Evaluation of Exercise Capacity in Teenage Females Using Virtual Reality and Plyometric Workout
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In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: virtual reality and plyometric workout.
- Who it may be relevant to
- Registry conditions: Abdominal Obesity. Basic parameters: 13 years — 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluation of Exercise Capacity in Teenage Females With Abdominal Obesity Using Virtual Reality and Plyometric Workout: Randomized Clinical Trial
Overview
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
- Device virtual reality and plyometric workout
to evaluate exercise capacity in teenage females with abdominal obesity using virtual reality and plyometric workouts
Primary outcome measures
- waist circumference in centimeter [Time frame: 12 weeks]
- waist-hip ratio in centimeter [Time frame: 12 weeks]
- Body mass index (BMI) in kg/m² [Time frame: 12 weeks]
- pulmonary function tests by using electronic spirometry [Time frame: 12 weeks]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Mohamed — Ismailia
Identifiers
NCT: NCT07092228 · IRB # 3/6/2024- 2025