Gentle gyrokinesis shows promise for easing fatigue in young cancer survivors
NCT ID NCT07137091
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a gentle exercise program called Gyrokinesis could help reduce cancer-related fatigue in children and teens who had been treated for a brain tumor. 80 participants who had finished active treatment at least a year earlier took part. The study measured fatigue using a questionnaire and physical endurance with a six-minute walk test.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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80 people
The number who actually took part.
- Started
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Oct 2025
- Finished
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Feb 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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12 to 18 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosed and treated for a brain tumor during childhood or adolescence (0-≤18 years). * Treated for a PBT during the previous 10 years, starting from date of diagnosis. * Aged ≥6 years 0 months at the start of the trial. * Off therapy/active treatment for pediatric brain tumor (PBT) for 12 months at the start of the trial. * No known signs of clinical or radiological tumor progression at last follow-up. * Danish is the sole or primary language (enabling provision of validated assessment tools). * Patient and family have provided consent for inclusion in the trial. Exclusion Criteria: * History of recent poorly controlled seizures. * Motor tics or Tourette syndrome (including family history of tic disorder). * Known diagnosis of Attention Deficit/Hyperactivity Disorder or Autism Spectrum Disorder. * Known diagnosis of Full Scale Intelligence Quotient (FSIQ) of \<50. * Pregnancy. Participants known to be pregnant or breastfeeding at screening/registration will not enrolled
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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faculty of physical therapy ,Cairo University
Cairo, 3753450, Egypt
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Other studies related to the condition(s) this trial covers.
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