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mHealth App for Engagement in Care Among Youth Living With HIV

Primary Purpose

HIV/AIDS, Mobile Health, Young Adults

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mobile Health Application
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for HIV/AIDS focused on measuring Health Disparity

Eligibility Criteria

18 Years - 29 Years (Adult)All SexesDoes not accept healthy volunteers

Eligibility Criteria:

  • Must be between 18 and 29 years of age
  • Must be living with HIV
  • Must reside and/or get care in San Francisco Bay Area
  • Must be able to provide informed consent to be a research participant
  • Must be able to speak and understand English
  • Must have access to an Android (5.0 or higher) or iOS (10.0 or higher) mobile phone

Exclusion Criteria:

Evidence of cognitive impairment or psychotic disorder that prevents one from understanding the purpose of the study and/or participating fully in study activities. This determination will be made by trained study staff in consultation with the principal investigator.

Sites / Locations

  • University of California San Francisco, Mission Bay Campus

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Arm 1: Intervention

Arm Description

All YLWH who choose to enroll in the study will receive access to WYZ, the mobile health application. The participants will be asked to use the app for 6 months, during which the investigators will assess the feasibility and acceptability of WYZ. Based on this initial data, the investigators will refine and release a new version of the app (WYZ 3.0).

Outcomes

Primary Outcome Measures

Feasibility: Rate of Participant Recruitment
Recruit at least 55 participants (i.e. 70% of target N)
Feasibility: Frequency of WYZ Access
Percentage of participants who achieve an average of 1 log-in per week
Feasibility: Length of Session (Minutes)
Percentage of participants who achieve an average of 15 minutes in application per week
Feasibility: Rate of Use of Refill Reminders
Percentage of participants that use feature once monthly (if receiving 30-day ART supply)
Feasibility: Rate of Use of ART Adherence Tracking
Percentage of participants that track med adherence at least 3 times per week
Feasibility: Rate of Access of Laboratory Data
Percentage of participants that review laboratory data at least one-time per month
Feasibility: Rate of Communication With Clinical Team Members
Percentage of participants who achieve an average of 1 communication exchange per month with clinical team member
Feasibility: Rate of Communication With Peers
Percentage of participants who achieve an average of one post or response to a post per week
Feasibility: Rate of Access of Health News
Percentage of participants who review health news at least once per week
Feasibility: Rate of Access of Event Calendar
Percentage of participants who review event calendar at least once per week
Feasibility: Time For Participant Onboarding (Minutes)
Average time to onboard new participant (including downloading app and reviewing app features)
Feasibility: Time To Maintain & Support (Minutes)
Average time required for administrative, maintenance, and support per participant per week (excludes 1st visit)

Secondary Outcome Measures

Acceptability: Participant Retention
Percentage of individuals who enrolled and completed the study at 6 months
Acceptability: System Usability Score
Ten-items, Likert scale (1-5), 1 is strongly disagree and 5 is strongly agree To calculate the System Usability Score (SUS), first sum the score contributions from each item. Each item's score contribution will range from 0 to 4. For items 1,3,5,7,and 9 the score contribution is the scale position minus 1. For items 2,4,6,8 and 10, the contribution is 5 minus the scale position. Multiply the sum of the scores by 2.5 to obtain the overall value of System Usability (SU). SUS scores have a range of 0 to 100.
Acceptability: Satisfaction Acceptability Questionnaire
Measure participant satisfaction with intervention delivered via mobile application at 6-months using a 30-item questionnaire (1 Excellent-6 Unsatisfied) administered through an online survey. An average score greater than or equal to 144 (80%) will be considered acceptable.

