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N/A N=65 Health Services Research

PlusCare: Mobile Platform to Increase Linkage to Care in Adolescents Living With HIV/AIDS

HIV/AIDS

Enrolled (actual)
65
Serious AEs
0.0%
Results posted
Oct 2023
Primary outcome: Primary: CD4 Cell Count — 996; 1049 cells/mm^3

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
PlusCare (Device)
Age
Pediatric, Adult · 13+ yrs
Sex
All
Sponsor
Dimagi Inc.
Primary completion
Dec 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
CD4 Cell Count
996; 1049
PRIMARY
Viral Load
32.0; 24.7
PRIMARY
Appointment Adherence Rate
0.60; .67
SECONDARY
Proximal Outcomes (Monthly Medication Adherence Item)
4.7
SECONDARY
Patient-centered Outcomes (Quality of Life): Self-reported Responses to Survey
3.6; 3.6; 3.9 .03 sig
SECONDARY
Patient-centered Outcomes (Self-efficacy): Self-reported Responses to Survey
7.8; 7.8; 8.6 .02 sig
SECONDARY
System Usability (User Satisfaction): System Usability Scale
63; 51

Summary

While major advancements in medical technology over the past decade have significantly improved the life expectancy of persons infected with human immunodeficiency virus (HIV), HIV-positive youth today face new barriers to the treatment of HIV as a chronic, manageable illness. The mobile system proposed will help improve linkage to care through mobile technology support for the case management of youth living with HIV. Results of this project will determine the impact of this system on case management processes and outcomes and have implications for the care of youth living with other chronic, complex illnesses.

Eligibility Criteria

PATIENTS:

Inclusion Criteria

  • between 13-25 years old
  • HIV positive
  • enrolled in treatment at a participating study site
  • owns or has ability to access a smartphone (e.g., iPhone, Android) for one year

Exclusion Criteria

  • Non-English speaker or
  • Visually/hearing impaired

CASE MANAGERS:

Inclusion Criteria

  • Actively employed at a participating study site
  • Performs case management duties with HIV-positive patients aged 13-25 years.

Exclusion Criteria

  • (None)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03758066). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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