Structured Wii Aerobic Protocol on Reaction Time and Pulmonary Functions in Over Weight School- A… (NCT07513298) | Clinical Trial Compass
RecruitingNot Applicable
Structured Wii Aerobic Protocol on Reaction Time and Pulmonary Functions in Over Weight School- Aged Children
Egypt60 participantsStarted 2026-03-01
Plain-language summary
Childhood overweight have emerged as major global health concerns and are linked to lower pulmonary functions and reaction time levels among school-aged children. Although exercise, particularly multicomponent training, effectively improves pulmonary functions, maintaining exercise adherence in children with overweight remains a significant challenge. As a result, there is a need for more engaging and motivating exercise options for this group, and active structured wii protocol, which involve full-body movement and boost energy expenditure, have been suggested as a promising alternative..
Who can participate
Age range
10 Years – 15 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* School age children 10-15 years.
* Both gender.
* Diagnosed with over weight with Body mass index (BMI) is at or above the 85th percentile but less than 95th percentile for age , gender and height.
* All participants and parents/guardians were familiar with possible risks associated with the experimental procedures and signed a consent form to participate in the study.
Exclusion Criteria:
* Dysfunction restricting activity, such as neurological disorders.
* Pulmonary disorders such as COPD and malignancy.
* Unstable vital signs.
* Orthopedic problems such as scoliosis and kyphosis.
* Visual and hearing impairments.
* Brain injury
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Forced vital capacity (FVC)
Timeframe: pre and post 36 sessions ( 3 sessions/week ) for 3 months
2
Forced expiratory volume in 1 s (FEV1)
Timeframe: Pre and post 36 sessions ( 3 sessions/week) for 3 months
3
Peak expiratory flow (PEF)
Timeframe: Pre and post 36 sessions ( 3 sessions /week ) for 3 months