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Managed Problem Solving to Increase Treatment Adherence in Individuals With HIV (MAPS)

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Managed problem solving
Standard care
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring HIV, AIDS, Problem Solving, Antiretroviral Therapy, Highly Active, Patient Compliance

Eligibility Criteria

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

Inclusion Criteria for All Participants: HIV infected Infection likely to be susceptible to a specific treatment regimen Have access to a telephone Willing and able to comply with all study requirements Exclusion Criteria for All Participants: Live in a care facility that provides medications on schedule Inclusion Criteria for Treatment-Experienced Participants: Restarting HAART after a treatment interruption of at least 3 months OR after virologic failure with a viral load greater than 1,000 copies/ml On a treatment regimen for less than 2 weeks prior to study entry

Sites / Locations

  • University of Pennsylvania School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Participants will receive managed problem solving for 12 months

Participants will receive standard of care for 12 months

Outcomes

Primary Outcome Measures

Improved adherence

Secondary Outcome Measures

Decrease in viral load
Increase in CD4 count

Full Information

First Posted
August 11, 2005
Last Updated
July 12, 2012
Sponsor
University of Pennsylvania
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00130273
Brief Title
Managed Problem Solving to Increase Treatment Adherence in Individuals With HIV
Acronym
MAPS
Official Title
Managed Problem Solving: An HIV Adherence Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
July 2005 (undefined)
Primary Completion Date
February 2011 (Actual)
Study Completion Date
February 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pennsylvania
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

5. Study Description

Brief Summary
This study will determine whether a managed problem solving intervention can help patients with HIV better follow their anti-HIV drug regimen and can control HIV better than the standard of care.
Detailed Description
HAART is considered to be the most effective treatment for HIV. However, sustained and consistent adherence to HAART is necessary for long-term success. Issues such as memory problems, lack of social support, medication side effects, depression, and substance abuse can significantly reduce patient adherence to HAART. This study will evaluate the effectiveness of a managed problem solving strategy to increase HAART adherence in patients with HIV. Both treatment-naive and treatment-experienced participants will be recruited for this study. The treatment part of this study will last 12 months. Participants will be randomly assigned to receive the managed problem solving intervention or standard of care for 12 months. Participants in the managed problem solving group will have 4 study visits and will receive 3 phone calls for the first 3 months of the study, and 1 phone call every month for the following 9 months. At each study visit, participants will identify barriers to adherence. During the phone calls, participants will be asked about any steps they have taken to improve their adherence. A medication event monitoring system (MEMS) will be used to assess participants' treatment adherence. MEMS uses microelectronic monitors on the caps of medication bottles to record the timing and frequency of bottle openings. Participants whose adherence has decreased or remained the same at the end of 12 months will be evaluated for regimen changes. Blood collection at the beginning and end of the study will be used to measure viral load and CD4 count. Follow-up phone interviews will be conducted every year for 3 years after the end of treatment. Study hypothesis: Managed problem solving will result in better adherence to highly active antiretroviral therapy (HAART) and better virologic control and immunological outcomes at the end of 1 year compared with a control group receiving standard or care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
HIV, AIDS, Problem Solving, Antiretroviral Therapy, Highly Active, Patient Compliance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
180 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Participants will receive managed problem solving for 12 months
Arm Title
2
Arm Type
Active Comparator
Arm Description
Participants will receive standard of care for 12 months
Intervention Type
Behavioral
Intervention Name(s)
Managed problem solving
Intervention Description
Participants in the managed problem solving group will have four study visits and will receive three phone calls for the first 3 months of the study, and one phone call every month for the following 9 months. At each study visit, participants will identify barriers to adherence. During the phone calls, participants will be asked about any steps they have taken to improve their adherence. A medication event monitoring system (MEMS) will be used to assess participants' treatment adherence. MEMS uses microelectronic monitors on the caps of medication bottles to record the timing and frequency of bottle openings. Participants whose adherence has decreased or remained the same at the end of 12 months will be evaluated for regimen changes. Blood collection at the beginning and end of the study will be used to measure viral load and CD4 count.
Intervention Type
Behavioral
Intervention Name(s)
Standard care
Intervention Description
Participants will receive standard of care for 12 months.
Primary Outcome Measure Information:
Title
Improved adherence
Time Frame
Measured at Year 4
Secondary Outcome Measure Information:
Title
Decrease in viral load
Time Frame
Measured at Year 4
Title
Increase in CD4 count
Time Frame
Measured at Year 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria for All Participants: HIV infected Infection likely to be susceptible to a specific treatment regimen Have access to a telephone Willing and able to comply with all study requirements Exclusion Criteria for All Participants: Live in a care facility that provides medications on schedule Inclusion Criteria for Treatment-Experienced Participants: Restarting HAART after a treatment interruption of at least 3 months OR after virologic failure with a viral load greater than 1,000 copies/ml On a treatment regimen for less than 2 weeks prior to study entry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Gross, MD, MSCE
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pennsylvania School of Medicine
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23358784
Citation
Gross R, Bellamy SL, Chapman J, Han X, O'Duor J, Palmer SC, Houts PS, Coyne JC, Strom BL. Managed problem solving for antiretroviral therapy adherence: a randomized trial. JAMA Intern Med. 2013 Feb 25;173(4):300-6. doi: 10.1001/jamainternmed.2013.2152.
Results Reference
derived

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Managed Problem Solving to Increase Treatment Adherence in Individuals With HIV

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