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NCT06205225 · ClinicalTrials.gov registry record · NA

iCardia4HF: Multi-component mHealth Intervention for Patients With Heart Failure

A NA study of Heart Failure, sponsored by University of Illinois at Chicago.

Recruiting
Registry status
NA
Development phase
360
Enrollment target
2
Study locations

NCT06205225: Recruiting NA study of Heart Failure, sponsored by University of Illinois at Chicago.

NCT06205225 is a NA study of Heart Failure that is actively recruiting participants, run by University of Illinois at Chicago. The registered enrollment target is 360 participants, below the 2,048-participant average among 397 other Heart Failure trials with a reported enrollment target (82% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06205225, a NA study of Heart Failure, is actively recruiting participants, sponsored by University of Illinois at Chicago.

RECRUITING
Registry status
NA
Development phase
360 participants
Enrollment target
2
Study locations

Study Summary

The goal of this factorial randomized trial is to examine the independent and synergistic efficacies of two mobile health technology interventions in people with chronic heart failure. The first intervention involves the use of multiple consumer mHealth apps and sensor devices (MyApps) for heart failure self-care (maintenance, monitoring, and management). The second intervention is a program of tailored text messages (Text4HF) targeting modifiable behavioral factors associated with heart failure self-care non-adherence. The main questions this study aims to answer are: 1. Can the use of consumer mHealth apps and devices (MyApps) improve heart failure self-care and reduce days lost due to cardiovascular hospitalization or death for any cause? 2. Can a program of individually tailored text messages (Text4HF) improve heart failure self-care and reduce the days lost due to cardiovascular hospitalization or death for any cause? 3. Can MyApps and Text4HF combined lead to greater improvements in heart failure self-care and days lost due to cardiovascular hospitalization or death for any cause

Primary Outcome

Hospitalization is defined as hospital admission resulting in an overnight stay where the length of stay is at least 24 hours. Events leading to emergency department visit only with a length of stay under 24 hours will not be classified as hospitalization. For a hospitalization to be considered as unplanned the patient must present new symptoms and/or worsening of existing symptoms with the need for immediate admission in a hospital for intensified care. A hospitalization will be considered "car

Conditions Studied

Interventions

  • BEHAVIORAL Text4HF
  • BEHAVIORAL MyApps
  • BEHAVIORAL MyApps & Text4HF
  • BEHAVIORAL Enhanced Usual Care

Study Locations (2)

Illinois

  • Rush University Medical Center - Chicago
  • University of Illinois Hospital & Health Sciences System - Chicago

Trial Details

FieldValue
Enrollment Target 360 participants
Start Date 2024-10-04
Est. Completion 2028-09-30
Phase NA
University of Illinois at Chicago

430 total trials

What NCT06205225 shows while recruiting

NCT06205225 is an interventional study that assigns participants to a tested intervention. The registered 360 participants enrollment target is mid-sized for trials with a published cap, below the 2,048-participant average among 397 other Heart Failure trials with a reported enrollment target (82% lower).

The record links to 1 condition, with Heart Failure appearing as the primary indexed condition, and to 4 interventions - of which Text4HF is the first listed.

NCT06205225 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT06205225 about?

NCT06205225 is a clinical study titled "iCardia4HF: Multi-component mHealth Intervention for Patients With Heart Failure". The goal of this factorial randomized trial is to examine the independent and synergistic efficacies of two mobile health technology interventions in people with chronic heart failure. The first intervention involves the use of multiple consumer mHealth apps and sensor devices (MyApps) for heart fai...

What is the current status of trial NCT06205225?

This trial is currently recruiting. It is a NA study. The enrollment target is 360 participants. The study started on 2024-10-04. Estimated completion is 2028-09-30.

What conditions does trial NCT06205225 study?

This clinical trial studies the following conditions: Heart Failure.

What interventions are being tested in trial NCT06205225?

The interventions under investigation include: Text4HF (BEHAVIORAL), MyApps (BEHAVIORAL), MyApps & Text4HF (BEHAVIORAL), Enhanced Usual Care (BEHAVIORAL).

Who is sponsoring clinical trial NCT06205225?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06205225 being conducted?

This trial has 2 study locations across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Heart Failure

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 NCT06205225's enrollment target sits among peer trials

360 123rd of 397 higher than 273 of 397 other Heart Failure trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Heart Failure 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

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Source: ClinicalTrials.gov NCT06205225, the US trial registry maintained by the National Library of Medicine. NCT06205225 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.