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Showing 1–4 of 4 matching trials from the live ClinicalTrials.gov search.
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Filters: Condition: Parental Consent Clear all
Completed No phase listed Observational Accepts healthy volunteers

Effectiveness of the Consent Process

NCT00630136
View directory record Official record
Conditions
Parental Consent
Interventions
interview
Behavioral
Lead sponsor
Children's Mercy Hospital Kansas City
Other
Eligibility
18 Years and older
Enrollment
20 participants
Healthy volunteers
Accepts healthy volunteers
Timeline
2008
U.S. locations
1
States / cities
Kansas City, Missouri
Source: ClinicalTrials.gov public record
Updated Mar 23, 2010 · Synced Jul 24, 2026, 1:10 AM EDT
Completed No phase listed Observational

Parental Permission and Adolescent Assent and Decision-Making in Clinical Research

NCT00571311
View directory record Official record
Conditions
Adolescents
Interventions
Not listed
Lead sponsor
National Institutes of Health Clinical Center (CC)
NIH
Eligibility
13 Years to 18 Years
Enrollment
356 participants
Healthy volunteers
Healthy volunteers not accepted
Timeline
2007 – 2018
U.S. locations
1
States / cities
Bethesda, Maryland
Source: ClinicalTrials.gov public record
Updated Oct 8, 2019 · Synced Jul 24, 2026, 1:10 AM EDT
Completed Not applicable Interventional Accepts healthy volunteers

Facilitating Learning Health Care (LHC) and Neonatal Research: Effects of a Brief Introductory Discussion Between a Neonatologist and the Parents of Eligible Infants

NCT05541536
View directory record Official record
Conditions
Understanding of Consent in Clinical Research, Implementation of Consent in Clinical Research
Interventions
Consultation meeting, Pamphlet, Usual Care
Other
Lead sponsor
The University of Texas Health Science Center, Houston
Other
Eligibility
Female only
Enrollment
100 participants
Healthy volunteers
Accepts healthy volunteers
Timeline
2022 – 2023
U.S. locations
1
States / cities
Houston, Texas
Source: ClinicalTrials.gov public record
Updated Dec 14, 2023 · Synced Jul 24, 2026, 1:10 AM EDT
Completed Not applicable Interventional Accepts healthy volunteers

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

NCT06446492
View directory record Official record
Conditions
Understanding of Consent in Clinical Research, Implementation of Video-Consent in Clinical Research
Interventions
ViDEO explaining study, Usual Care
Other
Lead sponsor
The University of Texas Health Science Center, Houston
Other
Eligibility
Not listed
Enrollment
83 participants
Healthy volunteers
Accepts healthy volunteers
Timeline
2024 – 2025
U.S. locations
1
States / cities
Houston, Texas
Source: ClinicalTrials.gov public record
Updated Jun 25, 2025 · Synced Jul 24, 2026, 1:10 AM EDT