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

NCT07211282 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 318

Last updated 2026-05-06

No results posted yet for this study

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.

Conditions

  • Cardiac Rehabilitation
  • Cardiovascular Disease Prevention

Interventions

DEVICE

Activity score

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

Sponsors & Collaborators

  • Universiteit Antwerpen

    collaborator OTHER
  • Jessa Hospital

    collaborator OTHER
  • University Hospital, Antwerp

    lead OTHER

Principal Investigators

  • Hein Heidbuchel · University Hospital, Antwerp

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-17
Primary Completion
2028-12-31
Completion
2029-01-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07211282 on ClinicalTrials.gov