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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ViDES trial consent rate
Timeframe: Within 1 week of the intervention
Participants' understanding of the ViDES study as assessed by a questionnaire
Timeframe: Within 48 hours of the intervention
Participants' satisfaction with consent approach as assessed by a questionnaire
Timeframe: Within 48 hours of the intervention
Participant's opinions related to participation in research as assessed by a questionnaire
Timeframe: Within 48 hours of the intervention