Development of a clinical assessment tool as instrument to monitor physical fitness

Responsiveness of the FitMáx© questionnaire

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON24945

Enrollment

Registered

2020-04-28

Start date

2021-01-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Oncologic patients

Interventions

Beside the exercise intervention which is part of the usual care, no interventions are used in this trial.

Eligibility

Inclusion criteria

Inclusion criteria: - Patients who are participating in a rehabilitation programme or exercise intervention and who perform a cardiopulmonary exercise test before and after the intervention in Maastricht UMC+ - Signed informed consent is received

Exclusion criteria

Exclusion criteria: - Patients younger than 18 years - (subjective) Submaximal exercise test due to early abortion of the test - Incomplete questionnaire

Design outcomes

Primary

Measure	Time frame
The criterion responsiveness of the FitMáx© questionnaire to measure individual changes inaerobic capacity. In other words: the level of agreement between the estimated change in VO2-peak by the FitMáx© and the actual measured change in VO2-peak by the CPET.	—

Secondary

Measure	Time frame
- Is the FitMáx© questionnaire a more valid instrument to monitor physical fitness compared to existing/validated international questionnaires? - Is the FitMáx© questionnaire without the maximum cycling capacity, still a valid instrument to monitor physical fitness? (cultural adaptation for international use)	—

Contacts

Public ContactRenske Meijer

Máxima MC

renske.meijer@mmc.nl0637273149

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)