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A Study of Two Adherence Plans to Help HIV-Positive Patients Take Their Medications Correctly

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Electronic Medication Reminder System
Medication Manager
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Drug Therapy, Combination, RNA, Viral, Patient Compliance, Anti-HIV Agents, Viral Load, Reminder Systems, Treatment Experienced, Treatment Naive

Eligibility Criteria

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

Inclusion Criteria Patients may be eligible for this study if they: Are enrolling in a qualifying CPCRA AR therapeutic study. Currently, the FIRST and MDR-HIV studies are the only qualifying protocols. Exclusion Criteria Patients will not be eligible for this study if they: Are enrolling at a clinic site that is unable to participate in this study for some reason.

Sites / Locations

  • Community Consortium / UCSF
  • Virginia Cafaro M.D.
  • Denver CPCRA / Denver Public Hlth
  • Univ Hosp Infectious Diseases Clinic
  • Yale Univ School of Medicine / AIDS Program
  • Washington Reg AIDS Prog / Dept of Infect Dis
  • AIDS Research Consortium of Atlanta
  • AIDS Research Alliance - Chicago
  • Louisiana Comm AIDS Rsch Prog / Tulane Univ Med
  • Wayne State Univ - WSU/DMC / Univ Hlth Ctr
  • Henry Ford Hosp
  • Southern New Jersey AIDS Clinical Trials
  • North Jersey Community Research Initiative
  • Partners in Research / New Mexico
  • Bronx-Lebanon Hosp Ctr
  • Harlem AIDS Treatment Grp / Harlem Hosp Ctr
  • The Research and Education Group
  • Philadelphia FIGHT
  • Univ TX Health Science Ctr
  • Richmond AIDS Consortium / Div of Infect Diseases

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
January 17, 2000
Last Updated
September 28, 2013
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00001129
Brief Title
A Study of Two Adherence Plans to Help HIV-Positive Patients Take Their Medications Correctly
Official Title
Adherence Strategies Using a Medication Manager and an Electronic Medication Reminder System for HIV-Infected Patients Receiving HAART
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2003 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to look at different ways to help patients follow their anti-HIV medication schedules. It is very important that HIV-positive patients take their anti-HIV medications correctly so they get the best possible benefit from them. Taking the drugs correctly, called "adherence," may keep HIV virus levels in the blood (viral load) low for a longer time. However, anti-HIV medication schedules are often complicated, and many patients have difficulty remembering to take their drugs at the correct time. This study will look at 2 different ways to teach patients about the importance of taking their medications correctly and to remind them when to take their medications.
Detailed Description
Adherence to antiretroviral (AR) therapy has become increasingly important in the management of HIV infection. Adherence to AR regimens is thought to be a critical factor in maintaining therapeutic drug levels, thus helping ensure viral suppression and minimizing the risk of drug resistance. However, AR regimens are often complex with demanding dosing schedules. Patients often miss doses because they simply forget; other factors such as substance abuse, depression, and low literacy levels also contribute to nonadherence. Adherence is influenced not only by individual behavior but also by the services, the quality of the patient-provider relationship, and the amount of social support offered the patient. There is no currently agreed upon, widely used, and generalizable intervention for improving adherence over the long course of HIV therapy. This study provides a long-term comparative evaluation of two interventions. Clinical sites, rather than individual patients, are randomized to one of four groups: a medication manager, an electronic medication reminder system, a medication manager plus an electronic medication reminder system, or usual care. Special training sessions are held for the staff of participating units assigned to medication manager and/or electronic medication reminder system interventions. The medication manager is a research staff member who works individually with study patients, addressing the knowledge, motivation, and skills necessary for adherence. The electronic medication reminder system is ALR (A Little Reminder). This is a small, portable alarm that is programmed to sound and flash at the times of the patient's scheduled AR medication doses. Patients enrolling into either the FIRST or MDR-HIV study at clinical sites authorized to carry out this study are offered the option of participating in the adherence intervention to which the clinical site has been randomly assigned. Data collected through the FIRST and the MDR-HIV protocols are used to address the Adherence study objectives. Patients on the FIRST protocol are assessed for time to first plasma HIV-RNA level above 2,000 copies/ml. Also, patients on the FIRST and MDR-HIV studies are assessed for changes in viral load, resistance, CD4 cell counts, adherence, and other factors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Drug Therapy, Combination, RNA, Viral, Patient Compliance, Anti-HIV Agents, Viral Load, Reminder Systems, Treatment Experienced, Treatment Naive

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Enrollment
1248 (false)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Electronic Medication Reminder System
Intervention Type
Behavioral
Intervention Name(s)
Medication Manager

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients may be eligible for this study if they: Are enrolling in a qualifying CPCRA AR therapeutic study. Currently, the FIRST and MDR-HIV studies are the only qualifying protocols. Exclusion Criteria Patients will not be eligible for this study if they: Are enrolling at a clinic site that is unable to participate in this study for some reason.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sharon Mannheimer
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Edward Morse
Official's Role
Study Chair
Facility Information:
Facility Name
Community Consortium / UCSF
City
San Francisco
State/Province
California
ZIP/Postal Code
94110
Country
United States
Facility Name
Virginia Cafaro M.D.
City
San Francisco
State/Province
California
ZIP/Postal Code
94110
Country
United States
Facility Name
Denver CPCRA / Denver Public Hlth
City
Denver
State/Province
Colorado
ZIP/Postal Code
80204
Country
United States
Facility Name
Univ Hosp Infectious Diseases Clinic
City
Denver
State/Province
Colorado
ZIP/Postal Code
80204
Country
United States
Facility Name
Yale Univ School of Medicine / AIDS Program
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06510
Country
United States
Facility Name
Washington Reg AIDS Prog / Dept of Infect Dis
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20422
Country
United States
Facility Name
AIDS Research Consortium of Atlanta
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30308
Country
United States
Facility Name
AIDS Research Alliance - Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60657
Country
United States
Facility Name
Louisiana Comm AIDS Rsch Prog / Tulane Univ Med
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States
Facility Name
Wayne State Univ - WSU/DMC / Univ Hlth Ctr
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Henry Ford Hosp
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
Facility Name
Southern New Jersey AIDS Clinical Trials
City
Camden
State/Province
New Jersey
ZIP/Postal Code
08103
Country
United States
Facility Name
North Jersey Community Research Initiative
City
Newark
State/Province
New Jersey
ZIP/Postal Code
07103
Country
United States
Facility Name
Partners in Research / New Mexico
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87131
Country
United States
Facility Name
Bronx-Lebanon Hosp Ctr
City
Bronx
State/Province
New York
ZIP/Postal Code
10453
Country
United States
Facility Name
Harlem AIDS Treatment Grp / Harlem Hosp Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10037
Country
United States
Facility Name
The Research and Education Group
City
Portland
State/Province
Oregon
ZIP/Postal Code
97210
Country
United States
Facility Name
Philadelphia FIGHT
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Univ TX Health Science Ctr
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Richmond AIDS Consortium / Div of Infect Diseases
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23298
Country
United States

12. IPD Sharing Statement

Learn more about this trial

A Study of Two Adherence Plans to Help HIV-Positive Patients Take Their Medications Correctly

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