Evaluate Heart Failure Patients With Specially Designed Patient Adherence and Monitoring Software on Standard Mobile Devices
Completed
Conditions studied: Cardiac Decompensation
In brief
This is planned as a feasibility study. The objective is to evaluate a specially designed patient adherence and monitoring software on standard mobile devices in remote monitoring of heart failure patients.
Key facts
- Study ID
- NCT01430936
- Run by
- Aventyn, Inc.
- People needed
- 51
- Starts
- 2011-01-01
- Expected to finish
- 2012-04-01
- Last updated by the study team
- 2012-07-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects of either gender above the age of 18 years
- The subject is able and willing to provide written informed consent prior to enrollment in the study
- New York Heart Association (NYHA) classification class of II-IV
- Left ventricular ejection fraction (LVEF) less than 40%
- One or more prior hospitalization within the last six months for symptoms, management of heart failure.
You may not qualify if…
- Disability of fingers or upper limbs (unable to use devices)
- Visually impaired
- Those unable to read and write
- Hearing dysfunction
- Significant cognitive disabilities, mental illness
- Those who are unable to handle electronic devices
- Those residing in places outside the local mobile phone coverage
- Chronic renal failure on renal replacement therapy
- Patients who may not come for follow up or likely to drop out of the study
- Those awaiting cardiac transplantation
- Any illness which may preclude regular follow up
Where it is running
- Winthrop University Hospital — Mineola, New York, United States
- Saint Francis Hospital — Roslyn, New York, United States
- Narayana Hrudayalaya Hospital — Bangalore, Karnataka, India
- Vivus-BMJ Heart Centre — Bangalore, Karnataka, India
- Karolinska University Hospital — Stockholm, Stockholm County, Sweden
Full record on ClinicalTrials.gov
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