Monitoring and Guidance of Physical Activity During the Maintenance Phase of Cardiac Rehabilitation: the Antwerp Activity Index

NCT ID: NCT07211282

Last Updated: 2025-10-07

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 318 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-10-15
• Study Completion Date: 2029-01-31

Brief Summary

The goal of this clinical trial is to determine whether the AAI activity score can help cardiac rehabilitation patients adhere to physical activity guidelines after participating in an in-hospital cardiac rehabilitation program. The main questions it aims to answer are:

1. Does the AAI activity score have an impact on adherence to physical activity maintenance during phase 3 CR?

2. Does the AAI activity score predict changes in cardiorespiratory fitness? Researchers will compare participants who use the AAI activity score with those who do not to determine if there are differences in physical activity adherence.

Participants will:

• Wear a smartwatch to continuously measure heart rate for 4 months;
• Perform an exercise stress test at the end of the study;
• Fill in several questionnaires at the end of the study.

Detailed Description

Adopting and maintaining an active lifestyle after phase 2 cardiac rehabilitation (CR) is crucial for cardiac patients. Tools to provide an active transition from phase 2 CR to phase 3 CR are lacking, resulting in negative changes in physical activity (PA) behaviour, cardiovascular risk profiles and cardiorespiratory fitness (CRF) levels. The researchers developed a procedure that calculates a PA-score (Antwerp Activity Index; AAI) based on reliable heart rate (HR) data collected by commercially available heart rate monitors (HRMs), which is designed to reflect changes in CRF. This procedure could serve as a valuable tool to facilitate a more active transition from phase 2 CR to phase 3 CR. Ultimately, positively influencing CR patients' PA levels (and possibly) cardiovascular and overall health-related outcomes.

This study will collect HR data with the Fitbit Versa 4 smartwatch and Polar H10 chest strap with the aim of:

Goal 1. Assessing the effect of our AAI-score intervention on adherence towards physical activity maintenance of post-phase 2 CR patients during phase 3 CR.

Goal 2. Assessing the potential differences in the participants' self-experienced physical activity and objectively measured physical activity.

Goal 3. Investigating the correlation between adherence to our AAI score and changes in CRF.

Goal 4. Measuring the adherence to our AAI score intervention. Goal 5. For a subpopulation of AF patients, we will analyse whether the AAI score intervention influences AF recurrence and burden.

Goal 6. Analysing technical outcomes regarding the use of the AAI score and the accompanying application. This will include system performance as well as user interaction with different elements of the application.

Patients complying with the inclusion criteria who completed phase 2 CR of two large care facilities and who are interested will be randomised into one of two groups:

Group 1: Patients who, after following the standard multidisciplinary in-hospital phase 2 CR trajectory, receive a Fitbit Versa 4 and our application with our AAI-score and who receive regular feedback (intervention group).

Group 2: Patients who, after following the standard multidisciplinary in-hospital phase 2 CR trajectory, receive a Fitbit Versa 4 with blinded AAI data collection and no feedback (control group - standard care).

Participants start with a run-in period wherein their eligibility for continuous PPG-HR tracking will be objectively measured. Objective eligibility will be determined by correlation of the Fitbit HR with the Polar HR (Polar H10 chest strap). The eligibility assessment will take place in the three consecutive CR training sessions scheduled for the participant. If deemed ineligible, the participant's participation in the study ends. Participants deemed eligible during the run-in period will be randomised to the intervention or control group.

