenorrhea and Premenstrual Symptoms · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06824337 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Nigde Omer Halisdemir University
- Last refreshed: 13 February 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06824337.
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