Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02885532 · ClinicalTrials.gov registry record
Capacity to Consent in Acutely Intoxicated Emergency Department Patients
A clinical trial of Informed Consent, sponsored by Hennepin Healthcare Research Institute.
- Completed
- Registry status
- 417
- Enrollment target
- 1
- Study location
NCT02885532 is a study of Informed Consent that has completed, run by Hennepin Healthcare Research Institute. The registered enrollment target is 417 participants, below the 871-participant average among 9 other Informed Consent trials with a reported enrollment target (52% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02885532, a study of Informed Consent, has completed, sponsored by Hennepin Healthcare Research Institute.
- COMPLETED
- Registry status
- 417 participants
- Enrollment target
- 1
- Study location
Study Summary
The ability to meaningfully consent intoxicated and chemically dependent patients for research has inhibited medical advances in this vulnerable population. A recent pilot supported use of the University of California, San Diego Brief Assessment of Capacity to Consent tool to assess the capacity of intoxicated emergency department patients to participate in research. The objective is to determine the number of intoxicated emergency department patients who could correctly complete the questionnaire, and evaluate alcohol concentration, sedation and ability to recall participation upon sobriety.
Conditions Studied
Interventions
- OTHER University of California, San Diego Brief Assessment of Capacity to Consent Tool
Study Locations (1)
Minnesota
- Hennepin County Medical Center - Minneapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 417 participants |
| Start Date | 2015-07 |
| Est. Completion | 2016-03 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02885532
The ClinicalTrials.gov registry entry for NCT02885532 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 417 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 871-participant average among 9 other Informed Consent trials with a reported enrollment target (52% lower). The listed sponsor is Hennepin Healthcare Research Institute, which has 63 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Informed Consent appearing as the primary indexed condition, and to 1 intervention - of which University of California, San Diego Brief Assessment of Capacity to Consent Tool is the first listed.
NCT02885532 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.
Frequently Asked Questions
What is clinical trial NCT02885532 about?
NCT02885532 is a clinical study titled "Capacity to Consent in Acutely Intoxicated Emergency Department Patients". The ability to meaningfully consent intoxicated and chemically dependent patients for research has inhibited medical advances in this vulnerable population. A recent pilot supported use of the University of California, San Diego Brief Assessment of Capacity to Consent tool to assess the capacity of ...
What is the current status of trial NCT02885532?
This trial is currently completed. The enrollment target is 417 participants. The study started on 2015-07. Estimated completion is 2016-03.
What conditions does trial NCT02885532 study?
This clinical trial studies the following conditions: Informed Consent.
What interventions are being tested in trial NCT02885532?
The interventions under investigation include: University of California, San Diego Brief Assessment of Capacity to Consent Tool (OTHER).
Who is sponsoring clinical trial NCT02885532?
This trial is sponsored by Hennepin Healthcare Research Institute, which has 63 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02885532 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Informed Consent
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
AI-Driven Consent Simplification Study
RECRUITING
-
Implementing a Novel Consent Process for Biospecimen Research After Newborn Screening
RECRUITING · NA
-
Optimizing Timing of Cesarean Delivery Consent on Labor and Delivery
RECRUITING · NA
-
Video-Assisted Informed Consent for Neonatal Lumbar Puncture
ACTIVE NOT RECRUITING · NA
-
GEM: Impact of a Video Education Tool on Decisional Conflict Among Prenatal Patients
ACTIVE NOT RECRUITING · NA
-
The New Executive and Appendix Template (NEAT) Study
COMPLETED · NA
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.