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Group Clinical Visit Adherence Intervention for HIV+ Women of Color

Primary Purpose

Adherence, Patient, HIV/AIDS, Group Meetings

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sisters-GPS: Group Clinical Visits
Control: One-on-one Adherence Counseling
Sponsored by
Montefiore Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Adherence, Patient focused on measuring HIV treatment, Adherence Group Treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion criteria:

  1. HIV-positive
  2. Cis gender women (assigned female sex at birth and current identifies as female)
  3. ≥ 18 years old
  4. English proficiency
  5. At least one visit to community health center where received HIV primary care within the last 12 months
  6. Self-reported ARV adherence <100% in the previous 30 days
  7. Most recent HIV viral load in last 12 months detectable
  8. Prescribed HIV medications for at least 16 weeks prior to detectable HIV viral load
  9. Currently prescribed HIV medications (i.e., current active HIV medication prescription in electronic medical record or pharmacy)
  10. Able to attend most/all group visits

Exclusion Criteria:

  1. Untreated severe mental illness including major depressive disorder, bipolar disorder, schizophrenia, psychosis, or current suicidal ideation.
  2. Acute intoxication

Sites / Locations

  • Montefiore Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sisters-GPS: Group Clinical Visits

Control: One-on-one Adherence Counseling

Arm Description

Those randomized to the Sisters-GPS arm will be expected to attend a total of seven group clinical visits, once a week for ~1.5 hours. Groups visits will include education, self-management skills development, and a clinical assessment by a medical provider with a focus on HIV treatment and adherence. Additionally, Sisters-GPS participants will be encouraged to participate in a private social media site specifically designed for the study, where participants will be able communicate with one another and with research staff. Group size will be 8-10 participants.

Those randomized to the control condition will receive an appointment with a HIV treatment adherence counselor and will be expected to attend a minimum of three adherence counseling visits. .

Outcomes

Primary Outcome Measures

Antiretroviral Therapy (ARV) adherence
Pill count, self-report

Secondary Outcome Measures

Change in HIV viral load
Change in HIV viral load from baseline to 8 weeks modeled as continuous variable
HIV Viral Load (VL) suppression
HIV VL used as a dichotomous measure (VL<40 copies/mL, yes/no)
Antiretroviral Therapy (ARV) adherence
Pill count, self-report
Antiretroviral Therapy (ARV) adherence
Pill count, self-report
HIV Viral Load (VL) suppression
HIV VL used as a dichotomous measure (VL<40 copies/mL, yes/no)
Change in HIV viral load
Change in HIV viral load from baseline to 8 weeks modeled as continuous variable

