Quality of Life Variations Among Adolescent Females Following Virtual Reality Games Approach (NCT06604429) | Clinical Trial Compass
CompletedNot Applicable
Quality of Life Variations Among Adolescent Females Following Virtual Reality Games Approach
Egypt100 participantsStarted 2023-10-01
Plain-language summary
to compare the effects of virtual reality games, aerobic exercise, and dietary modifications on Quality of Life among adolescent females.
Who can participate
Age range
12 Years – 17 Years
Sex
FEMALE
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:
* Obese adolescent girls
* Class I Obesity (Body Mass Index from 30 to 34.99 kg/m2)
* Have regular menstruation
* Clinically and medically stable
* no impairment of sensation or other neurological or psychological problems
Exclusion Criteria:
* Visual and/or auditory defects
* Normal weight girls (Body Mass Index from 18 to 24.99 kg/m2) or below average weight (BMI less than 18 kg/m2) or Class II \& III Obesity (BMI above 35 kg/m2)
* Girls with significant tightness and/or fixed deformity of lower limbs
* Participants with neurological disorders that affect balance or mentality (e.g. epilepsy).
* Girls with advanced radiographic changes include: Bone destruction, Bony ankylosis, Knee joint subluxation, and Epiphysial fracture)
* Congenital or acquired lower limb deformities in the lower limbs.
* Cardiopulmonary dysfunction.
* Girls under insulin therapy, uncontrolled bronchial asthma, anemia, and Pathological causes of obesity (endocrinal, genetic syndromes...etc.).
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
Body mass index
Timeframe: From enrollment to the end of treatment at 8 weeks
2
Fat Mass
Timeframe: From enrollment to the end of treatment at 8 weeks
3
Body Water Content
Timeframe: From enrollment to the end of treatment at 8 weeks
4
Muscle mass
Timeframe: From enrollment to the end of treatment at 8 weeks
5
Waist Circumference
Timeframe: From enrollment to the end of treatment at 8 weeks
6
Waist hip ratio
Timeframe: From enrollment to the end of treatment at 8 weeks
7
Borg Scale (rate of perceived exertion)
Timeframe: From enrollment to the end of treatment at 8 weeks