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Homebased Training With Telemonitoring Guidance in Low to Moderate Risk Patients Entering Cardiac Rehabilitation

Effects of Homebased Training With Telemonitoring Guidance in Low to Moderate Risk Patients Entering Cardiac Rehabilitation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01732419
Acronym
FIT@Home
Enrollment
90
Registered
2012-11-22
Start date
2013-01-31
Completion date
2015-10-31
Last updated
2019-08-29

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

Conditions

Acute Coronary Syndrome, Myocardial Infarction

Keywords

Rehabilitation, exercise therapy, coronary artery disease

Brief summary

Physical exercise training appears effective for low to moderate patients assigned to cardiac rehabilitation. However, adherence to cardiac rehabilitation is low and physical activity levels often drop after attending the last supervised rehabilitation session. This study will compare home based physical exercise training including telemonitoring with regular centre based physical exercise training. Main outcome measures are the change in physical activity and the change in physical fitness (peak Oxygen uptake) after the initial rehabilitation period (12 weeks) and after 1 year. Secondary outcome measures are cost-effectiveness, training adherence, health-related quality of life and patient satisfaction.

Detailed description

Physical training has beneficial effects on exercise capacity, cardiac function, quality of life and mortality in patients with acute cardiovascular syndrome or after cardiac surgery and is therefore one of the main aspects of cardiac rehabilitation. However, adherence to this therapy is low and effects tempt to decrease directly after the treatment period. The objective of this study is to compare the effects of home-based exercise training (HT) with telemonitoring guidance and regular centre-based exercise training (CT) on physical fitness (PF), assessed by peak oxygen uptake, and physical activity (PA), assessed by physical activity energy expenditure (PAEE), in low to moderate risk cardiac rehabilitation (CR) patients. Secondary endpoints are cost-effectiveness, training adherence, health-related quality of life (QoL) and patient satisfaction. Single-centre randomized controlled trial. CR patients are randomized to HT (n=45) or CT (n=45). Assessments are performed at baseline, 12 weeks and 1 year, consisting of maximal exercise testing with respiratory gas exchange analysis, assessment of PAEE, QoL (also at 6 months), patient satisfaction (at 12 weeks only) and health care costs (12 weeks, 6 months and 1 year) Study population: Low to moderate risk patients entering outpatient CR after an acute coronary syndrome or revascularization with internet access and PC at home. 12-week training program (24-36 one-hour sessions) at 70-85% of their maximal heart rate (HR). In the CT group training is supervised by a physical therapist; in the HT group training is performed in the home environment using a HR monitor to determine training intensity and with weekly feedback / motivation by an exercise specialist who has access to the online HR-data. After 12 weeks, subjects in the HT group are encouraged to continue using the HR monitor. Main study parameters/endpoints: Primary endpoints: PF (peak oxygen uptake) and PA (physical activity energy expenditure, PAEE) assessed by a tri-axial accelerometer and HR monitor. Secondary endpoints: training adherence, QoL (SF-36) and patient satisfaction (CQ index). Exercise training performed by patients after Acute Coronary Disease (ACS) and revascularization, classified as low to moderate risk, is considered to be safe. The training program that will be used in this study has been evaluated in a similar population of elderly cardiac patients without any documented harmful effects. In order to reduce potential risks of exercise training all patients perform a maximal cardiopulmonary exercise test at baseline, excluding patients with myocardial ischaemia and ventricular arrhythmias during exercise. The first three training sessions will be under supervision of trained physiotherapist in a clinical setting. The patients will receive a heart rate monitor and accelerometer to use at home. These monitors are developed and optimized to cause minimal physical discomfort and are non-invasive. During the measurement periods, all patients are asked to wear the monitors continuously for 5 days and to note the physical activities performed. The HT group will use the HR monitors during their physical trainings as well.

Interventions

Home-based exercise training for cardiac patients.

BEHAVIORALCentre-based training

Usual exercise training in an outpatient setting.

Sponsors

Maxima Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients with an ACS (including non ST and ST elevation myocardial infarction and unstable angina) or a cardiac revascularization procedure (PCI or CABG) entering outpatient CR at Maxima Medical Center. * Indication for exercise training according to the Dutch clinical algorithm for assessment of patient needs in cardiac rehabilitation. * Internet access and PC at home (i.e. more than 90 percent of the Dutch household)

Exclusion criteria

* High risk according to the Dutch CR practice guideline. * Systolic heart failure (left ventricular ejection fraction of more than 40 percent. * New York Heart Association class III-IV (i.e. breathlessness during light exercise or at rest). * Severe arrhythmia. * Hemodynamically significant valvular disease. * Implantable cardioverter-defibrillator (ICD) implantation * Heart transplantation. * Chronic angina or silent ischemia. * Comorbidity impairing exercise capacity (e.g. COPD, diabetes mellitus, peripheral vascular disease and orthopedic or neurological conditions). * Severe psychological or cognitive impairments.

Design outcomes

Primary

MeasureTime frameDescription
Physical FitnessMeasured after 12 weeks and after one yearChanges in peak oxygen uptake (VO2max) in mL O2/kg/min
Physical Activity Level (PAL)measured after 12 weeks and after one yearPAL is calculated by combining data from an accelerometer with data from a heart monitor, after wearing both for five days continuously. To determine PAL, physical activity energy expenditure is divided by resting metabolic rate, calculated by the Harris-Benedict equation. PAL expressed a person's daily energy expenditure. When PAL is used to classify the intensity of an activity, PAL\<3, PAL\<6 and PAL\>6 are characterized as light, moderate and vigorous intensity activities respectively. An average daily PAL of 1.2 represents the activity level of a bed-bound subject, while the average PAL for the adult population is 1.7.

Secondary

MeasureTime frameDescription
Training Adherence12 weeksProvides information on the average amount of training sessions were performed during the 12 week cardiac rehabilitation program. Both groups received the advice to train at least 2 times a week for 12 weeks (thus 24 sessions).
Health Related Quality of Lifemeasured at baseline, at discharge (12 weeks), and follow-up (one year)Health-related quality of life will be assessed by the MacNew questionnaire. The items and scale are scored from 1 (low health-related Quality of Life) to 7 (High health-related Quality of Life).
Patient SatisfactionMeasured at CR discharge (12 weeks)Patient satisfaction is measured directly after CR discharge (12 weeks) using the Consumer Quality Index, a standardized survey method combining the inventory of patient experiences with an assessment of their priority. Results are provided on a scale of 1 (very low satisfaction) to 10 (very high satisfaction).

Countries

Netherlands

Participant flow

Participants by arm

ArmCount
Home-based Training
After the first three supervised training sessions in the hospitals, patients in the home-based training group are instructed to wear a heart rate monitor during exercise training at home. Prescribed exercise exists of two or three exercise sessions per week, of one hour at 70 - 85% of their maximum heart rate. Once a week the heart rate data is uploaded and evaluated by an exercise specialist together with the patient by telephone. Home-based training: Home-based exercise training for cardiac patients.
45
Centre-based Training
Patients in the centre-based training group will perform all trainings sessions under direct supervision of a physical therapist specialized in CR. Training sessions will be performed on an cycle ergometer, starting with a warm up phase of 5 min, followed by 50 min of cycling at 70-85% of the maximal HR and a cooling down period of 5 min. During the training period, physical therapists will record attendance, training duration and actual training intensity. After the 12-week training period patients receive individual advice from their physical therapist on physical activities. Centre-based training: Usual exercise training in an outpatient setting.
45
Total90

Baseline characteristics

CharacteristicHome-based TrainingCentre-based TrainingTotal
Age, Continuous60.5 years
STANDARD_DEVIATION 8.8
57.7 years
STANDARD_DEVIATION 8.7
59.2 years
STANDARD_DEVIATION 8.5
Region of Enrollment
Netherlands
45 participants45 participants90 participants
Sex: Female, Male
Female
5 Participants5 Participants10 Participants
Sex: Female, Male
Male
40 Participants40 Participants80 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 450 / 45
serious
Total, serious adverse events
3 / 459 / 45

Outcome results

Primary

Physical Activity Level (PAL)

PAL is calculated by combining data from an accelerometer with data from a heart monitor, after wearing both for five days continuously. To determine PAL, physical activity energy expenditure is divided by resting metabolic rate, calculated by the Harris-Benedict equation. PAL expressed a person's daily energy expenditure. When PAL is used to classify the intensity of an activity, PAL\<3, PAL\<6 and PAL\>6 are characterized as light, moderate and vigorous intensity activities respectively. An average daily PAL of 1.2 represents the activity level of a bed-bound subject, while the average PAL for the adult population is 1.7.