Full Information

First Posted
April 6, 2017
Last Updated
June 6, 2018
Sponsor
Montefiore Medical Center
Collaborators
National Institutes of Health (NIH), Albert Einstein College of Medicine, National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT03109743
Brief Title
Group Clinical Visit Adherence Intervention for HIV+ Women of Color
Official Title
Development and Testing of a Group Clinical Visit Adherence Intervention for HIV+ Women of Color
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Terminated
Why Stopped
The funding for the study was relinquished and so study terminated early.
Study Start Date
May 17, 2017 (Actual)
Primary Completion Date
December 7, 2017 (Actual)
Study Completion Date
December 7, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Montefiore Medical Center
Collaborators
National Institutes of Health (NIH), Albert Einstein College of Medicine, National Institute of Mental Health (NIMH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators will conduct a pilot randomized controlled trial (RCT) of Sisters-GPS with HIV-positive women of color with suboptimal ARV adherence and detectable HIV viral loads (VL). Participants will be randomized to Sisters-GPS (intervention involving weekly group clinical visits for seven weeks plus social media website) or appointment with an adherence counselor (a minimum of 3 visits) (control condition). Data sources will include interviews, medical and pharmacy records, and blood samples. The primary outcome will be ARV adherence at the completion of the intervention assessed via pill count. The secondary outcome will be HIV VL suppression.
Detailed Description
African American and Latina women comprise about 80% of the approximately 300,000 HIV-positive women in the United States. HIV/AIDS is one of the leading causes of death among African American and Latina women age 20 to 55 years. HIV-positive women of color are disproportionately impacted by poverty and other factors such as substance abuse and mental illness which increase vulnerability to HIV and risk of poor health outcomes (e.g., progression to AIDS and death). The stages of HIV treatment cascade include linkage to and retention in HIV care, antiretroviral (ARV) utilization, and viral suppression. While all of these stages are important, what has ultimately lengthened life expectancy among HIV-positive persons has been achieving long-term viral suppression by optimizing ARV adherence. Suboptimal ARV adherence is associated with increased risk of progression to AIDS, mortality, and the development of ARV resistance. Recent studies indicate that significant racial and ethnic disparities in ARV adherence persist, with African Americans and Latinos having lower levels of adherence than whites. This disparity is also reflected among HIV+ women, with women of color, and in particular African American women, having significantly lower rates of ARV adherence than white women. Peer-based health interventions have been shown to affect behavior and improve patient outcomes. For HIV-positive persons, receiving care within a group of peers is associated with decreased levels of shame, HIV-related stigma, and risk behaviors, and increased levels of perceived social support. A group-based approach to care involving peers may be especially important for HIV-positive women of color as HIV-positive women of color may lack positive social support. Consequently, the peer-group dynamic may help not only to normalize living with HIV and provide social support but also to motivate healthy behaviors such as ARV adherence. Group clinical visits, in which the same group of patients who share a common medical condition receives care simultaneously from a health care provider over time, is a model of care that seeks to take advantage of the peer-group dynamic. This model often includes a clinical assessment, education, and self-management skills development, all in the group setting. It has been utilized in the care of patients with chronic conditions such as diabetes mellitus and Hepatitis C infection and improves health outcomes. Therefore, guided by an enhanced version of the Social Learning Theory, which posits that people learn not only from their own experiences but from the experiences and actions of others, the investigators will tailor the group clinical visit model to a model of group HIV treatment focused on optimizing ARV adherence. Use of social media, whereby people interact by creating, sharing, and exchanging content using internet-based technologies, transcends race/ethnicity and socioeconomic status. Within the arena of health care, its use is becoming increasingly popular. For example, social media is used by persons who may have a common medical condition, such as HIV, to communicate about coping with the disease or taking medications. Among HIV-positive persons, social media may be used to enhance communication and social support; hence, the investigators have incorporated social media as a component of Sisters-GPS. To begin to address disparities in ARV adherence and the limitations of current interventions, the investigators will test Sisters-GPS, an intervention for HIV-positive women of color with suboptimal ARV adherence that the investigators have developed. Sisters-GPS is an intervention adapted from the group clinical visit and which incorporated social media. If proven effective, this intervention has the potential to be a model of health care delivery for HIV care and treatment, more generally, and can be disseminated to diverse clinical settings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adherence, Patient, HIV/AIDS, Group Meetings
Keywords
HIV treatment, Adherence Group Treatment

