REmotely Monitored, Mobile Health Supported Multidomain Rehabilitation Program With High Intensity Interval Training for COVID-19
Purpose
Multicenter, prospective, randomized controlled trial providing mobile health supported physical rehabilitation to 120 patients who have been critically ill with COVID-19 and who complete at least one exercise session.
Conditions
- COVID-19
- Critical Illness
- ICU Acquired Weakness
- PICS
- Cardiorespiratory Fitness
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Primary diagnosis of COVID-19 requiring hospital admission - Discharged or expected to be discharged directly home from the hospital (not to a skilled nursing facility, inpatient rehabilitation center, or long-term acute care hospital) - Able to ambulate with or without a gait aid prior to hospital discharge - Age ≥ 18 years
Exclusion Criteria
- Hospital discharge > 60 days unless readmitted to hospital in first 30 days, then 60 day window restarts and new exclusion is last hospital discharge > 60 days - Not ambulating independently prior to COVID-19 illness (use of a gait aid permitted) - Functional impairment resulting in inability to exercise at baseline - Inability or unwillingness to comply with the study requirements or unable or unwilling to follow coaching via mobile-health iPhone interaction - Any absolute contraindications to exercise, including but not limited to: - Recent (< 5 days) acute primary cardiac event - Unstable Angina - Uncontrolled dysrhythmias causing symptoms or hemodynamic compromise - Uncontrolled hypertension over 255 mmHg Systolic or 155 diastolic blood pressure - Symptomatic aortic stenosis - Uncontrolled symptomatic heart failure - Acute myocarditis or pericarditis - Suspected or known dissecting aneurysm - Any adverse changes during GXT (i.e., persistent oxygen saturation drop below 88% while on prescribed oxygen therapy or significant hypotension such as mean arterial blood pressure < 60 mmHg on 2 consecutive readings within 1 minute) - High risk for non-adherence as determined by screening evaluation - Any condition, including cognitive impairment, that, in the judgment of the investigator, precludes participation because it could affect subject safety or ability of subject to complete the study - Pregnant
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
Experimental REmotely Monitored, Mobile health supported Multidomain Rehabilitation Program with HIIT |
Patients will receive our REmotely monitored, Mobile health supported Multidomain Rehabilitation Program with High Intensity Interval Training Program (REMM-HIIT) with iWatch/iPhone. |
|
No Intervention Exercise education without personalized sessions or feedback |
Patients will receive an exercise handout and iWatch/iPhone. Patients return home to exercise without personalized instruction and coaching. |
|
Recruiting Locations
Birmingham, Alabama 35233
Peter Morris, MD
More Details
- Status
- Recruiting
- Sponsor
- Duke University
Detailed Description
REmotely Monitored, Mhealth (REMM) supported High Intensity Interval Training (HIIT) to improve recovery after hospital discharge in patients with COVID-19 will evaluate the feasibility of clinical-, physiological- and patient-centered outcomes associated with a remotely monitored, mobile health-supported high intensity interval rehabilitation exercise training to improve the functional recovery of survivors who have experienced critical illness with COVID-19 and have been discharged home from the hospital.