Actively Recruiting

All Genders
NCT05500859

Swiss Secondary Prevention and Rehabilitation Registry

Led by University Hospital, Basel, Switzerland · Updated on 2025-07-22

4000

Participants Needed

1

Research Sites

832 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The SwissPR study is to continuously monitor patient characteristics and short- and long-term benchmark quality measures and outcomes of patients participating in a 12-week ambulatory CR program.

CONDITIONS

Official Title

Swiss Secondary Prevention and Rehabilitation Registry

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participation in an ambulatory cardiac rehabilitation program (all age groups)
  • Written informed consent
Not Eligible

You will not qualify if you...

  • Inability to follow an ambulatory cardiac rehabilitation program for more than 3 weeks
  • Unwillingness to provide informed consent
  • Inability to understand the informed consent due to language comprehension difficulties
  • Lack of discernment or mental capacity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Basel, Division of Outpatient Cardiology

Basel, Switzerland, 4031

Actively Recruiting

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Research Team

O

Otmar Pfister, Prof. Dr. med.

CONTACT

S

Steffen Biniasch

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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