Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05412212 · ClinicalTrials.gov registry record · NA

Brief Educational Video for Patients Prescribed LTBI Treatment

A NA study of Latent Tuberculosis, sponsored by Kaiser Permanente.

Active
Registry status
NA
Development phase
1,898
Enrollment target
1
Study location

NCT05412212: Active NA study of Latent Tuberculosis, sponsored by Kaiser Permanente.

NCT05412212 is a NA study of Latent Tuberculosis that is active but no longer recruiting, run by Kaiser Permanente. The registered enrollment target is 1,898 participants, above the 826-participant average among 5 other Latent Tuberculosis trials with a reported enrollment target (130% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05412212, a NA study of Latent Tuberculosis, is active but no longer recruiting, sponsored by Kaiser Permanente.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
1,898 participants
Enrollment target
1
Study location

Study Summary

Many patients who are prescribed treatment for latent tuberculosis (LTBI) do not complete treatment. Effective interventions that are low-cost and feasible for large-scale implementation are needed to support efforts to eliminate TB. The investigators hypothesize that a 3-minute educational LTBI video intervention will improve treatment completion compared to standard care (no intervention). A randomized trial will be conducted at Kaiser Permanente Southern California, including adults who are prescribed treatment for LTBI, identified using an electronic health record algorithm. At the time of treatment prescription, patients will be randomized to receive the LTBI video intervention or standard care at a ratio of 2 to 1. Those in the intervention group will be sent a secure text message or e-mail with a link to the video. Individuals who watch the LTBI video will be invited to respond to 4 short questions about their perceptions of the video accessibility and content. The primary outcome is LTBI treatment completion (dispensation of the required number of doses) in the year following prescription order. Secondary outcomes are LTBI treatment initiation (at least one dispensation) in the year following prescription order; initiation and completion within the year following prescription order stratified by LTBI treatment regimen (if feasible); the proportion of individuals randomized to the intervention group who watched the LTBI video; and the perceptions of those who watched the video. The primary analysis will be based on intention-to-treat. Characteristics of individuals in the intervention and standard care groups will be described, and rates of LTBI treatment completion will be calculated. To assess the effect of the intervention, Poisson regression with robust standard errors will be used to estimate unadjusted and adjusted rate ratios and 95% confidence intervals. Per-protocol analyses will also be conducted, comparing those in the intervention group who wat

Primary Outcome

Proportion of patients prescribed LTBI treatment who complete the treatment within one year of treatment prescription

Conditions Studied

Interventions

  • OTHER LTBI video intervention

Study Locations (1)

California

  • Kaiser Permanente Southern California Department of Research and Evaluation - Pasadena

Trial Details

FieldValue
Enrollment Target 1,898 participants
Start Date 2022-06-03
Est. Completion 2025-12-31
Phase NA
Kaiser Permanente

294 total trials

What the registry record for NCT05412212 still lists

NCT05412212 is an interventional study that assigns participants to a tested intervention. Its 1,898 participants enrollment target places it among the larger protocols in the corpus, above the 826-participant average among 5 other Latent Tuberculosis trials with a reported enrollment target (130% higher).

The record links to 1 condition, with Latent Tuberculosis appearing as the primary indexed condition, and to 1 intervention - of which LTBI video intervention is the first listed.

NCT05412212 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT05412212 about?

NCT05412212 is a clinical study titled "Brief Educational Video for Patients Prescribed LTBI Treatment". Many patients who are prescribed treatment for latent tuberculosis (LTBI) do not complete treatment. Effective interventions that are low-cost and feasible for large-scale implementation are needed to support efforts to eliminate TB. The investigators hypothesize that a 3-minute educational LTBI vid...

What is the current status of trial NCT05412212?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 1,898 participants. The study started on 2022-06-03. Estimated completion is 2025-12-31.

What conditions does trial NCT05412212 study?

This clinical trial studies the following conditions: Latent Tuberculosis.

What interventions are being tested in trial NCT05412212?

The interventions under investigation include: LTBI video intervention (OTHER).

Who is sponsoring clinical trial NCT05412212?

This trial is sponsored by Kaiser Permanente, which has 294 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05412212 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Latent Tuberculosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03729180 · 1,900 participants · NA

    The ImPreSS Trial: Pharmacogenomic Decision Making at Time of Surgery

  • NCT05712200 · 1,900 participants · Phase 3

    Study to evaLuate the effIcacy and Safety of abeLacimab in High-risk Patients With Atrial Fibrillation Who Have Been Deemed Unsuitable for Oral antiCoagulation (LILAC-TIMI 76)

  • NCT06929806 · 1,900 participants · Phase 3

    Multi-center Trial of Ferric Derisomaltose Versus no Intravenous Iron in Iron-deficient Subjects With Symptomatic Chronic Heart Failure

  • NCT07228234 · 1,900 participants · NA

    Evaluating Mammography Communication Approaches

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05412212, the US trial registry maintained by the National Library of Medicine. NCT05412212 (large enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.