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NCT06256822

Technology-Based Breastfeeding Training After Cesarean

Completed Last updated 13 February 2024
What this trial tests

trial in Cesarean Section; Dehiscence in 66 participants. Completed in 1 October 2023.

Timeline
1 January 2023
Primary endpoint
1 September 2023
1 October 2023

Quick facts

Lead sponsorOrdu University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment66
Start date1 January 2023
Primary completion1 September 2023
Estimated completion1 October 2023
Sites1 location across Turkey (Türkiye)

Conditions studied

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:

Other recruiting trials for Cesarean Section; Dehiscence

Currently open trials in the same condition.

Other Ordu University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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