Clinical Trial: Impact of Video-Enhanced Consent on Informed Decision-Making for Parents of Extremely Preterm Infants Eligible for the ViDES Study
Study Status: COMPLETED
Recruit Status: COMPLETED
Condition: Understanding of Consent in Clinical Research
Study Type: INTERVENTIONAL
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
Brief 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).
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