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NCT06256822
Technology-Based Breastfeeding Training After Cesarean
trial in Cesarean Section; Dehiscence in 66 participants. Completed in 1 October 2023.
1 September 2023
Quick facts
| Lead sponsor | Ordu University |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 66 |
| Start date | 1 January 2023 |
| Primary completion | 1 September 2023 |
| Estimated completion | 1 October 2023 |
| Sites | 1 location across Turkey (Türkiye) |
Conditions studied
- Cesarean Section; Dehiscence — all drugs for Cesarean Section; Dehiscence →
- Breast Feeding — all drugs for Breast Feeding →
- Self Efficacy — all drugs for Self Efficacy →
Sponsor
Ordu University
Who can join
Adults 18 to 49, female only, with Cesarean Section; Dehiscence or Breast Feeding. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Aim: The aim of this study was to determine the effect of breastfeeding training given with virtual reality (VR) to postpartum primiparous mothers on breastfeeding success and breastfeeding self-efficacy. Method: The research was designed as a prospective randomized controlled study. In total, 66 women were included in the study, with 31 in the control group and 35 in the intervention group. The intervention group watched a breastfeeding video with VR in the 4th and 24th hours after cesarean. Research data were collected with the sociodemographic information form, LATCH Breastfeeding Charting System and Documentation Tool and the Breastfeeding Self-Efficacy Scale. The study included mothers who gave birth with cesarean section, received breastfeeding counseling during pregnancy, with no vision or hearing disabilities and without any neurological disorder.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06256822
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Related trials
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Other Ordu University trials
Trials by the same sponsor.
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- NCT07517549 — Sexual Health Education During Pregnancy · NA · recruiting
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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 NCT06256822 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Ordu University
- Last refreshed: 13 February 2024
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/NCT06256822.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing