DOT Diary Optimization Pilot: A Pilot Study to Optimize the DOT Diary App to Measure PrEP Adherence

Public Health Foundation Enterprises, Inc.

Status and phase

Completed

Phase 4

Conditions

Pre-Exposure Prophylaxis

Risk Behavior

Adherence, Medication

HIV Prevention

Treatments

Other: DOT Diary mobile app

Drug: Emtricitabine / Tenofovir Disoproxil Oral Tablet

Study type

Interventional

Funder types

Other

Industry

NIH

Identifiers

NCT03387462

17-22864

1R01MH109320-01 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The researchers are working with a technology company, AiCure, to develop a smartphone app, DOT Diary, which combines two drug adherence strategies. DOT Diary reminds people when it is time to take their medication, and uses motion-sensing technology to visually and automatically confirm the pill was swallowed. The goal of this study is to understand people's experiences using this new app while taking HIV pre-exposure prophylaxis (PrEP) for the prevention of HIV.

Full description

In the DOT Diary research project, the AiCure aDOT smartphone app has been adapted for use in monitoring and supporting HIV pre-exposure prophylaxis (PrEP) use among young men who have sex with men (YMSM). The aDOT app uses automated directly observed therapy (DOT) that use the smartphone camera and artificial intelligence software to confirm that the right person is taking the right medication at the right time. A sexual diary has been integrated into the aDOT app to assist YMSM in understanding whether they are receiving protection from PrEP for individual sexual episodes, and when it is particularly important to take PrEP (e.g. after a sexual episode).

In the next stage of app development, the researchers are conducting this study to identify areas of the app that require refinement to maximize the acceptability and ease of use of the DOT adherence monitoring app. The researchers will assess overall acceptability and ease of use of the integrated DOT Diary (D2) app over an 8 week period.The goal of this pilot study will be to refine and optimize the app for further testing in a larger and longer pilot study among YMSM at risk for HIV acquisition. The researchers will conduct this pilot protocol among YMSM in Atlanta and San Francisco Bay Area, two metropolitan regions heavily impacted by HIV, yet differing in sociodemographics, as well as in the availability and uptake of HIV prevention services, including PrEP. These diverse research locations will allow collection of data to inform app development among a broad group of YMSM.

Enrollment

20 patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Self-identifies as a man
Age 18-35 at enrollment
Reports having anal sex with a man or trans woman in the past 12 months and one or more of the following criteria in the past 12 months:
- Any condomless anal sex (not in a mutually monogamous relationship with an HIV-negative partner)
- Two or more anal sex partners
- Self-reported STI (gonorrhea, chlamydia, syphilis)
- Having a known HIV-positive sexual partner
HIV-negative as determined by a negative 4th generation HIV test at screening and negative rapid 4th generation test at enrollment
Currently taking PrEP or interested in initiating PrEP
Eligible to take PrEP
- Creatinine clearance ≥60 ml/min as estimated by Cockcroft-Gault equation at screening
- Hepatitis B surface antigen (HBsAg) negative
Willing and able to provide written informed consent
Able to read and speak English
Smartphone ownership compatible with DOT Diary
Meets local locator requirements

Exclusion criteria

Any reactive HIV test at screening or enrollment
Signs or symptoms of acute HIV infection at screening or enrollment
History of pathological bone fracture not related to trauma
Taking nephrotoxic medications
History of participation in the active arm of an HIV vaccine trial
In a mutually monogamous sexual relationship with an HIV-negative partner for the past 12 months
Does not live, work or play in Atlanta Metropolitan Area, San Francisco, Alameda, Marin, Contra Costa, Santa Clara, or San Mateo Counties
Unable to commit to study participation for 8 weeks
Any medical, psychiatric, or social condition or other responsibilities that, in the judgment of the investigator, would make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.