Full Information

First Posted
April 29, 2018
Last Updated
June 28, 2022
Sponsor
University of California, San Francisco
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT03587857
Brief Title
mHealth App for Engagement in Care Among Youth Living With HIV
Official Title
A Mobile Health Application for Engagement in Care Among Youth Living With HIV
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
May 1, 2020 (Actual)
Study Completion Date
May 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In the US, fewer than 6% of all youth living with HIV (YLWH) achieve HIV viral suppression. However, health disparities among youth extend across the entire HIV care continuum in that there is a strong association between younger age and later HIV diagnosis, lower engagement in care, lower levels of antiretroviral therapy (ART) adherence, and worse HIV clinical outcomes. In response to this critical public health dilemma, the investigators propose to develop a novel mobile health application ("app") to improve engagement in health care and ART adherence and to pilot test this mobile health app in 18-29-year-old YLWH residing in San Francisco. The aims of this study are to: Aim 1: Build on a theory-guided model and formative work to complete the development of a novel personalized mobile health app for improved HIV clinical outcomes among YLWH (includes field test of initial release to ensure adequate usability and engagement). Aim 2: Conduct a six-month single arm pilot study to examine WYZ feasibility and acceptability among YLWH ( N = 76) living in the San Francisco Bay Area. Finally, the investigators will conduct in-depth qualitative interviews with a subset of participants (N = 20) and clinical team members (N = 10) whose patients participated in the pilot study. The investigators hypothesize that this mobile health app will be feasible and acceptable and will result in improved HIV clinical outcomes. Upon completion, the investigators will be ready to test the efficacy of this app in a subsequent large-scale randomized control trial among a population that is disproportionately impacted by HIV and at elevated risk for poor clinical outcomes.
Detailed Description
WYZ is a modular, adaptive, and personalized intervention delivered via a mobile phone. It is grounded in the Information-Motivation-Behavioral Skills (IMB) model which has been valuable for understanding and guiding the development of interventions for complex health behaviors. WYZ was created in collaboration with 18-29 year-old YLWH using a Human-Centered Design (HCD) approach that emphasizes understanding the perspective of the users of the technology. WYZ is intended to improve engagement in HIV care by 1) enhancing medication adherence self-efficacy, 2) increasing awareness and use of community resources, 3) reducing barriers to communication between youth and their healthcare team, and 4) providing a secure platform for the formation of a supportive closed online community of YLWH. The investigators will complete development of WYZ (1.0), field test the initial release with a cohort of 10 potential users over a period of three months to identify and address technical challenges, and develop a fully functioning version (WYZ 2.0) that can be used in a pilot investigation. The investigators will then conduct a six-month single-arm pilot study to examine WYZ feasibility and acceptability among (N = 76) YLWH (18-29 years old) who live and/or receive care in the San Francisco Bay Area. The objectives of this forthcoming phase are to refine the design so as to improve satisfaction and engagement with the intervention among YLWH and their healthcare providers. The main outcomes of the pilot trial include feasibility and acceptability as indicated by meeting or exceeding proposed benchmarks. Feasibility will be assessed via user metrics by examining the participant's interactions with WYZ via a mobile analytics service called Flurry and backend (Salesforce) reporting tools. Acceptability will be examined during regular phone check-ins, a system usability scale (SUS), a satisfaction survey, and an exit qualitative interview. In addition to feasibility measures, the investigators will calculate an engagement index (EI) for each participant. The EI has been detailed and used successfully in other mHealth interventions. The EI includes the following sub-indices: (1) click depth (number of pages a user views per session), (2) loyalty (measures how frequently users access the application during the study period), (3) recency (the time difference between each session the user accessed the application), (4) interaction (number of push notifications opened from those sent through the application), and (5) feedback (subjective measure of participants' satisfaction with the application). Based on the data from participants in this pilot study, the investigators will develop a refined version of WYZ (3.0), which will be used in a future investigation to examine the efficacy of the intervention with a much larger sample.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV/AIDS, Mobile Health, Young Adults
Keywords
Health Disparity

