Mobile Health Technology-Enabled AFib Management
Eligible age
18+ yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
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About this study
The overall objective of this proposal is to evaluate the effect on quality of life of a comprehensive digital atrial fibrillation (AFib) management tool that will empower patients to a) take an active role in learning about AFib management options, starting and adhering to evidence-based therapies and lifestyle changes and b) to guide the patients during AFib episodes which are associated with anxiety and impairment in quality of life. Researchers plan to evaluate the effectiveness of this novel digital toolkit in improving quality of life and decreasing AFib burden in a randomized clinical trial (RCT). A pilot study assessing feasibility and retention of the intervention was previously conducted (NCT05400837)
Sponsor: Johns Hopkins University
You may qualify if…
- ✓ 1. Aged 18 or older at time of consent
- ✓ 2. Diagnosis of paroxysmal (Afib lasting less than 7 days) or persistent (7 days or longer) atrial fibrillation
- ✓ 3. BMI (Body Mass Index) ≥ 27.0
You may not qualify if…
- ✕ 1. Permanent Afib (decision has been made not to attempt sinus rhythm)
- ✕ 2. Severe valvular disease
- ✕ 3. Moderate mitral valve stenosis
- ✕ 4. Prior cardiac surgery
- ✕ 5. Presence of implanted cardiac device
- ✕ 6. History of cardiac arrest
- ✕ 7. Left ventricular ejection fraction (LVEF) ≤ 35%
- ✕ 8. Life expectancy \< 1 year
Where it's recruiting
Baltimore
Source: ClinicalTrials.gov · NCT06500988 · last updated 2026-04-20