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Improving Consent and Survey Procedures for Young MSM in Web-based HIV Prevention

NCT02139566 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2405

Last updated 2016-01-15

No results posted yet for this study

Summary

A two-part study to test the efficacy of alternative consent procedures and the efficacy of alternative methods to improve survey completion.

Conditions

  • Healthy

Interventions

BEHAVIORAL

Video consent (high-tech)

Consent provided by an animated video with captions

BEHAVIORAL

Video consent (low-tech)

This consent is a video production of the informed consent information, taped using a staff member with basic video equipment.

BEHAVIORAL

FAQ format consent

This consent modality will present the basic information from the informed consent in an interactive, "frequently asked questions" format. Upon clicking each question, the participant will be shown a short text response to that question.

BEHAVIORAL

Standard consent

The standard consent form will present the full informed consent document in a scrolling text window within the browser window. Participants will be asked to review the document online.

BEHAVIORAL

PDF informed consent document

A PDF of the full consent document will be available for download, through hyperlink on the consent page. This is provided for video (low-tech), video (high-tech), FAQ format, and standard informed consent.

Sponsors & Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH

  • Emory University

    lead OTHER

Principal Investigators

  • Patrick S Sullivan, PhD · Emory University

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
34 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2015-05-31
Completion
2015-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02139566 on ClinicalTrials.gov