Actively Recruiting
Economic Incentives and Video Directly Observed Therapy to Promote Adherence to Latent Tuberculosis Infection
Led by Johns Hopkins University · Updated on 2026-05-04
399
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
Sponsors
J
Johns Hopkins University
Lead Sponsor
N
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating a new approach combining Video Directly Observed Therapy (vDOT) and financial incentives to help adults complete treatment for latent tuberculosis (TB). The study focuses on adults starting treatment for latent TB in the Baltimore area, aiming to increase treatment completion rates compared to usual care. This is an interventional trial designed to address challenges like poverty, access to care, and language barriers that often affect treatment adherence in this population. Participants will be randomly assigned to one of three groups: usual care with medication and nurse case management, Video-DOT using a smartphone app to record medication intake, or Video-DOT plus financial incentives for verified medication adherence. The Video-DOT system uses the emocha app to securely record and confirm medication ingestion, while the incentive group can earn payments based on their adherence. Medication regimens include short courses with isoniazid, rifapentine, or rifampin, and treatment lasts up to six months. During the study, participants will have their medication adherence monitored through electronic caps on medication bottles and video verification. Researchers will assess treatment completion, defined as taking at least 80% of prescribed doses, along with other adherence measures and the costs of the incentive program. Visits will include routine care, education, and toxicity assessments. The study runs for up to six months with extended cost-effectiveness follow-up for five years, ensuring careful monitoring and support throughout treatment.
CONDITIONS
Brief Title
Economic Incentives and vDOT for Latent Tuberculosis Infection
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years old or older
- Diagnosed with latent tuberculosis and prescribed treatment by a clinician
- Reside in the Baltimore metropolitan area
- Speak English, Spanish, or a language with a Johns Hopkins consent form available
- Prescribed 3 months of Isoniazid/Rifapentine, 3 months of Isoniazid/Rifampin, or 4 months of Rifampin
You will not qualify if you...
- Younger than 18 years old
- Diagnosed with active tuberculosis
- Prescribed a different treatment regimen for latent tuberculosis
- Pregnant women (confirmed by clinical evaluation)
- Participant's spoken language does not have an available translated consent form
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 6 months
Participants take prescribed medication for latent tuberculosis infection with adherence monitored either by usual care, video directly observed therapy, or video therapy plus financial incentives.
Visits to receive medication dispensed in 30-60 day supplies; video submissions for medication ingestion as applicable
Trial Site Locations
Total: 1 location
1
Baltimore City Health Department, and Baltimore metropolitan area clinics and health departments
Baltimore, Maryland, United States, 21205
Actively Recruiting
Research Team
P
Principal Investigator
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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