Step by step: a coaching program aims to keep heart patients moving after rehab
NCT ID NCT07723274
First seen Jul 23, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This trial tests whether a 9-month program called STEP COACH can help people with coronary artery disease stay physically active after completing cardiac rehab. Participants use their own smartwatch or smartphone to track steps and receive coaching on increasing both step volume and intensity. The study compares changes in daily moderate-to-vigorous physical activity between those who receive the program and those who get usual care alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a 9-month behavioral coaching program called STEP COACH that uses step targets and smartwatch tracking to encourage physical activity
- What this could lead to
- If it works, this program could help heart patients maintain higher physical activity levels after cardiac rehab, potentially reducing their risk of future heart problems.
- What could go wrong
- This is a relatively small trial, and the effect may be modest. Participants need to stay motivated for 9 months, and results may not apply to all heart patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 334 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Hospital admission for CAD (ST-elevation myocardial infarction (STEMI), non-ST-elevation myocardial infarction (NSTEMI), unstable angina pectoris (UAP), or stable angina pectoris (AP)) and/or having undergone a percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG); * Referral to cardiac rehabilitation; * 18 years of age or older; * Able to understand and perform study related procedures. Exclusion Criteria: * Unable to give informed consent; * Wheelchair-bound / not physically able to stand or walk; * Language barrier; * CABG surgery expected within 8 weeks after inclusion; * New York Heart Association class III or IV heart failure; * Participation in another interventional study targeting physical activity; * Already adhering to physical activity guidelines (i.e. on average \>8,000 steps/day (smartphone) or \>10,000 steps/day (smartwatch or smartband) in the 6 months prior to inclusion).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Bernhoven
Uden, 5406PT, Netherlands
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Canisius Wilhelmina Ziekenhuis
Nijmegen, 6532SZ, Netherlands
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Radboud university medical center
Nijmegen, 6525GA, Netherlands
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Rijnstate
Arnhem, 6815AD, Netherlands
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- SMART-I: SiroMax™ Multi-Center coronary artery lesion treatment - safety and feasibility study of SiroMax SCB in ISR and DNSV
- Hospital-to-Home transitional cardiac rehabilitation as a transition from Centre-Based cardiac rehabilitation after cardiac surgery: a Single-Blind randomised controlled trial
- Opportunistic screening of coronary artery calcium on Non-Gated routine chest CT using artificial intelligence: retrospective external validation and clinical risk stratification
- AI heart scan software aims to spot dangerous blockages without invasive probes
- A shot of nicorandil before stenting might keep blood flowing
- Can personalized breathing settings protect lungs during heart surgery?