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Evaluation of Exercise Capacity in Teenage Females Using Virtual Reality and Plyometric Workout

Evaluation of Exercise Capacity in Teenage Females With Abdominal Obesity Using Virtual Reality and Plyometric Workout: Randomized Clinical Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07092228
Acronym
VR
Enrollment
100
Registered
2025-07-29
Start date
2025-06-20
Completion date
2026-01-01
Last updated
2025-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Obesity

Keywords

virtual reality, plyometric exercises, abdominal obesity, exercise capacity

Brief summary

to evaluate the efficacy of virtual reality combined with plyometric workout on abdominal obesity in adolescent females

Detailed description

A total sample size of 100 adolescent females will be assigned to the study and will be divided randomly into two study groups, Study Group A and Study Group B, with 50 subjects in each group. Before the start of the protocol (first session) specific parameters will be taken from all assigned adolescent females in the two groups like waist circumference, waist-hip ratio, Body Mass Index, and some pulmonary function tests in the form of inspiratory reserve volume, Expiratory reserve volume, tidal volume, Inspiratory capacity, and vital capacity. Then, study group A underwent an immersive virtual reality technique in addition to plyometric exercise. Study group B was assigned to a treadmill aerobic workout for 10 minutes in addition to plyometric exercises. All mentioned parameters will be measured again after three months of the treatment program

Interventions

DEVICEvirtual reality and plyometric workout

to evaluate exercise capacity in teenage females with abdominal obesity using virtual reality and plyometric workouts

Sponsors

New Ismailia National University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

using computer software

Intervention model description

randomized clinical trial

Eligibility

Sex/Gender
FEMALE
Age
13 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* Body mass index more than or equal to 30 Kg/cm2 * waist circumference more than 80 cm * medical history of polycystic ovarian syndrome * Age from 13 to 18 years

Exclusion criteria

* uncontrolled hypertension * Rheumatoid arthritis * Any respiratory diseases like Asthma and respiratory infections * Osteoprosis

Design outcomes

Primary

MeasureTime frameDescription
waist circumference in centimeter12 weeksAn objective outcome measure, measured by a tap measurement before and after treatment protocol
waist-hip ratio in centimeter12 weeksobjective measure objective outcome measure, measured by a tap measurement before and after treatment protocol
Body mass index (BMI) in kg/m²12 weeksobjective outcome measure, s calculated by dividing an individual's weight in kilograms by the square of their height in meters. For children and adolescents, BMI values are categorized to assess weight status (underweight, healthy weight, overweight, obese
pulmonary function tests by using electronic spirometry12 weeksAn objective outcome measure like Forced Expiratory Volume in one second. It's a key measurement in spirometry tests, helping to assess lung function and diagnose conditions like asthma

Countries

Egypt

Contacts

Primary ContactMohamed AM Abo El Ros
mohamed.aboelros@pt.ninu.edu.eg01206530584
Backup ContactKrols Isak
3530@zuj.edu.jo0781524278

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026