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Measuring physical activity during cardiac telerehabilitation using an accelerometer: a pilot study

Measuring physical activity during cardiac telerehabilitation using an accelerometer: a pilot study - Measuring physical activity during cardiac telerehabilitation using an accelerometer: a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON58331
Enrollment
25
Registered
2025-10-23
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Atherosclerotic cardiovascular disease Coronary artery disease

Interventions

Participants receive a Garmin Vivosmart 5 accelerometer to continuously monitor step count and physical activity. The device synchronizes with the Luscii app via Apple Health, enabling real-time feedb
standard CR continues unchanged.&nbsp

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Participation in the BRIDGE study Providing informed consent to participate in the GADGET study 18 + years old Coronary artery disease which is defined as: Myocardial infarction (STEMI or NSTEMI) Coronary revascularisation (CABG and/or PCI) Referred for and enrolled in outpatient CR Choosing to participate in cardiac telerehabilitation using the Luscii app as part of the standard BC program In possession of an iPhone (for compatibility with intervention tools) Sufficient digital literacy to operate the mobile health application independently or with minimal assistance 

Exclusion criteria

Exclusion criteria: Contraindication to CR Participating in centre based CR Stable angina pectoris Communication problems (such as language barrier) Participating in CR elsewhere (not at the study site) Unable or unwilling to provide written informed consent Severe cognitive impairment, psychiatric illness, or neurological condition that interferes with participation Lack of digital skills, even with available assistance Non access to an iPhone Participation in another interventional study that could interfere with the outcomes 

Design outcomes

Primary

MeasureTime frame
Physical activity measured with the International Physical Activity Questionnaire – Short Form (IPAQ-SF) at baseline, 3, 6, and 12 months. 

Secondary

MeasureTime frame
Quality of life (SF-36), Anxiety and depression (HADS), User experience and satisfaction (EHIQ) and Functional capacity Modified (Incremental Shuttle Walk Test) 

Countries

Netherlands

Contacts

Public ContactRFR Mierlo

Zuyderland

rutger.vanmierlo@maastrichtuniversity.nl0630135339

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Feb 7, 2026