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NCT06446492 · ClinicalTrials.gov registry record · NA
Impact of Video-Enhanced Consent on Informed Decision-Making for Parents of Extremely Preterm Infants Eligible for the ViDES Study
A NA study of Understanding of Consent in Clinical Research and Implementation of Video-Consent in Clinical Research, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- NA
- Development phase
- 83
- Enrollment target
- 1
- Study location
NCT06446492 is a NA study of Understanding of Consent in Clinical Research and Implementation of Video-Consent in Clinical Research that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 83 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06446492, a NA study of Understanding of Consent in Clinical Research and Implementation of Video-Consent in Clinical Research, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- NA
- Development phase
- 83 participants
- Enrollment target
- 1
- Study location
Study 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).
Conditions Studied
Interventions
- OTHER Usual Care
- OTHER ViDEO explaining study
Study Locations (1)
Texas
- McGovern Medical School at UTHealth Houston - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 83 participants |
| Start Date | 2024-07-01 |
| Est. Completion | 2025-06-15 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06446492
The ClinicalTrials.gov registry entry for NCT06446492 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 83 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Understanding of Consent in Clinical Research appearing as the primary indexed condition, and to 2 interventions - of which Usual Care is the first listed.
NCT06446492 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT06446492 about?
NCT06446492 is a clinical study titled "Impact of Video-Enhanced Consent on Informed Decision-Making for Parents of Extremely Preterm Infants Eligible for the ViDES Study". 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 investiga...
What is the current status of trial NCT06446492?
This trial is currently completed. It is a NA study. The enrollment target is 83 participants. The study started on 2024-07-01. Estimated completion is 2025-06-15.
What conditions does trial NCT06446492 study?
This clinical trial studies the following conditions: Understanding of Consent in Clinical Research, Implementation of Video-Consent in Clinical Research.
What interventions are being tested in trial NCT06446492?
The interventions under investigation include: Usual Care (OTHER), ViDEO explaining study (OTHER).
Who is sponsoring clinical trial NCT06446492?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06446492 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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