Time frame: measured after 12 weeks and after one year

Population: Patients finished the study

ArmMeasureGroupValue (MEAN)Dispersion
Home-based TrainingPhysical Activity Level (PAL)Baseline2.09 PALStandard Deviation 0.92
Home-based TrainingPhysical Activity Level (PAL)Discharge CR (12 weeks)2.22 PALStandard Deviation 0.99
Home-based TrainingPhysical Activity Level (PAL)Follow up (1 year)2.14 PALStandard Deviation 1.06
Centre-based TrainingPhysical Activity Level (PAL)Baseline1.95 PALStandard Deviation 0.86
Centre-based TrainingPhysical Activity Level (PAL)Discharge CR (12 weeks)2.38 PALStandard Deviation 1.02
Centre-based TrainingPhysical Activity Level (PAL)Follow up (1 year)2.13 PALStandard Deviation 1
Primary

Physical Fitness

Changes in peak oxygen uptake (VO2max) in mL O2/kg/min

Time frame: Measured after 12 weeks and after one year

Population: patients finished the study

ArmMeasureGroupValue (MEAN)Dispersion
Home-based TrainingPhysical FitnessBaseline24.4 ml O2/kg/minStandard Deviation 6.7
Home-based TrainingPhysical FitnessDischarge CR (12 weeks)27.9 ml O2/kg/minStandard Deviation 7.5
Home-based TrainingPhysical FitnessFollow up (1 year)27.7 ml O2/kg/minStandard Deviation 6.9
Centre-based TrainingPhysical FitnessBaseline24.0 ml O2/kg/minStandard Deviation 5.6
Centre-based TrainingPhysical FitnessDischarge CR (12 weeks)26.5 ml O2/kg/minStandard Deviation 7.1
Centre-based TrainingPhysical FitnessFollow up (1 year)27.5 ml O2/kg/minStandard Deviation 8.1
Secondary

Health Related Quality of Life

Health-related quality of life will be assessed by the MacNew questionnaire. The items and scale are scored from 1 (low health-related Quality of Life) to 7 (High health-related Quality of Life).

Time frame: measured at baseline, at discharge (12 weeks), and follow-up (one year)

Population: Patients finished the study

ArmMeasureGroupValue (MEAN)Dispersion
Home-based TrainingHealth Related Quality of LifeBaseline5.62 Units of a scaleStandard Deviation 0.2
Home-based TrainingHealth Related Quality of LifeDischarge CR (12 weeks)6.00 Units of a scaleStandard Deviation 0.13
Home-based TrainingHealth Related Quality of LifeFollow up (one year)5.75 Units of a scaleStandard Deviation 0.1
Centre-based TrainingHealth Related Quality of LifeBaseline5.45 Units of a scaleStandard Deviation 0.14
Centre-based TrainingHealth Related Quality of LifeDischarge CR (12 weeks)5.90 Units of a scaleStandard Deviation 0.13
Centre-based TrainingHealth Related Quality of LifeFollow up (one year)5.43 Units of a scaleStandard Deviation 0.12
Secondary

Patient Satisfaction

Patient satisfaction is measured directly after CR discharge (12 weeks) using the Consumer Quality Index, a standardized survey method combining the inventory of patient experiences with an assessment of their priority. Results are provided on a scale of 1 (very low satisfaction) to 10 (very high satisfaction).

Time frame: Measured at CR discharge (12 weeks)

Population: Patients finished the CR program (12 weeks)

ArmMeasureValue (MEAN)Dispersion
Home-based TrainingPatient Satisfaction8.7 units on a scaleStandard Deviation 1
Centre-based TrainingPatient Satisfaction8.1 units on a scaleStandard Deviation 1.2
Secondary

Training Adherence

Provides information on the average amount of training sessions were performed during the 12 week cardiac rehabilitation program. Both groups received the advice to train at least 2 times a week for 12 weeks (thus 24 sessions).

Time frame: 12 weeks

Population: Patients finished the CR program

ArmMeasureValue (MEAN)Dispersion
Home-based TrainingTraining Adherence22.0 Exercise sessions completedStandard Deviation 6.8
Centre-based TrainingTraining Adherence20.6 Exercise sessions completedStandard Deviation 4.3

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026