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Completed

NCT Number: NCT03758066

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

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.

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

PlusCare

Device

PlusCare is a mobile application designed to be used by youth and young adults with HIV and case managers.

Primary outcomes

  1. CD4 Cell Count

    Time frame: 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

  2. Viral Load

    Time frame: 1 year prior to baseline (pre), 1 year post-baseline (post)

    Comparison of average viral load (copies/mL) between pre and post time points

  3. Appointment Adherence Rate

    Time frame: 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

Secondary outcomes

  1. Proximal Outcomes (Monthly Medication Adherence Item)

    Time frame: 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.

  2. Patient-centered Outcomes (Quality of Life): Self-reported Responses to Survey

    Time frame: 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").

  3. Patient-centered Outcomes (Self-efficacy): Self-reported Responses to Survey

    Time frame: 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.

  4. System Usability (User Satisfaction): System Usability Scale

    Time frame: 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.

Sponsors and collaborators

Lead sponsor

Dimagi Inc.

Industry

Collaborators

  • Boston Children's Hospital
  • Boston Medical Center

Registry information

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Nov 29, 2018
Registry last updated
Oct 26, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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