CClinicalTrials.gg
CompletedNCT00300183Updated Jan 8, 2019

Evaluation of an HIV Outreach Program

An observational study in HIV Infections, sponsored by Montefiore Medical Center. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-01-08.

Sponsored by Montefiore Medical Center · Observational

Study type
Observational
Time perspective
Other
Enrollment
150
Ages
18 Years and older
Sex
All
01

Study summary

This study evaluates outreach to HIV-infected people living in unstable housing in New York City who are new to CitiWide Harm Reduction. One hundred and fifty people are interviewed every 6 months, and their medical records are reviewed every 6 months for a total of 18 months. The study examines how outreach, case management, housing, drug use, mental health, and quality of life are related to people's ability to get into and stay in medical care.

Read the detailed description

The study is a prospective cohort study in which 150 newly enrolled HIV-infected participants of CitiWide Harm Reduction are followed for 18 months to assess HIV-related health outcomes. Data elements include (1) face-to-face interviews focusing on housing, HIV disease severity, utilization of health care services, utilization of non-medical services, substance use, mental health, and quality of life; (2) medical chart information focusing on CD4 count, viral load, and HIV primary care visits; and (3) outreach services. The study hypothesis is that involvement with CitiWide Harm Reduction will improve HIV-related health care utilization and outcomes.

02

Conditions studied

  • HIV Infections

Browse trials for

Keywords

  • HIV
  • health services accessibility
  • health services research
  • homeless
  • social support
  • AIDS
  • substance abuse
  • mental health
  • quality of life
  • outreach
  • harm reduction
03

In context

HIV Infections

4,258 studies on the registry are indexed under HIV Infections; 240 are open to participants now.

This study's enrollment of 150 is below the median of 200 across 713 observational studies indexed under HIV Infections.

Browse HIV Infections studies →

Lead sponsor

Montefiore Medical Center is the lead sponsor of 402 studies on the registry; 70 are open to participants now.

Of its 81 completed or terminated interventional studies of FDA-regulated products, 73 (90%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • HIV-infected, living in one of 15 single room occupancy hotels served by CitiWide Harm Reduction, new to CitiWide Harm Reduction, at least 18 years of age, English or Spanish speaking

Exclusion criteria

Exclusion Criteria:

  • HIV-negative
05

Study design

Time perspective
Other
Enrollment
150 participants
06

Study locations

1 site
  • Montefiore Medical Center
    Bronx, New York 10467, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 8, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00300183
Lead sponsor
Montefiore Medical Center
Collaborators
Health Resources and Services Administration (HRSA), CitiWide Harm Reduction
Responsible party
Sponsor
First posted
Mar 8, 2006
Start date
Oct 2003
Primary completion
Jul 31, 2005
Completion
Jul 31, 2005
Last update
Jan 8, 2019

Study contacts

Chinazo O Cunningham, MD
principal investigator · Montefiore Medical Center
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2005. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion