Comprehension of Research Informed Consent When Applied Through a Telemedicine Medium

PHASE2CompletedINTERVENTIONAL
Enrollment

130

Participants

Timeline

Start Date

June 30, 2015

Primary Completion Date

September 30, 2015

Study Completion Date

September 30, 2015

Conditions
Informed Consent
Interventions
PROCEDURE

Audio-visual telemedicine

Participants in an emergency department will have their care delivered using telemedicine, then they will be approached for a study by a study investigator using the same telemedicine link

PROCEDURE

Standard care

Participants in an emergency department will have their care delivered in person, then they will be approached by a study investigator face-to-face.

Trial Locations (1)

52242

University of Iowa Hospitals and Clinics, Iowa City

All Listed Sponsors
lead

University of Iowa

OTHER

NCT02541799 - Comprehension of Research Informed Consent When Applied Through a Telemedicine Medium | Biotech Hunter | Biotech Hunter