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Helping HIV Infected Patients in South Africa Adhere to Drug Regimens

Primary Purpose

HIV Infections

Status
Terminated
Phase
Phase 2
Locations
South Africa
Study Type
Interventional
Intervention
Directly Observed Therapy
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Directly Observed Therapy, DOT

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: HIV infected Viral load greater than 1000 copies/ml CD4 count of 200 cells/mm3 or less, or World Health Organization Stage 4 disease Living in the area of the study site Had a known address for more than 3 months Willing to nominate a treatment supervisor (a close family member, sexual partner, friend, or community volunteer) to observe daily ingestion of tablets Willing to disclose HIV status to a treatment supervisor and ready to commit to long-term antiretroviral therapy Acceptable methods of contraception Exclusion Criteria: Pregnant

Sites / Locations

  • University of Cape Town

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

1

2

Arm Description

Use of a patient nominated peer supporter who will observe the morning dose of ARVs

Self administration of ARVs

Outcomes

Primary Outcome Measures

Impact of DOT Compared to Self-administered Treatment as Measured by HIV Viral Load at 12 Months of Treatment
Proportion of Patients with HIV RNA Levels of <400 at 12 Months - Intention-to-treat
Impact of DOT Compared to Self-administered Treatment as Measured by HIV Viral Load at 24 Months of Treatment
Proportion of Patients with HIV RNA Levels of <400 Copies/mL at 24 Months [Intention-to-treat (ITT)
Immunological Response: Median CD4 (IQR) Cell Count Increase From Baseline at 12 Months by Study Arm
Immunological Response: Median CD4 (IQR) Cell Count Increase From Baseline at 24 Months by Study Arm

Secondary Outcome Measures

Full Information

First Posted
February 3, 2004
Last Updated
March 9, 2015
Sponsor
Johns Hopkins University
Collaborators
University of Cape Town
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1. Study Identification

Unique Protocol Identification Number
NCT00076804
Brief Title
Helping HIV Infected Patients in South Africa Adhere to Drug Regimens
Official Title
DOT-HAART for HIV-Infected South African Adults
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Terminated
Why Stopped
DSMB stopped trial for futility
Study Start Date
February 2005 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Johns Hopkins University
Collaborators
University of Cape Town

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Three or more anti-HIV drugs are taken in combination as part of a treatment regimen. These drug regimens must be closely followed in order to be successful. Having a support person watch a patient take his or her anti-HIV drugs each day may help a patient follow his or her regimen. This study will see if patient-chosen treatment supporters help patients take HIV medicines correctly and improve their health. Study hypothesis: The mean change in CD4 count at 12 and 24 months will be significantly higher in the directly observed therapy-highly active antiretroviral therapy (DOT-HAART) arm as compared to the self-administered arm.
Detailed Description
South Africa has one of the worst and fastest growing HIV epidemics in the world. Highly active antiretroviral therapy (HAART) has been shown both at the individual and public health levels to reduce morbidity, mortality, and vertical and possibly horizontal HIV transmission. However, expenses, feasibility, long-term adherence, and effective delivery of HAART remain formidable barriers, particularly in developing nations. Recently, international initiatives have provided hope for widespread use of HAART at affordable cost in sub-Saharan Africa. Simplified, once-daily HAART regimens with directly observed therapy (DOT) may help to achieve high levels of treatment adherence, a key component for long-term viral suppression and treatment success. Peer advocates have been used to improve adherence with medical therapies in a variety of settings. This study will evaluate the effectiveness and feasibility of DOT using patient-nominated peer supervisors to improve adherence to HAART in HIV infected adults in South Africa. Participants will be randomly assigned to either Peer-DOT-HAART or self-administration of a once-daily combination of the Western Cape Province ART program medications for 24 months. Study measures will include CD4 cell count and HIV viral load, adherence questionnaires, genotypic HAART resistance testing, and incidence of new or recurrent opportunistic infections.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Directly Observed Therapy, DOT

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
274 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Use of a patient nominated peer supporter who will observe the morning dose of ARVs
Arm Title
2
Arm Type
No Intervention
Arm Description
Self administration of ARVs
Intervention Type
Behavioral
Intervention Name(s)
Directly Observed Therapy
Intervention Description
Use of a patient nominated peer supporter who will observe the morning dose of ARVs
Primary Outcome Measure Information:
Title
Impact of DOT Compared to Self-administered Treatment as Measured by HIV Viral Load at 12 Months of Treatment
Description
Proportion of Patients with HIV RNA Levels of <400 at 12 Months - Intention-to-treat
Time Frame
at 12 and 24 months of treatment
Title
Impact of DOT Compared to Self-administered Treatment as Measured by HIV Viral Load at 24 Months of Treatment
Description
Proportion of Patients with HIV RNA Levels of <400 Copies/mL at 24 Months [Intention-to-treat (ITT)
Time Frame
24 months
Title
Immunological Response: Median CD4 (IQR) Cell Count Increase From Baseline at 12 Months by Study Arm
Time Frame
12 months
Title
Immunological Response: Median CD4 (IQR) Cell Count Increase From Baseline at 24 Months by Study Arm
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV infected Viral load greater than 1000 copies/ml CD4 count of 200 cells/mm3 or less, or World Health Organization Stage 4 disease Living in the area of the study site Had a known address for more than 3 months Willing to nominate a treatment supervisor (a close family member, sexual partner, friend, or community volunteer) to observe daily ingestion of tablets Willing to disclose HIV status to a treatment supervisor and ready to commit to long-term antiretroviral therapy Acceptable methods of contraception Exclusion Criteria: Pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard E Chaisson, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Cape Town
City
Cape Town
ZIP/Postal Code
7925
Country
South Africa

12. IPD Sharing Statement

Citations:
PubMed Identifier
20453627
Citation
Nachega JB, Chaisson RE, Goliath R, Efron A, Chaudhary MA, Ram M, Morroni C, Schoeman H, Knowlton AR, Maartens G. Randomized controlled trial of trained patient-nominated treatment supporters providing partial directly observed antiretroviral therapy. AIDS. 2010 Jun 1;24(9):1273-80. doi: 10.1097/QAD.0b013e328339e20e.
Results Reference
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Helping HIV Infected Patients in South Africa Adhere to Drug Regimens

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