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SmartSteps: A Context-Aware, PrEP Adherence Intervention for Individuals With Substance Use Disorder (SmartSteps)

Primary Purpose

HIV Infections, Substance Use, Adherence, Medication

Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Descovy or Truvada
ID-Cap System
Beiwe
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring Pre-Exposure Prophylaxis, Substance Use, Digital Pill System, Adherence, HIV Prevention

Eligibility Criteria

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

Inclusion Criteria:

  1. Age 18 or older
  2. Cisgender male
  3. Has sex with men
  4. HIV negative
  5. On PrEP or initiating PrEP (including switching from 2-1-1 or "on-demand" PrEP dosing to once-daily dosing)
  6. Moderate risk score on ASSIST substance use screener (11-26 for alcohol, 4-26 for all other substances) or higher
  7. Qualifying laboratory testing for PrEP: Cr clearance in past 3 months, HBV vaccination, liver function tests
  8. Owns a smartphone with Android or iOS

Exclusion Criteria:

  1. Does not speak English
  2. History of Crohn's disease or ulcerative colitis
  3. History of gastric bypass or bowel stricture
  4. History of GI malignancy or radiation to abdomen
  5. Allergy to gelatin, silver, or zinc (components of digital pill)
  6. Allergy to PrEP
  7. Not willing to operate DPS or Beiwe app

Sites / Locations

  • Fenway HealthRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Digital Pills and Beiwe

Arm Description

Participants will take one PrEP digital pill per day, for 60 days total, while using the ID-Cap digital pill system and Beiwe digital phenotyping app.

Outcomes

Primary Outcome Measures

PrEP Adherence Patterns
Percentage adherence to PrEP and adherence patterns over the course of 60 days, as detected by the ID-Cap digital pill system (DPS).
Correlation of PrEP Adherence with Digital Phenotyping Patterns
Comparison of digital phenotyping data, as detected by Beiwe, on PrEP-adherent versus PrEP-nonadherent days, as detected by the digital pill system (DPS).

Secondary Outcome Measures

Correlation of PrEP Adherence with DBS Concentrations
Correlation of PrEP adherence patterns, as detected by the digital pill system (DPS), with tenofovir diphosphate concentrations in dried blood spots (DBS).
Acceptability of DPS and Digital Phenotyping App
User acceptance of and willingness to interact with the digital pill system (DPS) and Beiwe digital phenotyping app, as assessed via qualitative exit interviews.

Full Information

First Posted
May 12, 2022
Last Updated
December 20, 2022
Sponsor
Brigham and Women's Hospital
Collaborators
Gilead Sciences, The Fenway Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05378399
Brief Title
SmartSteps: A Context-Aware, PrEP Adherence Intervention for Individuals With Substance Use Disorder
Acronym
SmartSteps
Official Title
SmartSteps: A Context-Aware, Pre-Exposure Prophylaxis Adherence Intervention for Individuals With Substance Use Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 20, 2022 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
August 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
Gilead Sciences, The Fenway Institute

