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Two Approaches to Providing HIV/AIDS Services in the Community to People Living With HIV/AIDS

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified November 2005 by McMaster University.
Recruitment status was:  Not yet recruiting
Information provided by:
McMaster University Identifier:
First received: January 20, 2006
Last updated: NA
Last verified: November 2005
History: No changes posted
This study will examine the effects of having a case manager help PHAs access and use health, social services and practical resources that are helpful to their needs as compared to the usual more PHA self-managed approach of deciding and using services as they see necessary. New and existing users of HIV/AIDS services in Wellington-Dufferin, Waterloo and Grey-Bruce Regions who consent to this study will be randomized to receive their usual self-directed supportive, educational, medical and medical care services when they seek assistance according to their needs or these usual services augmented by case management services. They will be measured before randomization and at 3, 6 and 12 months following service use for their satisfaction with HIV/AIDS services, compliance with HIV/AIDS medication, improvement in quality of life, psychological distress, risk behaviours and expenditures for the use of a range of publicly funded services.

Condition Intervention Phase
HIV Infection Behavioral: strengths-based case managed proactive service model Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: Two Approaches to Providing HIV/AIDS Services in the Community to People Living With HIV/AIDS (PHAs): The Comparative Impact on Quality of Life, Access to and Expenditures for All Health and Social Services

Resource links provided by NLM:

Further study details as provided by McMaster University:

Primary Outcome Measures:
  • risk behavior, quality of life, health and social service utilization

Secondary Outcome Measures:
  • depression, satisfaction

Estimated Enrollment: 120
Study Start Date: March 2006
Estimated Study Completion Date: February 2007

Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • HIV-positive individuals
  • living in the community setting

Exclusion Criteria:

  • cognitive impairment
  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 identifier: NCT00280449

Contact: Robin Weir, PhD 905-5259140
Contact: Karen Auld 905-5259140 ext 27237

Canada, Ontario
McMaster University Not yet recruiting
Hamilton, Ontario, Canada, L8N 3Z5
Contact: Karen Auld    905-525 9140 ext 27237   
Principal Investigator: Adriana Carvalhal, MD, PhD         
Sponsors and Collaborators
Hamilton Health Sciences Corporation
Principal Investigator: Adriana Carvalhal, MD, PhD McMaster University
  More Information Identifier: NCT00280449     History of Changes
Other Study ID Numbers: 05-357
Study First Received: January 20, 2006
Last Updated: January 20, 2006

Keywords provided by McMaster University:
people living with HIV
quality of life

Additional relevant MeSH terms:
HIV Infections
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases processed this record on September 25, 2017