Clinical Trials Directory

Trials / Completed

CompletedNCT02527759

Patient Self Monitoring to Evaluate 30 Day Post Discharge Heart Failure Outcomes

Status
Completed
Phase
Study type
Observational
Enrollment
56 (actual)
Sponsor
Georgetown University · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to examine the relative predictive ability of the derived monitoring instrument to determine post discharge instability and 30-day outcomes in patients discharged with HF. The primary hypothesis is that variables in the monitoring instrument, individually and combined, identify risk for 30-day outcomes. Clinical indicators of dyspnea, fatigue, orthopnea, dyspnea with exertion, daily weight, edema, heart rate, blood pressure, mental condition, medication adherence, and overall well-being will be reported by participants on a daily basis and considered indicators for 30-day outcomes of stability, re-hospitalization, or mortality.

Conditions

Interventions

TypeNameDescription
BEHAVIORALSurvey

Timeline

Start date
2016-01-01
Primary completion
2017-08-01
Completion
2017-08-30
First posted
2015-08-19
Last updated
2017-10-20

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02527759. Inclusion in this directory is not an endorsement.