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FatigueNCT07137091

Motion for Recovery: The Impact of Gyrokinesis on Childhood Cancer-Related Fatigue.

A study testing Gyrokinesis exercise in people with Fatigue, run by MTI University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

CRF influences engagement in everyday activities, mood, sleep, social relations, school attendance, academic achievement, and quality of life . It was significantly associated with low health-related quality of life in pediatric cancer patients including leukemia . Read more about this study

Who is it for?
Ages 12 to 18 years
Conditions the study is for
Fatigue
What is being tested?
Gyrokinesis exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteEgypt
Study dates
1 Oct 2025to 5 Feb 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • 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.

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • faculty of physical therapy ,Cairo University

    Cairo, 3753450

Other trials in Egypt

About this study

CRF influences engagement in everyday activities, mood, sleep, social relations, school attendance, academic achievement, and quality of life . It was significantly associated with low health-related quality of life in pediatric cancer patients including leukemia . Since attention to managing cRF has been drawn, only a few non-pharmacological strategies were tested for their effectiveness in reducing cRF among children. Physical activity (Pa) has been proven to be the most effective strategy . Yet adherence to Pa remains problematic.

Read the detailed description

Childhood cancer-related fatigue (CCRF) is a prevalent condition that affects the quality of life in pediatric cancer patients. Gyrokinesis, a holistic exercise method that incorporates principles from yoga, tai chi, and dance, offers potential benefits in managing fatigue through gentle movement and breath work.

According to The American Cancer Society (ACS) provides comprehensive guidelines for cancer training load .The intensity of the exercise refers to the amount of energy expended when performing the activity4. It can be measured subjectively with a self-reported estimate of effort called the rate of perceived exertion on a scale of 1-10. Low-intensity exercise refers to physical activity or effort performed at 1-3 times the intensity of baseline resting energy expenditure (<3 mets-for example, walking). Moderate-intensity exercise refers to physical activity 3-6 times the intensity of baseline, which requires a moderate amount of effort and noticeably accelerates the heart rate (3-6 mets-for example, brisk walking or cycling). Vigorous-intensity exercise refers to physical activity 6 or more times baseline, which requires a large amount of effort and causes rapid breathing and a substantial increase in heart rate (>6 mets-for example, running or jumping rope)

Conditions
Fatigue
Being tested
Gyrokinesis exercise
Medical subject headings
Fatigue

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Gyrokinesis exerciseOther

    1. Warm-Up:
    • Begin with gentle seated movements to prepare the body.
    • Focus on awakening the spine with small circles and undulating motions, coordinating with deep breathing.
    1. Seated Exercises:
    • Perform a series of exercises on a stool or chair.
    • Emphasize spinal articulation, pelvic tilts, and side bends while maintaining rhythmic breathing.
    1. Floor Work:
    • Transition to mat-based exercises focusing on core strength and flexibility.
    • Incorporate movements like leg lifts, spirals, and arching motions to engage different muscle groups.
    1. Standing Series:
    • Conclude with standing exercises to enhance balance and full-body integration.
    • Use spiral movements and weight shifts to energize the body and improve posture.
Study groups in NCT07137091
Study groupRoleWhat they receive
Gyrokinesis exerciseExperimentalStructure of a Gyrokinesis Session 1. Warm-Up: * Begin with gentle seated movements to prepare the body. * Focus on awakening the spine with small circles and undulating motions, coordinating with deep breathing. 2. Seated Exercises: * Perform a series of exercises on a stool or chair. * Emphasize spinal articulation, pelvic tilts, and side bends while maintaining rhythmic breathing. 3. Floor Work: * Transition to mat-based exercises focusing on core strength and flexibility. * Incorporate movements like leg lifts, spirals, and arching motions to engage different muscle groups. 4. Standing Series: * Conclude with standing exercises to enhance balance and full-body integration. * Use spiral movements and weight shifts to energize the body and improve posture.
Receives: Other: Gyrokinesis exercise
control groupNo interventionNo intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pediatric quality of life multidimensional fatigue scale (peds QLMFS):

    CRF was measured using the valid and reliable Arabic version of peds QlMFs . It is an 18-item questionnaire including 'general fatigue', 'sleep/rest fatigue', and 'cognitive fatigue'. The three child self-report versions were used depending on the child's age: 5-7 years (young child), 8-12 years (child), and 13-18 years (adolescent). Higher scores indicate less intense fatigue symptoms . Before the cOViD-19 pandemic, a paper-based appropriate version of the scale was completed by children. During the pandemic, the questionnaires were offered to the participants through a link sent to the parent's phones to eliminate cross-infection.

    Measured: at baseline and at 8 weeks

Secondary outcomes (3)
  1. The six-minute walk test (6-MWT)

    The 6-MWt is a functional test that measures the functional capacity/endurance and submaximal or maximal effort needed to perform activities of daily living . The primary outcome of this test is the distance covered in meters. a lower score reflects less functional capacity conceptualizing the child's inability to actively participate in functional activities due to cRF .the test is valid and reliable for children with cancer. Two small cones were placed to mark the starting and end points for a 25-meter-long corridor. The heart rate (hR) and oxygen saturation (spO2) were measured 10 min before and one minute after the 6-MWt according to the guidelines of the American thoracic society (ats).

    Measured: at baseline and at 8 weeks

  2. Emotional Well-Being

    The Children's Depression Inventory (CDI) is scored by summing the responses to its 27 items, with each item having three options scored 0, 1, or 2, resulting in a total score ranging from 0 to 54. Higher scores indicate more severe depressive symptoms.

    Measured: at baseline and at 8 weeks

  3. Blood panel test

    Blood samples were collected before and after the experiment to assess changes in serotonin and cortisol levels, as described previously . Venous blood samples (6 mL) were obtained from the antecubital vein using a disposable syringe between 8:00 a.m. and 10:00 a.m. after a fasting period of at least 8 hr. Capillary blood samples were also obtained via the fingertip method, with a minimum volume of 0.3 μL collected for analysis using a portable lactate analyzer. Cortisol can also be measured in the blood, with samples typically taken in the morning when levels peak

    Measured: at baseline and at 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Aug 2025
  2. Study start1 Oct 2025
  3. Primary completion1 Feb 2026
  4. Study completion5 Feb 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
RCT
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
80 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07137091
Sponsor's protocol ID
P.T.REC/012/005915
Status last verified
Feb 2026
First submitted
16 Aug 2025
Last updated
3 Mar 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Gyrokinesis exercise in people with Fatigue, run by MTI University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pediatric quality of life multidimensional fatigue scale (peds QLMFS): (time frame: at baseline and at 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Mar 2026.

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Clinical Trial NCT07137091 | AzTrials