Status:

COMPLETED

Supporting Post Myocardial Infarction (MI) Risk Modification Intervention Via Telemedicine Evaluation

Lead Sponsor:

Duke University

Collaborating Sponsors:

American Heart Association

Conditions:

Cardiovascular Disease

Eligibility:

All Genders

Phase:

NA

Brief Summary

The study is a three-arm design where up to 600 patients hospitalized post-MI are recruited from a large hospital and randomized to either the education group (control group) or one of the two interve...

Detailed Description

PURPOSE OF STUDY Cardiovascular disease (CVD) is the leading cause of death in the U.S., accounting for over one third of deaths. Of these, coronary heart disease (CHD) accounts for the greatest propo...

Eligibility Criteria

Inclusion

  • Admitted to Duke University Medical Center (DUMC) with both the diagnosis of acute MI (ICD code 410.01-410.91) and hypertension (ICD-9 code 401.X or clinical diagnosis)
  • A cardiac catheterization at DUMC within the past 3 years
  • Age \> 18 years
  • Established or planned follow-up with a primary care/cardiology provider within the Duke University Health System or its Affiliated Clinics

Exclusion

  • Medical Records Exclusion (occurs prior to mailing invitation):
  • Diagnosis of metastatic cancer in the past 6 months
  • Active diagnosis of psychosis or dementia
  • Currently receiving hemodialysis
  • Patients who have had a transplant
  • Patient-Level Exclusion (occurs at initial interview):
  • Does not have access to a telephone
  • Does not have access to a computer
  • Refusal to provide informed consent
  • Resident in nursing home or receiving home health care
  • Severely impaired hearing or speech (patients must be able to respond to phone calls)
  • Participating in another study (i.e., pharmaceutical trial)
  • NYHA class IV heart failure
  • Does not plan to have long-term follow-up with a primary care provider cardiologist

Key Trial Info

Start Date :

June 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2013

Estimated Enrollment :

416 Patients enrolled

Trial Details

Trial ID

NCT00901277

Start Date

June 1 2009

End Date

July 1 2013

Last Update

September 8 2014

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