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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05449652
Other study ID # AXXON
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 16, 2022
Est. completion date April 30, 2022

Study information

Verified date July 2022
Source Hasselt University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Physiotherapists are often confronted with patients with (elevated risk for) cardiovascular disease (CVD), even when this is not the primary indication for physiotherapy. Hence, physiotherapists should be able to provide evidence-based exercise advice to these patients, but this has not been assessed. The aim of this study was therefore to assess whether exercise prescriptions by physiotherapists to patients with CVD are in accordance with international recommendations.


Description:

In this prospective observational survey, forty-seven Belgian physiotherapists agreed to prescribe exercise intensity, frequency, session duration, program duration, and exercise type (endurance or strength training) for the same three patient cases. Exercise prescriptions were compared between clinicians and relations with clinician characteristics were studied. In addition, the agreement between physiotherapists' exercise prescriptions and those from international recommendations (based on a maximal score of 60/per case) was assessed.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date April 30, 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: Currently professionally active Flemish physiotherapists Exclusion Criteria: Not having access to a device that allows the use of the EXercise Prescription in Everyday practice & Rehabilitative Training (EXPERT) tool.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
To prescribe exercise prescription for CVD patients
To prescribe exercise intensity, frequency, session duration, program duration, and exercise type (endurance or strength training) for the same three patient cases

Locations

Country Name City State
Belgium Hasselt University Diepenbeek Limburg

Sponsors (1)

Lead Sponsor Collaborator
Hasselt University

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Exercise intensity Assessment of the prescription of exercise intensity (expressed in heart rate in beats per minute) February - April 2022
Primary Exercise frequency Assessment of exercise frequency (expressed in number of exercise sessions per week) February - April 2022
Primary Session duration Assessment of session duration (expressed in number of minutes) February - April 2022
Primary Program duration Assessment of program duration (expressed in number of weeks) February - April 2022
Primary Exercise type Aerobic exercise or strength exercise February - April 2022
Primary Total exercise volume Multiplication of number of prescribed weeks, number of prescribed sessions/week, prescribed individual session duration and prescribed exercise intensity February - April 2022
Secondary Association between exercise prescriptions and clinician characteristics' Relations between exercise prescriptions (intensity, frequency, session/program duration, exercise type) and clinician characteristics (age, gender, education, experience,...) were studied. February - April 2022
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