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

NCT03834350 · ClinicalTrials.gov registry record · NA

At Home Spirometry and Video Module Education for COPD Patients

A NA study of COPD, sponsored by University of Chicago.

Completed
Registry status
NA
Development phase
71
Enrollment target
1
Study location

NCT03834350: Completed NA study of COPD, sponsored by University of Chicago.

NCT03834350 is a NA study of COPD that has completed, run by University of Chicago. The registered enrollment target is 71 participants, below the 2,418-participant average among 85 other COPD trials with a reported enrollment target (97% lower). 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

NCT03834350, a NA study of COPD, has completed, sponsored by University of Chicago.

COMPLETED
Registry status
NA
Development phase
71 participants
Enrollment target
1
Study location

Study Summary

The central hypothesis is that patients hospitalized for COPD who subsequently complete the at-home BREATHES Program with V-TTG skill training and SpiroPD adherence support will retain increased medication knowledge, skill, self-efficacy, and adherence that otherwise decays substantially by 30 days post-discharge. To test this hypothesis, this study proposes the following specific aims: Aim 1: Determine the feasibility of, adherence to, and efficacy of at-home V-TTG for ongoing inhaler skill training. Hypothesis: Participants who complete both in-hospital and at-home V-TTG will have a significantly increased likelihood of demonstrating effective respiratory inhaler technique within 30 days after hospital discharge compared to in-hospital technique Aim 2. Determine the feasibility of, adherence to, and efficacy of at-home SpiroPD for COPD medication adherence support. Hypothesis: Participants' use of SpiroPD (PMD Healthcare) will significantly improve their COPD medication adherence.

Primary Outcome

Number of participants who completed the virtual education module at least once before the 30 day follow-up visit.

Conditions Studied

Interventions

  • OTHER BREATHES Program
  • DEVICE BREATHES SpiroPD or Propeller Health

Study Locations (1)

Illinois

  • University of Chicago Medicine - Chicago

Trial Details

FieldValue
Enrollment Target 71 participants
Start Date 2019-04-11
Est. Completion 2021-06-23
Phase NA
University of Chicago

796 total trials

What the finished NCT03834350 record still lists

NCT03834350 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, below the 2,418-participant average among 85 other COPD trials with a reported enrollment target (97% lower).

The record links to 1 condition, with COPD appearing as the primary indexed condition, and to 2 interventions - of which BREATHES Program is the first listed.

NCT03834350 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT03834350 about?

NCT03834350 is a clinical study titled "At Home Spirometry and Video Module Education for COPD Patients". The central hypothesis is that patients hospitalized for COPD who subsequently complete the at-home BREATHES Program with V-TTG skill training and SpiroPD adherence support will retain increased medication knowledge, skill, self-efficacy, and adherence that otherwise decays substantially by 30 days ...

What is the current status of trial NCT03834350?

This trial is currently completed. It is a NA study. The enrollment target is 71 participants. The study started on 2019-04-11. Estimated completion is 2021-06-23.

What conditions does trial NCT03834350 study?

This clinical trial studies the following conditions: COPD.

What interventions are being tested in trial NCT03834350?

The interventions under investigation include: BREATHES Program (OTHER), BREATHES SpiroPD or Propeller Health (DEVICE).

Who is sponsoring clinical trial NCT03834350?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03834350 being conducted?

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

Similar trials for COPD

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.

Where NCT03834350's enrollment target sits among peer trials

71 45th of 85 higher than 41 of 85 other COPD trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other COPD trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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

  • NCT05452889 · 71 participants · Early Phase 1

    PET Image in PAH Patients

  • NCT05766943 · 71 participants · NA

    Reduction of Myopotential Interference With Smart Pass in S-ICD Patients

  • NCT06229678 · 71 participants · Early Phase 1

    Ketones, SGLT2, HFrEF

  • NCT06377566 · 71 participants · Phase 2

    A Study of BV-AVD in People With Bulky Hodgkin Lymphoma

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 NCT03834350, the US trial registry maintained by the National Library of Medicine. NCT03834350 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.