Increasing HIV Testing in Urban Emergency Departments Via Mobile Technology

Sponsor
National Development and Research Institutes, Inc. (Other)
Overall Status
Unknown status
CT.gov ID
NCT02154802
Collaborator
(none)
300
1
4

Study Details

Study Description

Brief Summary

Because people with undiagnosed HIV will not receive treatment and may unknowingly infect others, the investigators propose a mobile computer-based video intervention to increase HIV test rates in high volume urban hospital emergency departments (EDs). EDs offer important points of contact for many of those at greatest risk for HIV. Unfortunately, when ED patients are offered routine HIV testing, most decline. Our proposed intervention builds upon initial findings from a trial our research team conducted with patients who declined HIV testing. The intervention, grounded in the Information-Motivation and Behavioral Skills model (IMB), showed an onscreen physician explaining the importance of HIV testing (to build knowledge and motivation) and modeling a rapid HIV test (to increase motivation and behavioral skill). This brief intervention had a potent effect: a third accepted HIV testing post-intervention. While this preliminary study is highly encouraging, it revealed a number of other critical research questions. First, it remains unclear what intervention component most strongly contributed to patients' decisions to test: the video content or the offer of an HIV test by a computer rather than a person. Second, consistent with the literature, participants indicated a community member disclosing positive HIV status onscreen would increase the proportion of patients who test. Third, results suggest there is individual variation in the extent to which behavior is more strongly influenced by onscreen community members or experts (e.g. physicians). Therefore, the goal of the present study, guided by the IMB model, is to determine how the investigators can refine mobile computer-based interventions to maximize HIV testing rates among patients who initially decline to test in the ED. At the end of the computerized intervention, onscreen text will ask patients if they would agree to an HIV test. Those who agree will be tested by ED staff. The study's endpoint will be post-intervention HIV test rates. The investigators' study will inform scalable interventions for underserved populations nationwide.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: video: community member
  • Behavioral: video: physician
  • Behavioral: video: choice of video
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
None (Open Label)
Study Start Date :
Jul 1, 2014
Anticipated Primary Completion Date :
Jan 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: video: community member

Participant watches video of a community member

Behavioral: video: community member

Experimental: video: physician

Participant watches video of a physician

Behavioral: video: physician

Experimental: video: choice of video

Participant can choose to watch video of either the community member of the physician

Behavioral: video: choice of video

No Intervention: no video

Outcome Measures

Primary Outcome Measures

  1. Number of participants who accept an HIV test after completing the intervention [Day 1]

    The intervention computers will show participants a set of videos and data collection instruments. When the participant has watched the video and responded to all instruments, the computers will ask patients if they would like an HIV test. Answers are yes or no.

Secondary Outcome Measures

  1. Knowledge change [Baseline, Day 1]

    The intervention computers will display a set of HIV-related knowledge questions before and after a video segment. This will enable the investigators to examine potential increases in participants' knowledge after watching a video.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age 18 or over

  • Capable of providing informed consent

  • Reads English

  • Declined HIV test offered by hospital staf at triage

Exclusion Criteria:
  • intoxicated

  • a prisoner

  • known to be HIV positive

  • presenting to the hospital for a psychiatric problem

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Luke's Emergency Department New York New York United States 10025

Sponsors and Collaborators

  • National Development and Research Institutes, Inc.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ian Aronson, Principal Investigator, National Development and Research Institutes, Inc.
ClinicalTrials.gov Identifier:
NCT02154802
Other Study ID Numbers:
  • 1R34DA037129-01A1
First Posted:
Jun 3, 2014
Last Update Posted:
Jun 3, 2014
Last Verified:
May 1, 2014

Study Results

No Results Posted as of Jun 3, 2014