Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03387462
Other study ID # 17-22864
Secondary ID 1R01MH109320-01
Status Completed
Phase Phase 4
First received
Last updated
Start date February 28, 2018
Est. completion date August 30, 2018

Study information

Verified date October 2021
Source Public Health Foundation Enterprises, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 30, 2018
Est. primary completion date August 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility 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.

Study Design


Intervention

Drug:
Emtricitabine / Tenofovir Disoproxil Oral Tablet
Open label daily emtricitabine/tenofovir disoproxil oral tablet
Other:
DOT Diary mobile app
DOT Diary mobile application for tracking medication adherence and sexual activities.

Locations

Country Name City State
United States Emory University, School of Public Health Atlanta Georgia
United States Bridge HIV, San Francisco Department of Public Health San Francisco California

Sponsors (5)

Lead Sponsor Collaborator
Public Health Foundation Enterprises, Inc. AiCure, Emory University, National Institute of Mental Health (NIMH), San Francisco Department of Public Health

Country where clinical trial is conducted

United States, 

References & Publications (1)

Liu AY, Laborde ND, Coleman K, Vittinghoff E, Gonzalez R, Wilde G, Thorne AL, Ikeguchi E, Shafner L, Sunshine L, van der Straten A, Siegler AJ, Buchbinder S. DOT Diary: Developing a Novel Mobile App Using Artificial Intelligence and an Electronic Sexual D — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary DOT Diary Mobile App Acceptability System Usability Scale (SUS) is a 10 item questionnaire with 5 response options: strongly disagree to strongly agree. These are scored 0-4. The scores are then summed up (making sure all positive responses -- increased usability -- are given the higher scores). The final score is multiplied by 2.5 Possible scores are from 0-100, with maximal usability achieving the higher score. Although the scores are 0-100, these are not percentages and should be considered only in terms of their percentile ranking. 8 weeks
Primary DOT Diary Mobile App Ease of Use 5-point Likert scale (1=strongly disagree that app is easy to use; 5=strongly agree that app is easy to use) on a single question of the key attribute of ease of use of DOT Diary over 8 weeks by MSM on PrEP. 8 weeks
Primary Adherence and Persistence of Use of the DOT and Sexual Diary Components of DOT Diary by Young MSM on PrEP Adherence and Persistence of use of the DOT and sexual diary components of DOT Diary by young MSM on PrEP is measured by the percentage of doses taken with visual confirmation of pill ingestion 8 weeks
Secondary Assessment of Situations and Reasons for Sub-optimal Use of the App Combined analysis of situations and reasons for sub-optimal use of the app, for the purpose of app optimization 8 weeks
See also
  Status Clinical Trial Phase
Completed NCT03411577 - Development and Testing of a Jamaican Mother-daughter HIV Risk-reduction Program N/A
Active, not recruiting NCT03112369 - Preventing HIV Among Native Americans Through the Treatment PTSD & Substance Use N/A
Not yet recruiting NCT03642314 - HIV Self-testing in Implementation PrEP Study N/A
Completed NCT01810315 - Influence of Reproductive Cycle and Menopause on HIV-1 Infection and TFV Gel Activity Phase 1
Completed NCT00984971 - Rectal Microbicide Safety and Acceptability Trial of Topically Applied Tenofovir Compared With Oral Tablet Phase 1
Completed NCT00142935 - Effectiveness of Opiate Replacement Therapy Administered Prior to Release From a Correctional Facility - 1 N/A
Active, not recruiting NCT03255915 - PrEP-Pod-IVR (TDF-FTC/Placebo IVR 28 Day Crossover Study) Early Phase 1
Completed NCT05037513 - Integrated PrEP Interventions for People Who Inject Drugs in Rural Kentucky N/A
Recruiting NCT05087680 - An Acceptance Based PrEP Intervention to Engage Young Black MSM in the South N/A
Recruiting NCT05804461 - Optimizing Pre-Exposure Prophylaxis (PrEP) Among Latino Men Who Have Sex With Men (MSM) in Puerto Rico N/A
Completed NCT03148171 - Project WERK (Wellness Encouragement Respect Kinship) N/A
Completed NCT04791007 - OB-002H Gel Administered Vaginally and Rectally in HIV-1 Seronegative Adults Early Phase 1
Recruiting NCT05412433 - Clinic-based HIV Identification and Prevention Project Using Electronic Resources N/A
Active, not recruiting NCT03977181 - The Community PrEP Study to Assess the Acceptance of PrEP Delivered Through CBCT Platforms N/A
Recruiting NCT05165745 - Stick2PrEP Cisgender Women and Trans Individuals N/A
Completed NCT03719053 - Single Dose Truvada Study Phase 1
Recruiting NCT03856580 - Long-acting Biomedical HIV Prevention in Transgender Women N/A
Completed NCT02750540 - Optimization of a Tenofovir Enema for HIV Prevention Phase 1
Completed NCT01386294 - Safety and Effectiveness of Tenofovir Gel in the Prevention of Human Immunodeficiency Virus (HIV-1) Infection in Women and the Effects of Tenofovir Gel on the Incidence of Herpes Simplex Virus (HSV-2) Infection Phase 3
Completed NCT00993811 - The Shang Ring: A Novel Male Circumcision Device for HIV Prevention Phase 1