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Clinical Trials/NCT06282562
NCT06282562
Recruiting
Not Applicable

FeelFit: High-intensity Interval Training to Improve Self-reported Physical Fitness in Brain Tumor Patients: a Randomized Controlled Trial

Amsterdam UMC, location VUmc1 site in 1 country36 target enrollmentJanuary 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Brain Tumor, Primary
Sponsor
Amsterdam UMC, location VUmc
Enrollment
36
Locations
1
Primary Endpoint
Self-reported physical fitness
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The FeelFit study aims to assess the effectiveness of High-Intensity Interval Training (HIIT) in improving self-reported physical fitness in adult brain tumor patients during periods of stable disease, as compared to a waiting-list control group. Furthermore, several secondary and exploratory outcomes will be evaluated. The study is part of the GRIP (GuaRding quality survivorshiP) project, which aims to improve quality of life in brain tumor patients.

Registry
clinicaltrials.gov
Start Date
January 1, 2024
End Date
August 15, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Amsterdam UMC, location VUmc
Responsible Party
Principal Investigator
Principal Investigator

Linda Douw

Principal Investigator

Amsterdam UMC, location VUmc

Eligibility Criteria

Inclusion Criteria

  • reduced self-reported physical fitness;
  • minimum age of 18 years;
  • 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

  • Karnofsky Performance Score \< 70;
  • already participated in a HIIT program \< 1 month prior;
  • contraindication of exercise.

Outcomes

Primary Outcomes

Self-reported physical fitness

Time Frame: Baseline versus post-intervention (12 weeks) and versus follow-up (12 weeks and 6 weeks follow-up)

Self-reported physical fitness is measured using the first question of the International Fitness Scale (IFIS) on general physical fitness, on a 5-point scale where a higher score corresponds to better self-reported physical fitness.

Secondary Outcomes

  • Self-reported fitness(Baseline versus post-intervention (12 weeks) and versus follow-up (12 weeks and 6 weeks follow-up))
  • VO2max(Baseline versus post-intervention (12 weeks))

Study Sites (1)

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