Smartphone Delivered In-home Cardiopulmonary Rehabilitation
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|ClinicalTrials.gov Identifier: NCT02791685|
Recruitment Status : Recruiting
First Posted : June 7, 2016
Last Update Posted : August 19, 2021
|Condition or disease||Intervention/treatment|
|Cardiovascular Disease Coronary Artery Disease||Behavioral: MULTIFIT Cardiac Rehabilitation Behavioral: Movn Pulmonary Rehabilitation Behavioral: Standard of Care Cardiac Rehabilitation|
This project aims to determine if a smartphone-delivered cardiac rehabilitation (CR) program could show similar clinical outcomes to in-person programs at a low cost in a large population of patients. Investigators will also assess the feasibility of tailoring a virtual CR program to a small sample of COPD participants who also stand to benefit in the absence of an established pulmonary rehabilitation (PR) program.
This is a non-randomized clinical trial of participants at the Atlanta Veterans Affairs Medical Center with an applicable diagnosis for cardiac or pulmonary rehabilitation versus usual care during the study period. We will evaluate the outcomes related to smartphone-enabled home base cardiopulmonary rehabilitation in those who choose the intervention and those who opt into home-based CR, traditional CR, or those who decline. Data from the past 5 years will also be evaluated to obtain a baseline event rate.
Investigators seek to address the following:
- Determine whether a home-based cardiac or pulmonary rehabilitation program delivered through smartphones is feasible and improves functional status.
- Determine if education and lifestyle counseling lead to increased adherence with prescribed follow-up, pharmacotherapy, quality of life, self-efficacy and lifestyle changes.
- Determine if a home-based cardiac or pulmonary rehabilitation program reduces health system utilization, including ED visits and readmission rates.
|Study Type :||Observational|
|Estimated Enrollment :||300 participants|
|Official Title:||Smartphone Delivered In-home Cardiopulmonary Rehabilitation|
|Study Start Date :||May 2016|
|Estimated Primary Completion Date :||September 2022|
|Estimated Study Completion Date :||December 2022|
Cardiac Rehabilitation - Movn Program
Participants with coronary artery disease (CAD) and chronic obstructive pulmonary disease (COPD) who are eligible for cardiac rehabilitation will undergo an in-home program.
Behavioral: MULTIFIT Cardiac Rehabilitation
MULTIFIT is a cardiac rehabilitation program delivered by the Movn smartphone application that will provide risk factor modification, prescribed exercises, education and counseling. The application will track activity using a built-in accelerometer or through connected devices such as a Fitbit for daily physical activity and management. Weight and blood pressure (BP) will be tracked by manual input or through wireless scales and BP monitors. The program will last for 12 weeks.
Pulmonary Rehabilitation - Movn Program
Participants with stable chronic obstructive pulmonary disease (COPD) or hospitalized with an acute exacerbation of COPD will undergo an in-home pulmonary rehabilitation program.
Behavioral: Movn Pulmonary Rehabilitation
Movn pulmonary rehabilitation is a program delivered by the Movn smartphone application that includes targeted educational content and prescribed exercises with mild resistance training in addition to walking and other cardiovascular exercises. The application will track activity using a built-in accelerometer or through connected devices such as a Fitbit for daily physical activity and management. Weight and blood pressure (BP) will be tracked by manual input or through wireless scales and BP monitors. The program will last for 12 weeks.
Traditional Cardiac Rehabilitation
Participants enrolled in a facility's traditional cardiac rehabilitation program will be seen at baseline and during a 12 and 24 week follow-up visit.
Behavioral: Standard of Care Cardiac Rehabilitation
Standard cardiac rehabilitation involves a facility's standard rehabilitation practices. Participants will be seen at baseline and during a 12 and 24 week follow-up visit.
- Change in Functional Capacity assessed by the Six Minute Walk Test (6MWT) [ Time Frame: Week 12, Week 24 ]The six-minute walk test (6MWT) measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface. The goal is for the individual to walk as far as possible in six minutes. The individual is allowed to self-pace and rest as needed as they traverse back and forth along a marked walkway.
- Change in Measure of Exercise Intensity (MET) [ Time Frame: Baseline, Week 12 ]An exercise test will be used to collect MET.
- Change in Weight [ Time Frame: Baseline, Week 12 ]Weight will be measured in kilograms.
- Change in Body Mass Index (BMI) [ Time Frame: Baseline, Week 12 ]Body Mass Index (BMI) is a person's weight in kilograms divided by the square of height in meters. A high BMI can be an indicator of high body fatness.
- Change in Blood Pressure [ Time Frame: Baseline, Week 12 ]
Blood pressure is measured using a blood pressure cuff to the upper extremity. The top number, which is also the higher of the two numbers, measures the pressure in the arteries when the heart beats (systolic).The bottom number, which is also the lower of the two numbers, measures the pressure in the arteries between heartbeats (diastolic). Readings are measured as follows:
Normal = systolic less than 120 and diastolic less than 80 Prehypertension = systolic 120 - 139 or diastolic 80 - 89 High Blood Pressure (Hypertension) Stage 1 = systolic 140 - 159 or diastolic 90 - 99 High Blood Pressure(Hypertension) Stage 2 = systolic 160 or higher or diastolic 100 or higher Hypertensive Crisis (Emergency care needed) systolic = higher than 180 or diastolic higher than 110
- Change in A1c Level [ Time Frame: Baseline, Week 12 ]
The A1C test is a blood test that provides information about a person's average levels of blood glucose, also called blood sugar, over the past 3 months.
Levels are measured as follows:
Normal = below 5.7 percent Diabetes = 6.5 percent or above Prediabetes = 5.7 to 6.4 percent
- Change in Low-density Lipoprotein (LDL) Level [ Time Frame: Baseline, Week 12 ]
LDL cholesterol is considered "bad" cholesterol because it contributes to plaque, a thick, hard deposit that can clog arteries and make them less flexible.
Levels are measured as follows:
< 100 mg/ dL = Optimal 100-129 mg/dL = Near optimal/above optimal 130-159 mg/dL = Borderline high 160-189 mg/dL = High >190 mg/dL = Very high
- Change in Duke Activity Status Index (DASI) Score [ Time Frame: Baseline, Week 12 ]The Duke Activity Status Index (DASI) is a 12-item questionnaire that utilizes self-reported physical work capacity to estimate peak metabolic equivalents. The DASI is scored by adding all activities performed together. A higher score indicates the ability to perform more physical activities.
- Change in Patient Health Questionnaire (PHQ-9) Score [ Time Frame: Baseline, Week 12 ]
The PHQ-9 is an instrument for screening, diagnosing, monitoring, and measuring the severity of depression.
Score ranges from 5-9 indicate minimal depressive symptoms. Scores 10-14 may indicate minor depression, dysthymia, and mild major depression. Scores 15-19 indicate moderately severe, major depression. Scores greater than or equal to 20 indicate severe major depression.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02791685
|Contact: Amit Shah, MDemail@example.com|
|United States, Georgia|
|Atlanta VA Medical Center||Recruiting|
|Atlanta, Georgia, United States, 30033|
|Contact: Amit Shah, MD 404-321-6111 ext 205523 firstname.lastname@example.org|
|Principal Investigator:||Amit J Shah, MD||Emory University|