All included participants will use the Fitbit device for an average of four months. Patients are instructed to continuously wear the Fitbit Versa 4 smartwatch for the whole monitoring period, sync the data daily via the Fitbit application, and charge the device when needed. The intervention group has access to the generated AAI scores through a study application. During an initiation visit, participants will be informed about how the score works and its purpose. The intervention group will receive tailored targets to adhere to. This group will also receive semi-automatic feedback reports through the application. Feedback will be provided every two weeks for the first two months and once more at the end of the third month. No feedback will be given during the last month of follow-up. Feedback is solely based on the collected scores and not on the values used to calculate the score (heart rate). Feedback is limited to overviews of recent days and motivational messages aimed at maintaining or increasing their scores. The control group also receives the Fitbit device but does not have access to the scores generated by the AAI algorithm or receive feedback through the Cardio2U application. This simulates current standard care. The AF subpopulation of both groups will also receive a license to use the FibriCheck application for the duration of the study. An application of the same name will accompany this. These measurements are taken in the background without participant intervention. At the end of the 4-month follow-up period, both the intervention and control groups will perform an exercise stress test. At this moment, the study ends, and all related devices are returned to a study team member. During this visit, a study team member will assist participants in completing two IPAQ questionnaires, which will assess their PA levels over the last two weeks. Through a personal online link, participants will also be asked to complete a quality of life questionnaire (SF-36), a self-developed experience questionnaire (PREM) and a digital health readiness questionnaire (DHRQ). The use of the AAI score through the application will be monitored throughout the entire study period, which occurs automatically without participant intervention.

Conditions

Cardiac Rehabilitation; Cardiovascular Disease Prevention

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

AAI usage through personalised target

Participants are instructed to continuously wear a Fitbit Versa 4 smartwatch for the whole monitoring period, sync the data daily via the Fitbit application, and charge the device when needed. The intervention group has access to the generated AAI scores through a study application. During an initiation visit, they will be informed about how the score works and its purpose. They will receive tailored targets to adhere to. This group will also receive semi-automatic feedback reports through the study application. Feedback will be provided every two weeks for the first two months and once more at the end of the third month. No feedback will be given during the last month of follow-up.

Group Type: EXPERIMENTAL

Activity score

Intervention Type: DEVICE

4 month follow-up and feedback from a heart rate and personal characteristics based activity score.

Blinded AAI data collection

Participants are instructed to continuously wear a Fitbit Versa 4 smartwatch for the whole monitoring period, sync the data daily via the Fitbit application, and charge the device when needed. They can use the device to their liking. They do not have access to the AAI algorithm, nor will they receive feedback through the study application.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Activity score

4 month follow-up and feedback from a heart rate and personal characteristics based activity score.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Age ≥ 18 years,

2. Patients in the last phase of phase 2 CR,

3. Having a smartphone available,

4. Being capable of signing the informed consent.

Exclusion Criteria

1. Patients with high-risk criteria for safe exercise participation following a cardiac event, including:

1. Ejection fraction less than 30%

2. Decrease in systolic blood pressure of more than 15 mmHg with exercise

3. Serious arrhythmias at rest or exercise-induced

4. Exercise-induced ischemia indicated by angina more than 2 mm ST segment depression on the ECG

2. Patients with severe heart failure (NYHA III-IV),

3. Patients with implantable devices (e.g. pacemakers),

4. Patients diagnosed with permanent AF,

5. Patients who do not speak and read Dutch or English,

6. Patients who have cognitive impairment (e.g. severe dementia).

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Universiteit Antwerpen

OTHER

Sponsor Role: collaborator

Jessa Hospital

OTHER

Sponsor Role: collaborator

University Hospital, Antwerp

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Hein Heidbuchel

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Antwerp

Locations

University Hospital Antwerp

Edegem, Antwerp, Belgium

Jessa Hospital Hasselt

Hasselt, Limburg, Belgium

Countries

Belgium

Central Contacts

Christophe Buyck

Role: CONTACT

christophe.buyck@uantwerpen.be

+32 3 821 42 03

Lien Desteghe

Role: CONTACT

lien.desteghe@uantwerpen.be

+32 821 33 06

Facility Contacts

Christophe Buyck

Role: primary

christophe.buyck@uantwerpen.be

+32 821 42 03

Anouk Delaet

Role: primary

anouk.delaet@uhasselt.be

+32 11 33 70 88

Other Identifiers

G084023N

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

BUN3002025000061

Identifier Type: -

Identifier Source: org_study_id