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

Not Applicable

Completed

Conditions: HIV/AIDS

Interventions: Device: PlusCare

Registration Number: NCT03758066

Lead Sponsor: Dimagi Inc.

Brief 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.

Detailed Description: With the advancement of medical treatments, which has contributed to the overall decrease in opportunistic infections and deaths related to human immunodeficiency virus (HIV) in youth, there is a need to ensure that youth living with HIV (YLH) are linked to and engaged in care to successfully achieve viral suppression. While an increasing number of mobile health (mHealth) technologies have been designed to address HIV prevention and care, a critical gap in innovation remains in tools designed to address the specific needs of YLH. In a Phase I project, investigators demonstrated the acceptability and feasibility of a user-centered prototype design of PlusCare, an mHealth application that can be used by YLH and their case managers (CMs) to support HIV care. Results of Phase I suggest that PlusCare could facilitate multi-disciplinary, team-based case management of YLH by supporting the sharing and signing of documents remotely, automation of adherence reminders, sharing of lab results, alerts CMs about program requirements related to age and developmental milestones, streamlining of communication between multiple members of a patient's case management team and the patient, and offering accessibility to data from multiple modalities. In this Phase II project, investigators will conduct a mixed methods, non-randomized pre-post study with CMs (N=20) and YLH patients (N=70) to examine the use of PlusCare on case management processes and health outcomes (i.e., HIV viral load, medical visit frequency and gaps) in 3 different case management programs at 2 different clinical study site settings. An initial cost analysis will be performed to assess potential cost effectiveness. Results of these Phase I and II projects will inform the development of a product that can be used in multiple case management settings and prepare PlusCare for future commercialization. Results have implications for future development of PlusCare to serve the broader HIV population (YLH aged 25-34 years old and at-risk individuals) as well as youth living with other chronic health conditions.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 65

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)

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
PlusCare	PlusCare	Patients and case managers who work with them will be given access to a web-/mobile-based application, PlusCare, to support various case management activities for one year.

Primary Outcome Measures

Name	Time	Method
Appointment Adherence Rate	1 year prior to baseline (pre), 1 year post-baseline (post)	Comparison of median appointment adherence ratio between pre and post time points, i.e., (Actual completed appointments) / (Expected appointments) where expected appointments includes completed appointments, no shows, and cancellations
CD4 Cell Count	1 year prior to baseline (pre), 1 year post-baseline (post)	Comparison of average CD4 cell count (cells/mm\^3) between pre and post time points
Viral Load	1 year prior to baseline (pre), 1 year post-baseline (post)	Comparison of average viral load (copies/mL) between pre and post time points

Secondary Outcome Measures

Name	Time	Method
Proximal Outcomes (Monthly Medication Adherence Item)	Monthly	Self-reported levels of medication adherence were reported on a monthly basis, where AYA living with HIV rated their adherence to their prescribed medication using the self-rating scale item (SRSI) single-item adherence measure. Patients reported medication adherence for the past month on a 6-point Likert scale ranging from 1 ("very poor") to 6 ("excellent"). Patients received monthly SMS text messages alerting them to report adherence via survey forms created in the PlusCare app. Mean self-reported monthly medication adherence ratings across 12 months is reported.
Patient-centered Outcomes (Self-efficacy): Self-reported Responses to Survey	1 year (Baseline, 6-month, 12-month)	Self-reported average scores to the Self-Efficacy for Managing Chronic Disease 6-item Scale (SEMCD6) were compared between 3 timepoints. SEMCD6 scores range from 1 to 10, with higher numbers indicating higher self-efficacy.
Patient-centered Outcomes (Quality of Life): Self-reported Responses to Survey	1 year (Baseline, 6-month, 12-month)	Self-reported scores to the General Health item of the CDC "Health Days Measure" Core Module (CDC HRQOL-4) item were compared between 3 timepoints, with scores ranging from 1 ("Poor") to 5 ("Excellent").
System Usability (User Satisfaction): System Usability Scale	1 year	Self-reported ratings of perceived system usability on the 10-point Likert-scaled System Usability Scale (SUS) scored in a range of 0 of 100, with higher scores indicating higher usability, were collected at end of study.