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Clinical Trials/NCT03702062
NCT03702062WithdrawnNot Applicable

Dynamic Prediction of Heart Failure Using Real-time Functional Status and Electronic Health Record Data in the Ambulatory Setting

University of California, San Francisco1 site in 1 countryStarted: November 21, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Locations
1
Primary Endpoint
Heart failure hospitalization

Study Overview

Brief Summary

Heart failure is the number one cause of hospital readmission in those over 65 years of age and the current standard-of-care of weight self-monitoring is inadequate to predict exacerbation. This project aims to improve the monitoring of heart failure disease progression through the use of real-time, up-to-date data obtained both from a smart phone-based tool and from the electronic health record. The goal is to develop a low-risk, clinically validated method to estimate dynamic heart failure risk to enable the provision of earlier, more effective outpatient interventions that decrease hospitalization.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Hospitalized for decompensated heart failure
  • •Age >=18 years
  • •Owns a smart phone
  • •Willing to measure self assess 6 minute walk test weekly

Exclusion Criteria

  • Not provided

Arms & Interventions

Observational Arm

Experimental

Participants will be asked to measure self-assessed 6 minute walk test via the smart phone application twice a week for 2 months after discharge from a heart failure hospitalization, and weekly thereafter for 6 months.

Intervention: 6 Minute Walk Test Smart phone Application (Diagnostic Test)

Outcomes

Primary Outcomes

Heart failure hospitalization

Time Frame: 12 months

hospital inpatient admission or emergency room visit

Secondary Outcomes

  • Heart failure mortality(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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