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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age13-18
SponsorNew Ismailia National University

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

uncontrolled hypertension

Rheumatoid arthritis

Any respiratory diseases like Asthma and respiratory infections

Osteoprosis

Trial design

Design model

Crossover

Treatments tested in this trial

  • virtual reality and plyometric workout

    Device

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

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Virtual Reality and plyometricsExperimental treatment 1 intervention
Group B: Treadmill and plyometricExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

waist circumference in centimeter

An objective outcome measure, measured by a tap measurement before and after treatment protocol

Time frame
12 weeks
2

waist-hip ratio in centimeter

objective measure objective outcome measure, measured by a tap measurement before and after treatment protocol

Time frame
12 weeks
3

Body mass index (BMI) in kg/m²

objective 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

Time frame
12 weeks
4

pulmonary function tests by using electronic spirometry

An 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

Time frame
12 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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