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Over WeightNCT07513298

Structured Wii Aerobic Protocol on Reaction Time and Pulmonary Functions in Over Weight School- Aged Children

A study testing The Nintendo Wii Fit operates on the Wii system, produced by Nintendo Co., Ltd, based in Kyoto, Japan. and Chest physical therapy and diet therapy in people with Over Weight and School Age Children, run by Al-Zaytoonah University of Jordan at 1 site in Egypt.

Recruiting

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

Sites and contacts
Official record
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Trial 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… Read more about this study

Who is it for?
Ages 10 to 15 yearsHealthy volunteers can take part
Conditions the study is for
Over Weight, School Age Children
What is being tested?
The Nintendo Wii Fit operates on the Wii system, produced by Nintendo Co., Ltd, based in Kyoto, Japan. and Chest physical therapy and diet therapy
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteEgypt
Study dates
1 Mar 2026to Jun 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 10 to 15 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • 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.

Who cannot join

  • 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

Trial locations and contacts

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

Egypt1 site, 1 recruiting
  • Outpatient Clinics of Universities and Private Medical Centers in Cairo

    Cairo, 11571

    Mohamed Zidan, 01016469801, drmohzidan2015@gmail.com

    Recruiting

Other trials in Egypt

About this study

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..

Read the detailed description

Wii Fit aerobic training produces effects similar to standard rehabilitation treatments and requires low energy. This shows that it may be an effective rehabilitation technique for adults and older people with low energy levels. A review found that video games are safe and practicable in children with lung is sues. The principle of this training is that aerobic exercise en hances pulmonary adaptation by increasing the strength and endurance of the respiratory muscles. Altered aerobic training due to endurance training might diminish smooth muscle tone in the airways and enhance expiratory flow. Regular lung stretching caused by airway smooth muscle diminishes airway resistance during aerobic exercise. Reduced tone and smooth muscle contraction may reduce air resistance. As smooth mus cle tone diminishes, airway resistance decreases, and lung vol ume falls, these mechanisms are anticipated to enhance airflow

Being tested
The Nintendo Wii Fit operates on the Wii system, produced by Nintendo Co., Ltd, based in Kyoto, Japan., Chest physical therapy and diet therapy
Keywords
over weight, Wii protocol, pulmonary functions, reaction time, school age children

What participants receive

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

  • The Nintendo Wii Fit operates on the Wii system, produced by Nintendo Co., Ltd, based in Kyoto, Japan.Device

    The Nintendo Wii Fit operates on the Wii system, produced by Nintendo Co., Ltd, based in Kyoto, Japan. Among its features is a collection of interactive video games that require players to embody their on-screen character using a compact, wireless controller capable of motion detection.

  • Chest physical therapy and diet therapyOther

    Chest Physiotherapy:

    Breathing exercises (diaphragmatic breathing, segmental breathing) Incentive spirometry (if applicable) Thoracic expansion exercises

    Diet therapy :

    Individualized calorie-controlled diet plan

Study groups in NCT07513298
Study groupRoleWhat they receive
Chest physical therapy and diet therapyActive comparatorSchool age children who will receive routine chest physical therapy and diet therapy
Receives: Other: Chest physical therapy and diet therapy
Chest physical therapy along with wii aerobic exercises and diet therapyExperimentalSchool age children who will receive routine chest physical therapy along with wii aerobic exercises and diet therapy
Receives: Device: The Nintendo Wii Fit operates on the Wii system, produced by Nintendo Co., Ltd, based in Kyoto, Japan.; Other: Chest physical therapy and diet therapy

What is being measured

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

  1. Forced vital capacity (FVC)

    The maximum amount of air expired after the maximum Inspiration in liters.

    Measured: pre and post 36 sessions ( 3 sessions/week ) for 3 months

  2. Forced expiratory volume in 1 s (FEV1)

    The air volume expired in the first second after maximal Inspiration in liters.

    Measured: Pre and post 36 sessions ( 3 sessions/week) for 3 months

  3. Peak expiratory flow (PEF)

    Achieving maximum forced expiration without hesitation from the point of peak lung inflation yields the maximum expiratory flow

    Measured: Pre and post 36 sessions ( 3 sessions /week ) for 3 months

Secondary outcomes (1)
  1. Chest Expansion

    Upper chest expansion (2nd intercostal space) \& Lower chest expansion (xiphoid) were assessed from the reference point mentioned by using tab

    Measured: Pre and post 36 sessions ( 3 sessions / week ) for 3 months

Timeline

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

  1. First posted7 Apr 2026
  2. Study start1 Mar 2026
  3. Primary completion1 Jun 2026 (estimated)
  4. Study completionJun 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
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Care provider
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07513298
Sponsor's protocol ID
Wii aerobic on reaction time
Status last verified
Apr 2026
First submitted
27 Mar 2026
Last updated
7 Apr 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 The Nintendo Wii Fit operates on the Wii system, produced by Nintendo Co., Ltd, based in Kyoto, Japan. and Chest physical therapy and diet therapy in people with Over Weight and School Age Children, run by Al-Zaytoonah University of Jordan 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 4 inclusion and 6 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: looking for participants now, as of the sponsor's last update on 7 Apr 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?

This study is still under way. Results are not available in the source record yet.

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

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Forced vital capacity (FVC) (time frame: pre and post 36 sessions ( 3 sessions/week ) for 3 months). The study lists 3 primary outcomes in all. 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 7 Apr 2026.

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