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
83 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1: Intervention
Arm Type
Experimental
Arm Description
All YLWH who choose to enroll in the study will receive access to WYZ, the mobile health application. The participants will be asked to use the app for 6 months, during which the investigators will assess the feasibility and acceptability of WYZ. Based on this initial data, the investigators will refine and release a new version of the app (WYZ 3.0).
Intervention Type
Other
Intervention Name(s)
Mobile Health Application
Other Intervention Name(s)
WYZ
Intervention Description
This mobile health app is a modular, adaptive, and personalized intervention delivered via a mobile phone. It is grounded in the Information Motivation Behavioral Skills (IMB) model. It was created in collaboration with YLWH (18-29 years-old) using a Human-Centered Design approach to help improve engagement in HIV care among this age group.
Primary Outcome Measure Information:
Title
Feasibility: Rate of Participant Recruitment
Description
Recruit at least 55 participants (i.e. 70% of target N)
Time Frame
8 Months
Title
Feasibility: Frequency of WYZ Access
Description
Percentage of participants who achieve an average of 1 log-in per week
Time Frame
Baseline to 6 Months
Title
Feasibility: Length of Session (Minutes)
Description
Percentage of participants who achieve an average of 15 minutes in application per week
Time Frame
Baseline To 6 Months
Title
Feasibility: Rate of Use of Refill Reminders
Description
Percentage of participants that use feature once monthly (if receiving 30-day ART supply)
Time Frame
Baseline To 6 Months
Title
Feasibility: Rate of Use of ART Adherence Tracking
Description
Percentage of participants that track med adherence at least 3 times per week
Time Frame
Baseline To 6 Months
Title
Feasibility: Rate of Access of Laboratory Data
Description
Percentage of participants that review laboratory data at least one-time per month
Time Frame
Baseline To 6 Months
Title
Feasibility: Rate of Communication With Clinical Team Members
Description
Percentage of participants who achieve an average of 1 communication exchange per month with clinical team member
Time Frame
Baseline To 6 Months
Title
Feasibility: Rate of Communication With Peers
Description
Percentage of participants who achieve an average of one post or response to a post per week
Time Frame
Baseline To 6 Months
Title
Feasibility: Rate of Access of Health News
Description
Percentage of participants who review health news at least once per week
Time Frame
Baseline To 6 Months
Title
Feasibility: Rate of Access of Event Calendar
Description
Percentage of participants who review event calendar at least once per week
Time Frame
Baseline To 6 Months
Title
Feasibility: Time For Participant Onboarding (Minutes)
Description
Average time to onboard new participant (including downloading app and reviewing app features)
Time Frame
Baseline To 6 Months
Title
Feasibility: Time To Maintain & Support (Minutes)
Description
Average time required for administrative, maintenance, and support per participant per week (excludes 1st visit)
Time Frame
Baseline To 6 Months
Secondary Outcome Measure Information:
Title
Acceptability: Participant Retention
Description
Percentage of individuals who enrolled and completed the study at 6 months
Time Frame
Baseline To 6 Months
Title
Acceptability: System Usability Score
Description
Ten-items, Likert scale (1-5), 1 is strongly disagree and 5 is strongly agree To calculate the System Usability Score (SUS), first sum the score contributions from each item. Each item's score contribution will range from 0 to 4. For items 1,3,5,7,and 9 the score contribution is the scale position minus 1. For items 2,4,6,8 and 10, the contribution is 5 minus the scale position. Multiply the sum of the scores by 2.5 to obtain the overall value of System Usability (SU). SUS scores have a range of 0 to 100.
Time Frame
Baseline To 6 Months
Title
Acceptability: Satisfaction Acceptability Questionnaire
Description
Measure participant satisfaction with intervention delivered via mobile application at 6-months using a 30-item questionnaire (1 Excellent-6 Unsatisfied) administered through an online survey. An average score greater than or equal to 144 (80%) will be considered acceptable.
Time Frame
Baseline To 6 Months
Other Pre-specified Outcome Measures:
Title
Mobile Application Engagement Index (EI)
Description
The engagement index (EI) measures overall engagement with the app. The score is calculated by adding scores for 5 sub-indices: (1) click depth (number of pages viewed per session), (2) loyalty (frequency of application access), (3) recency (time between each session), (4) interaction (number of notifications opened), (5) feedback (participant's satisfaction with the application). The final score incorporated click depth, loyalty, recency, interaction, and feedback sub-indices. Equal weight was assigned for each of the sub-index. Four of the sub-indices were calculated using app data. The feedback index was informed using responses to the 6-month satisfaction survey. The EI was then converted to a value between 0 and 100. Cut-off points were developed based on the distribution of the total samples' EI scores using quartiles. Participants were then categorized as either poorly, moderately, or highly engaged.
Time Frame
Baseline To 6 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
29 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Eligibility Criteria: Must be between 18 and 29 years of age Must be living with HIV Must reside and/or get care in San Francisco Bay Area Must be able to provide informed consent to be a research participant Must be able to speak and understand English Must have access to an Android (5.0 or higher) or iOS (10.0 or higher) mobile phone Exclusion Criteria: Evidence of cognitive impairment or psychotic disorder that prevents one from understanding the purpose of the study and/or participating fully in study activities. This determination will be made by trained study staff in consultation with the principal investigator.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Parya Saberi, PhamD
Organizational Affiliation
UCSF School of Medicine, Division of Prevention Science
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California San Francisco, Mission Bay Campus
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31061063
Citation
Erguera XA, Johnson MO, Neilands TB, Ruel T, Berrean B, Thomas S, Saberi P. WYZ: a pilot study protocol for designing and developing a mobile health application for engagement in HIV care and medication adherence in youth and young adults living with HIV. BMJ Open. 2019 May 5;9(5):e030473. doi: 10.1136/bmjopen-2019-030473.
Results Reference
background
PubMed Identifier
34463622
Citation
Saberi P, Lisha NE, Erguera XA, Hudes ES, Johnson MO, Ruel T, Neilands TB. A Mobile Health App (WYZ) for Engagement in Care and Antiretroviral Therapy Adherence Among Youth and Young Adults Living With HIV: Single-Arm Pilot Intervention Study. JMIR Form Res. 2021 Aug 31;5(8):e26861. doi: 10.2196/26861.
Results Reference
result
PubMed Identifier
33920803
Citation
Lisha NE, Neilands TB, Erguera XA, Saberi P. Development of the Mobile Technology Vulnerability Scale among Youth and Young Adults Living with HIV. Int J Environ Res Public Health. 2021 Apr 15;18(8):4170. doi: 10.3390/ijerph18084170.
Results Reference
result

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mHealth App for Engagement in Care Among Youth Living With HIV

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