4. Oversight

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

5. Study Description

Brief Summary
This is a single-arm, observational study of HIV-negative MSM with substance use disorder. Those who meet pre-screening criteria will attend a Screening Visit (Visit 1), where the informed consent process will be conducted and study eligibility will be confirmed. Eligible participants will attend three additional visits over the course of the study - the Enrollment Visit (Visit 2), Month 1 Visit (Visit 3), and Month 2 Visit (Visit 4). Participants will take one PrEP digital pill per day, for 60 days total, while using the digital pill system (DPS) and Beiwe, a digital phenotyping app. On nonadherent days, participants will receive brief surveys prompting them to report the reasons for their missed dose, as well as their engagement in substance use and sexual activity. Timeline followback will be conducted at the Month 1 and Month 2 Visits to understand the context of any nonadherence. Qualitative user experience exit interviews and dried blood spots (DBS) will be conducted at the Month 2 Visit.
Detailed Description
This study will develop a dataset of annotated smartphone usage in the context of PrEP adherence and nonadherence. In order to understand smartphone context, the investigators will utilize a digital pill system (DPS) to measure real-time PrEP ingestion events. Eligibility will be confirmed during the Screening Visit (Visit 1). During the Enrollment Visit (Visit 2), participants will complete a baseline quantitative assessment (e.g., sociodemographics, sexual history, attitudes about technology), receive training on the operation of the DPS and Beiwe, and will ingest their first digital pill dose under observation by study staff. Participants will be instructed to take one PrEP pill once daily while using the DPS and Beiwe app for 60 days. Participants will return for a study visit at the end of month one (Visit 3) for a refill of digital pills. Following a 24-hour period which no PrEP ingestion is detected by the DPS, participants will receive a brief online substance use and sexual risk survey, which will inform specific contexts of nonadherence. At the Month 1 Visit (Visit 3) and Month 2 Visit (Visit 4), timeline followback discussions will be conducted to better understand the context of any PrEP nonadherence events detected by the DPS, and phenotypic data collected by the Beiwe app, during the prior 30 days. At the Month 2 (Visit 4), the investigators will administer a blood draw for dried blood spot (DBS) testing to measure participants' PrEP adherence and compare it against adherence detected by the DPS. To gain insight into user experiences operating the DPS and Beiwe app as part of the study, the investigators will conduct the semi-structured qualitative exit interviews with participants at Month 2 (Visit 4).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Substance Use, Adherence, Medication, Adherence, Treatment
Keywords
Pre-Exposure Prophylaxis, Substance Use, Digital Pill System, Adherence, HIV Prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Digital Pills and Beiwe
Arm Type
Experimental
Arm Description
Participants will take one PrEP digital pill per day, for 60 days total, while using the ID-Cap digital pill system and Beiwe digital phenotyping app.
Intervention Type
Drug
Intervention Name(s)
Descovy or Truvada
Intervention Description
Descovy or Truvada prescribed with digital pills for PrEP
Intervention Type
Device
Intervention Name(s)
ID-Cap System
Other Intervention Name(s)
digital pill
Intervention Description
Digital pills overencapsulating Descovy or Truvada for PrEP
Intervention Type
Device
Intervention Name(s)
Beiwe
Intervention Description
Digital phenotyping app
Primary Outcome Measure Information:
Title
PrEP Adherence Patterns
Description
Percentage adherence to PrEP and adherence patterns over the course of 60 days, as detected by the ID-Cap digital pill system (DPS).
Time Frame
After Month 2 Visit
Title
Correlation of PrEP Adherence with Digital Phenotyping Patterns
Description
Comparison of digital phenotyping data, as detected by Beiwe, on PrEP-adherent versus PrEP-nonadherent days, as detected by the digital pill system (DPS).
Time Frame
After Month 2 Visit
Secondary Outcome Measure Information:
Title
Correlation of PrEP Adherence with DBS Concentrations
Description
Correlation of PrEP adherence patterns, as detected by the digital pill system (DPS), with tenofovir diphosphate concentrations in dried blood spots (DBS).
Time Frame
After Month 2 Visit
Title
Acceptability of DPS and Digital Phenotyping App
Description
User acceptance of and willingness to interact with the digital pill system (DPS) and Beiwe digital phenotyping app, as assessed via qualitative exit interviews.
Time Frame
After Month 2 Visit

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Cisgender men who have sex with men
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 or older Cisgender male Has sex with men HIV negative On PrEP or initiating PrEP (including switching from 2-1-1 or "on-demand" PrEP dosing to once-daily dosing) Moderate risk score on ASSIST substance use screener (11-26 for alcohol, 4-26 for all other substances) or higher Qualifying laboratory testing for PrEP: Cr clearance in past 3 months, HBV vaccination, liver function tests Owns a smartphone with Android or iOS Exclusion Criteria: Does not speak English History of Crohn's disease or ulcerative colitis History of gastric bypass or bowel stricture History of GI malignancy or radiation to abdomen Allergy to gelatin, silver, or zinc (components of digital pill) Allergy to PrEP Not willing to operate DPS or Beiwe app
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Peter R Chai, MD MMS
Phone
617-732-5640
Email
pchai@fenwayhealth.org
First Name & Middle Initial & Last Name or Official Title & Degree
Georgia Goodman, BS
Phone
857-301-8820
Email
ggoodman@fenwayhealth.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter R Chai, MD MMS
Organizational Affiliation
Brigham and Women's Hopsital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fenway Health
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peter R Chai, MD, MMS
Phone
617-732-5640
Email
pchai@bwh.harvard.edu
First Name & Middle Initial & Last Name & Degree
Georgia Goodman, BS
Phone
857-301-8820
Email
ggoodman@fenwayhealth.org

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

SmartSteps: A Context-Aware, PrEP Adherence Intervention for Individuals With Substance Use Disorder

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