Impact of Video-Enhanced Consent on Informed Decision-Making for Parents of Extremely Preterm Infants Eligible for the ViDES Study

Understanding of Consent in Clinical Research Clinical Trial

Official title: Impact of Video-Enhanced Consent on Informed Decision-Making for Parents of Extremely Preterm Infants Eligible for the ViDES Study: A Randomized Controlled Trial

Status Not yet recruiting

Clinical Trial Summary

This pilot randomized controlled trial evaluates the impact of video-enhanced consent compared to the usual approach. The investigators aim to assess if video-enhanced consent empowers decision-making and improves understanding in parents considering participation in the ViDES study, which investigates the effectiveness of Vitamin D supplementation in extremely preterm infants (the ViDES study is separately registered as NCT05459298).

Clinical Trial Description

n/a

• NCT number: NCT06446492
• Study type: Interventional
• Source: The University of Texas Health Science Center, Houston
• Contact: Maria del Mar Romero López, MD, MS, PhD
• Phone: 713-500-7283
• Email: Maria.del.Mar.RomeroLopez@uth.tmc.edu
• Status: Not yet recruiting
• Phase: N/A
• Start date: July 1, 2024
• Completion date: December 31, 2025