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Not yet recruiting NCT07103239

Feasibility and Acceptability of Three Component Intervention for the Heart Failure Care for Rural Dwelling Participants

No phase Interventional Heart Failure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Video Based Visits, Remote Self-Care Education, Remote Patient Monitoring.
Who it may be relevant to
Registry conditions: Heart Failure. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose of this research study is to determine if using remote blood pressure monitoring and video-based consultation is an effective way to help patients in rural communities better manage their heart failure.

Interventions

  • Behavioral Video Based Visits
    Video based visit with Heart Failure team
  • Behavioral Remote Self-Care Education
    Self Guided Training
  • Behavioral Remote Patient Monitoring
    Participant will use home devices to monitor blood pressure and weight; Participant will then send results to RN educator

Primary outcome measures

  • Feasibility [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • diagnosis of Heart Failure
  • English speaking
  • primary residence in counties of interest

Exclusion criteria

  • N/A

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Factorial
Masking
Open label
Primary purpose
Treatment

Study locations

United States · 1 center
  • University of Alabama at Birmingham — Birmingham

Identifiers

NCT: NCT07103239 · IRB-300015100 · 1K23HL179489-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