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The investigators pilot test efficacy of Sisters-GPS intervention in improving ARV adherence by randomizing 60 HIV+ women of color with suboptimal ARV adherence and detectable HIV viral loads (VL) to Sisters-GPS, group clinical visits, or to an appointment with an adherence counselor. The investigators will collect data from interviews, pill counts, medical and pharmacy records, and blood samples. The study's primary outcome will be ARV adherence assessed by pill count at 8 weeks; secondary outcome will be change in HIV VL from baseline to 8 weeks.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sisters-GPS: Group Clinical Visits
Arm Type
Experimental
Arm Description
Those randomized to the Sisters-GPS arm will be expected to attend a total of seven group clinical visits, once a week for ~1.5 hours. Groups visits will include education, self-management skills development, and a clinical assessment by a medical provider with a focus on HIV treatment and adherence. Additionally, Sisters-GPS participants will be encouraged to participate in a private social media site specifically designed for the study, where participants will be able communicate with one another and with research staff. Group size will be 8-10 participants.
Arm Title
Control: One-on-one Adherence Counseling
Arm Type
Active Comparator
Arm Description
Those randomized to the control condition will receive an appointment with a HIV treatment adherence counselor and will be expected to attend a minimum of three adherence counseling visits. .
Intervention Type
Behavioral
Intervention Name(s)
Sisters-GPS: Group Clinical Visits
Intervention Description
Sisters-GPS will be involve group clinical visits where by the same group participants with meet with a clinician and behaviorist to receive education, self-management skills development, and clinical assessment over the seven weekly group visits. The content will focus specifically on HIV medications and medication adherence. Additionally, the intervention will involve a private social media website where participants will be able to engage with one another between group clinical visits. Participants will receive food and a roundtrip Metrocard at each group clinical visit.
Intervention Type
Behavioral
Intervention Name(s)
Control: One-on-one Adherence Counseling
Intervention Description
For participants in the control arm, the counselor will provide standard-of-care adherence counseling, which includes education about ARVs and the importance of adherence, and addressing non-adherence including assessment of psychosocial barriers to adherence. For visits to the adherence counselor, participants will receive round-trip MetroCards as per clinic policy. Control arm participants will be expected to attend a minimum of three visits with the adherence counselor.
Primary Outcome Measure Information:
Title
Antiretroviral Therapy (ARV) adherence
Description
Pill count, self-report
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Change in HIV viral load
Description
Change in HIV viral load from baseline to 8 weeks modeled as continuous variable
Time Frame
8 weeks
Title
HIV Viral Load (VL) suppression
Description
HIV VL used as a dichotomous measure (VL<40 copies/mL, yes/no)
Time Frame
8 weeks
Title
Antiretroviral Therapy (ARV) adherence
Description
Pill count, self-report
Time Frame
4 weeks
Title
Antiretroviral Therapy (ARV) adherence
Description
Pill count, self-report
Time Frame
20 weeks
Title
HIV Viral Load (VL) suppression
Description
HIV VL used as a dichotomous measure (VL<40 copies/mL, yes/no)
Time Frame
20 weeks
Title
Change in HIV viral load
Description
Change in HIV viral load from baseline to 8 weeks modeled as continuous variable
Time Frame
20 weeks
Other Pre-specified Outcome Measures:
Title
ARV beliefs and attitudes
Description
Measure using an ARV beliefs and attitudes questionnaire
Time Frame
at baseline, 4 weeks, 8 weeks, 20 weeks
Title
ARV Knowledge
Description
Measure using a HIV Treatment Knowledge Scale
Time Frame
at baseline, 4 weeks, 8 weeks, 20 weeks
Title
Medication side effects
Description
Measure using Treatment Satisfaction Questionnaire for Medication
Time Frame
at baseline, 4 weeks, 8 weeks, 20 weeks
Title
Perceived self-efficacy
Description
Measure using an ARV adherence Self-Efficacy Scale
Time Frame
at baseline, 4 weeks, 8 weeks, 20 weeks
Title
Perceived HIV-related stigma
Description
Measure using the HIV Stigma Scale
Time Frame
at baseline, 4 weeks, 8 weeks, 20 weeks
Title
Perceived social support
Description
Measured using Scale of Perceived Social Support
Time Frame
at baseline, 4 weeks, 8 weeks, 20 weeks

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Individual assigned female sex at birth and who currently identify as female.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria: HIV-positive Cis gender women (assigned female sex at birth and current identifies as female) ≥ 18 years old English proficiency At least one visit to community health center where received HIV primary care within the last 12 months Self-reported ARV adherence <100% in the previous 30 days Most recent HIV viral load in last 12 months detectable Prescribed HIV medications for at least 16 weeks prior to detectable HIV viral load Currently prescribed HIV medications (i.e., current active HIV medication prescription in electronic medical record or pharmacy) Able to attend most/all group visits Exclusion Criteria: Untreated severe mental illness including major depressive disorder, bipolar disorder, schizophrenia, psychosis, or current suicidal ideation. Acute intoxication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oni Blackstock, MD, MHS
Organizational Affiliation
Montefiore Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Group Clinical Visit Adherence Intervention for HIV+ Women of Color

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