HIV Clinical Trial
— ARTCo-opsOfficial title:
Developing and Assessing a Community Based Model of Antiretroviral Care
Tremendous efforts and resources have been expended by the global community to ensure that
antiretroviral therapy (ART) is available and accessible to all that need it. Despite these,
less than a half of Human Immunodeficiency Virus (HIV)-infected patients requiring ART in
sub-Saharan Africa (SSA) are receiving it. Some of the most significant barriers to
attaining universal access to ART in this region include large distances that patients have
to travel to clinic, time spent in accessing care and a significant shortage of human
resources. In order to address these challenges the World Health Organization (WHO)
advocates alternative care models especially those that incorporate task-shifting to lower
cadre health care workers and lay persons. Unfortunately, few such alternative care models
have been identified and very little data exist on their long-term outcomes.
With this project we will develop and assess an alternative care model that is established
on the platform of a HIV-infected peer-group (ART Co-op) and facilitated by community health
workers (CHW's). This model of care is intended to decentralize ART services and bring them
closer to the patients. Specifically, we will:
1. Develop an acceptable and sustainable model for extending HIV care and treatment into
the community.
2. Perform a pilot study comparing the outcomes of patients enrolled in the ART Co-ops
program to those receiving standard of care.
3. Determine the cost savings and cost effectiveness of ART Co-ops.
| Status | Not yet recruiting |
| Enrollment | 360 |
| Est. completion date | December 2016 |
| Est. primary completion date | December 2016 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: 1. HIV-infected 2. =18 years old 3. Have a current cluster of differentiation 4 (CD4)count =200cells/µl 4. Have an undetectable VL 5. Are clinically stable on ART for = 6 months 6. A resident of a sub-location within the AMPATH Kitale clinic catchment area 7. Are willing to consent to participate Exclusion Criteria: 1. Pregnant 2. Active opportunistic infection (OI) 3. Unable to consent for study participation due to physical or mental incapacity |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Moi University | Centers for Disease Control and Prevention |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | ART durability | Durability of ART regimen (ART failure). This is defined as the need to change ART regimens based on clinical (new or recurrent WHO 3 or 4 event), immunologic (CD4 count< pre-ART; =50% CD4 decrease from peak; persistent CD4<100) or virologic failure (VL>10,000 copies/mL). Durability of the patient's ART regimen (requiring no change to second line for failure) will remain equivalent to those seen in clinic regularly. | 48 weeks | No |
| Secondary | Retention in care | Retention between the two groups will be compared at 48 weeks. | 48 weeks | No |
| Secondary | HIV VL (copies/mL) | Plasma viral load changes at 48 weeks will be measured | 48 weeks | No |
| Secondary | Quality of life | Quality of life at 48 weeks will be measured using a questionnaire | 48 weeks | No |
| Secondary | stigma | Stigma levels at 48 weeks will be measured using a questionnaire | 48 weeks | No |
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