Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02527759 · ClinicalTrials.gov registry record

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

A clinical trial, sponsored by Georgetown University.

Completed
Registry status
56
Enrollment target

NCT02527759: Completed study, sponsored by Georgetown University.

NCT02527759 is a clinical trial that has completed, run by Georgetown University. The registered enrollment target is 56 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02527759 has completed, sponsored by Georgetown University.

COMPLETED
Registry status
56 participants
Enrollment target

Study 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.

Primary Outcome

Trial a novel 30-day post-discharge monitoring instrument after hospitalization for heart to evaluate patient status based on patient self-monitoring.

Interventions

  • BEHAVIORAL Survey

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2016-01
Est. Completion 2017-08-30
Georgetown University

227 total trials

What the finished NCT02527759 record still lists

NCT02527759 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 56 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Survey is the first listed.

NCT02527759 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02527759 about?

NCT02527759 is a clinical study titled "Patient Self Monitoring to Evaluate 30 Day Post Discharge Heart Failure Outcomes". 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, i...

What is the current status of trial NCT02527759?

This trial is currently completed. The enrollment target is 56 participants. The study started on 2016-01. Estimated completion is 2017-08-30.

What interventions are being tested in trial NCT02527759?

The interventions under investigation include: Survey (BEHAVIORAL).

Who is sponsoring clinical trial NCT02527759?

This trial is sponsored by Georgetown University, which has 227 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02287428 · 56 participants · Phase 1

    Personalized NeoAntigen Cancer Vaccine w RT Plus Pembrolizumab for Patients With Newly Diagnosed GBM

  • NCT02923011 · 56 participants · Phase 3

    Comparative Effectiveness of MRgFUS Versus CTgRFA for Osteoid Osteomas

  • NCT02935283 · 56 participants

    Neuroimaging and Neuropsychological Outcomes in Urea Cycle Disorders

  • NCT03375866 · 56 participants · NA

    Effects of Mixed Nut Consumption on Satiety and Weight Management

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02527759, the US trial registry maintained by the National Library of Medicine. NCT02527759 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.