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Clinical Practice Guidelines Versus Decision-support for Latent Tuberculosis Infection (LTBI) Management

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Johns Hopkins University

Status

Completed

Conditions

Latent Tuberculosis

Treatments

Behavioral: CDC/NTCA guidelines only
Behavioral: LTBI ASSIST and CDC/NTCA guidelines only

Study type

Interventional

Funder types

Other

Identifiers

NCT05772065
IRB00376488

Details and patient eligibility

About

Latent Tuberculosis infection (LTBI) guidelines can be complex. LTBI-ASSIST is a web-based interactive tool to navigate US LTBI clinical practice guidelines in a patient-centered format that may guide clinical decision making around Latent TB care.

The research goal is to determine the difference in reported confidence among trainees that are not experts in LTBI care. The investigators further aim to assess if access to the LTBI-ASSIST tool improves clinical decision making in a series of simulated case scenarios containing guideline-derived, multiple choice items, as well as assess the efficiency in navigating the scenarios - measured by time to complete the survey.

The investigators proposed a randomized study design, in which an electronic survey/questionnaire with 4 case scenarios consisting of 14 multiple choice questions. Participants providing informed consent will be randomized to receiving access to either US Centers for Disease Control (CDC)/National Tuberculosis (TB) Controllers Association (NTCA) Guidelines or the LTBI-ASSIST online tool. Those in the experimental arm will further complete a 10 question System Usability Scale to assess usability of the LTBI-ASSIST tool.

All Johns Hopkins medical trainees and residents will be eligible to participate.

Enrollment

168 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Student at Johns Hopkins School of Medicine, or Medical trainee at Hopkins Hospital or Bayview Program

Exclusion criteria

  • None

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

168 participants in 2 patient groups

CDC/NTCA guidelines only
Active Comparator group
Description:
The control group will have a link to US guidelines only and use it as a resource to answer the case vignettes.
Treatment:
Behavioral: CDC/NTCA guidelines only
LTBI ASSIST and CDC/NTCA guidelines
Experimental group
Description:
The intervention group will have a link to both US guidelines, and the LTBI-ASSIST tool as resources to answer the case vignettes.
Treatment:
Behavioral: LTBI ASSIST and CDC/NTCA guidelines only

Trial contacts and locations

1

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Central trial contact

Samuel Starke, MD; Maunank Shah, MD, PhD

Data sourced from clinicaltrials.gov

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