NCT06345807Not yet recruiting
Innovative Care Pathway in Physical Activity and Behavior Change in Coronary Patients Post-cardiac Rehabilitation
Innovative Care Pathway in Physical Activity and Behavior Change in Coronary Patients Post Cardiac Rehabilitation
Source: ClinicalTrials.gov · Last updated 3 Sept 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The objective of this 18-month research is to show the effectiveness of an individualized physical activity( PA) compared to standard PA management and voluntary PA, to achieve a change in the behavior of the coronary patient.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 192 (estimated)
- First submitted
- 28 Mar 2024
- Start date
- 1 Oct 2024
- Primary completion date
- 30 Nov 2026
- Lead sponsor
- Elsan
- Diseases
- Coronary artery disease
- NCT number
- NCT06345807
What you commit to
- Study type: Interventional
- Planned participants: 192
- From 1 Oct 2024 to the primary completion date, 30 Nov 2026
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Patients with a formal contraindication to physical activity such as: unstabilized coronary syndrome, decompensated heart failure, severe ventricular arrhythmias, intracardiac thrombus at risk embolic, PAH, moderate pericardial effusion, history of thrombophlebitis with or without pulmonary embolism, severe and/or symptomatic left ventricular ejection obstruction.
- Patients with ongoing infectious disease
Other
- Participant whose physical and/or psychological health is severely impaired, which in the opinion of the investigator may affect the study participant's compliance.
- Participant included in other research
- Participant in a period of exclusion from another research still in progress at the time of inclusion.
- Protected participant: an adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision.
- Pregnant, breastfeeding or parturient women.
- Participant hospitalized without consent.
Who the study is looking for
- Post-infarction coronary artery patient aged 18 years and older, with no gender difference.
- Patients engaged in a follow-up care and cardiovascular rehabilitation program at the Supervaltech center.
- Patient at low to moderate RARE risk of complication (RARE score 2 to 3)
- Patients equipped with smartphones, laptops or other equipment compatible with downloading an application with their personal ID
- Patient able to understand French for the purpose of conducting the study.
- Affiliated member or beneficiary of a social security scheme.
- Participant who has been informed and has given free, informed and written consent (no later than the day of inclusion and before any examination required by the research).
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.