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RECRUITING NA

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

NCT06205225 · View on ClinicalTrials.gov ↗

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

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

Sponsor

University of Illinois at Chicago

421 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06205225

The ClinicalTrials.gov registry entry for NCT06205225 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 360 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Illinois at Chicago, which has 421 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06205225 reports 2 study locations spanning 1 distinct geographic area — top geographies include Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06205225?

The interventions under investigation include: Text4HF (BEHAVIORAL), MyApps (BEHAVIORAL), MyApps & Text4HF (BEHAVIORAL), Enhanced Usual Care (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06205225?

This trial is sponsored by University of Illinois at Chicago, which has 421 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial