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FeelFit: high-intensity interval training to improve self-reported physical fitness in brain tumor patients: a randomized controlled trial

FeelFit: high-intensity interval training to improve self-reported physical fitness in brain tumor patients: a randomized controlled trial - FeelFit

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON56527
Enrollment
36
Registered
2023-10-12
Start date
2024-03-22
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

brain tumor primary brain tumor

Interventions

The intervention consists of performing a training program called high-intensity interval training which lasts for 12 weeks with two training sessions per week. The training sessions will be perform

Sponsors

Amsterdam UMC
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - minimum age of 18 years; - reduced self-reported physical fitness, defined as a score of "average", "poor" or "very poor" on the first question of the International Fitness Scale (IFIS): "My general physical fitness is?"; - diagnosed with a primary brain tumor; - stable disease, i.e. no signs of radiological or clinical tumor progression; - no oncological treatment for at least two months prior to inclusion; - able to speak, read and write in Dutch.

Exclusion criteria

Exclusion criteria: - Karnofsky Performance Score

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is self-reported physical fitness, measured by the first question of the International Fitness Scale (IFIS), "Your general physical fitness is?" On a scale of 1 ("very poor") to 5 ("very good").

Secondary

MeasureTime frame
The secondary outcome measure is maximum oxygen uptake (objective physical fitness; VO2max), measured with a cardiopulmonary exercise test (CPET). In addition, a set of exploratory outcomes will be measured to examine the effects of the intervention. The measurements include a muscle strength measurement, MRI (optional), MEG (optional), neuropsychological assessment and various questionnaires. And last, focus groups will be planned to learn from patients perspectives of participating in high-intensity interval training. Last, we ask patients in the intervention and waiting-list control group to keep an exercise diary in the first three weeks and last two weeks of the intervention period, and the last two weeks of the follow-up period.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)