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

NACompletedINTERVENTIONAL
Enrollment

83

Participants

Timeline

Start Date

July 1, 2024

Primary Completion Date

June 15, 2025

Study Completion Date

June 15, 2025

Conditions
Understanding of Consent in Clinical ResearchImplementation of Video-Consent in Clinical Research
Interventions
OTHER

ViDEO explaining study

The research team will introduce themselves and ask the parents to watch an informational video explaining the ViDES study on an iPad while they stay in the room with the parents. After viewing the video, the team will answer any questions and provide written consent and enough time to decide whether to participate in the study. The research team will also provide a QR code that grants parents/guardians access to the video on their own device at any time. This allows them to pause, rewind, and revisit the information.

OTHER

Usual Care

The research team will present a detailed explanation of the ViDES study, answer questions, provide written consent, and provide enough time to decide on participation or not in the study.

Trial Locations (1)

77030

McGovern Medical School at UTHealth Houston, Houston

All Listed Sponsors
lead

The University of Texas Health Science Center, Houston

OTHER

NCT06446492 - Impact of Video-Enhanced Consent on Informed Decision-Making for Parents of Extremely Preterm Infants Eligible for the ViDES Study | Biotech Hunter | Biotech Hunter