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Posterior Fossa Brain Tumor GroupNCT07810673

Physical Performance and Quality of Life in Children With Brain Tumors

An observational study of Posterior Fossa Brain Tumor Group and Healthy Control Group, run by Sarah Mohammed El-Abasiri at 1 site in Egypt.

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Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
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Trial summary

This study is designed to assess physical performance and quality of life in children with posterior fossa brain tumors compared to healthy children. The trial evaluates parameters such as physical endurance, balance, muscle strength, gait characteristics, and quality of life measures to understand the functional… Read more about this study

Who is it for?
Ages 7 to 10 yearsHealthy volunteers can take part
How many people
60 participants
Where
1 siteEgypt
Study dates
1 Dec 2025to 25 Dec 2026
Phase
Observational

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 7 to 10 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Study population: Pediatric patients diagnosed with posterior fossa brain tumors recruited from treatment centers, alongside an age-matched group of healthy children serving as controls.

Who may be able to join

  • - Children aged 7 to 10 years.
  • Confirmed diagnosis of posterior fossa brain tumors.
  • Medically stable and able to perform physical evaluations.
  • Age-matched healthy children aged 7 to 10 years.
  • No history of neurological, musculoskeletal, or oncological disorders.

Who cannot join

  • Associated severe cognitive or visual impairments preventing test comprehension.
  • Other concurrent major medical or orthopedic conditions affecting physical performance.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Sarah Mohammed El-Abasiri contact

+20 10 91906219

d.ahmed.saber1987@gmail.com

Egypt1 site, 1 recruiting
  • Maadi Military Hospital

    Cairo

    Sara M Elabasiry Mohamed, MSc, +20 10 91906219, d.ahmed.saber1987@gmail.com

    Recruiting

Other trials in Egypt

About this study

Official title: ASSESSMENT OF PHYSICAL PERFORMANCE AND QUALITY OF LIFE IN CHILDREN WITH BRAIN TUMORS.

This study is designed to assess physical performance and quality of life in children with posterior fossa brain tumors compared to healthy children. The trial evaluates parameters such as physical endurance, balance, muscle strength, gait characteristics, and quality of life measures to understand the functional impact of the condition.

What participants receive

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

Study groups in NCT07810673
Study groupRoleWhat they receive
Posterior Fossa Brain Tumor GroupChildren aged 7 to 10 years diagnosed with posterior fossa brain tumors.
Healthy Control GroupAge-matched healthy children acting as a control group.

What is being measured

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

  1. 6-Minute Walk Test (6MWT)

    Measures walking distance in meters to evaluate physical endurance and functional capacity.

    Measured: At baseline during the initial assessment

Timeline

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

  1. First posted9 Sep 2026
  2. Study start1 Dec 2025
  3. Primary completion1 Dec 2026 (estimated)
  4. Study completion25 Dec 2026 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07810673
Sponsor's protocol ID
P.T.REC/012/006217
Status last verified
Sep 2026
First submitted
3 Sep 2026
Last updated
9 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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