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Pilot Evaluation of the JHI Platform

Pilot Evaluation of the Janssen Healthcare Innovation Integrated Cardiovascular Rehabilitation Management Platform (JHI PLATFORM).

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01648673
Enrollment
500
Registered
2012-07-24
Start date
2012-08-31
Completion date
2017-04-30
Last updated
2020-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

Keywords

Coronary Artery Disease, Cardiac Rehabilitation

Brief summary

The main purpose of this pilot study is to evaluate an impact of JHI CR Platform on patient referral, recruitment and retention rates and overall patient satisfaction in cardiovascular rehabilitation programs at the HFHS.

Interventions

None listed

Sponsors

Henry Ford Health System
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men and women age 18 years old (inclusive) and older * Recent hospitalization at HFHS Main Campus hospital with one of the following diagnosis * Stable angina with medical management * Myocardial infarction (MI)/Acute coronary syndrome * Percutaneous Coronary Intervention (PCI) * Coronary Artery Bypass Graft (CABG) surgery * Heart valve surgical repair or replacement * Patients must be attending outpatient CR program at the HFHS Detroit location. * Willingness to participate in the study and follow study requirements * Willingness to respond to several surveys at the baseline and periodically during the study

Exclusion criteria

* Active substance abuse per medical record * Unstable psychiatric condition * Inability to exercise * Unstable medical condition that would prevent safe and regular exercise training * Uncorrected Severe Aortic Stenosis or Severe Mitral Stenosis * Inpatient referring physician feels that exercise in contra-indicated due to safety reasons or is ill advised due to other patient specific factors * LVAD, Heart Transplant. Although these patients qualify for CR, HFHS is not recruiting them due to difficulty in coordinating with surgical patients and their providers. In addition, there may also be surgical issues (infection, wound dehiscence, bone healing etc) that may reasonably interfere with exercise.

Design outcomes

Primary

MeasureTime frame
Patient referral, recruitment and retention rates and overall patient satisfaction.Beginning, middle, and end of participation.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026