Evaluation of an HIV Outreach Program

This study has been completed.
Sponsor:
Collaborators:
HRSA/Maternal and Child Health Bureau
CitiWide Harm Reduction
Information provided by:
Montefiore Medical Center
ClinicalTrials.gov Identifier:
NCT00300183
First received: March 7, 2006
Last updated: March 31, 2006
Last verified: September 2005
  Purpose

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.


Condition
HIV Infections

Study Type: Observational
Study Design: Observational Model: Defined Population
Time Perspective: Longitudinal
Official Title: Evaluation of an Outreach and Intervention Program to Reach HIV- Positive Persons Living in Bronx, NY Single Room Occupancy Hotels

Resource links provided by NLM:


Further study details as provided by Montefiore Medical Center:

Estimated Enrollment: 150
Study Start Date: October 2003
Estimated Study Completion Date: July 2005
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. We hypothesize that involvement with CitiWide Harm Reduction will improve HIV-related health care utilization and outcomes.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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:

  • HIV-negative
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00300183

Locations
United States, New York
Montefiore Medical Center
Bronx, New York, United States, 10467
Sponsors and Collaborators
Montefiore Medical Center
HRSA/Maternal and Child Health Bureau
CitiWide Harm Reduction
Investigators
Principal Investigator: Chinazo O Cunningham, MD Montefiore Medical Center
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00300183     History of Changes
Other Study ID Numbers: #2H97 HA 00247-03-02
Study First Received: March 7, 2006
Last Updated: March 31, 2006
Health Authority: United States: Institutional Review Board

Keywords provided by Montefiore Medical Center:
HIV
health services accessibility
health services research
homeless
social support
AIDS
substance abuse
mental health
quality of life
outreach
harm reduction

Additional relevant MeSH terms:
HIV Infections
Acquired Immunodeficiency Syndrome
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Slow Virus Diseases

ClinicalTrials.gov processed this record on September 30, 2014