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Intervention study of virtual reality-based exercise and exercise in overweight and obese adolescents

Intervention study of virtual reality-based exercise and exercise in overweight and obese adolescents - Reverie

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068786
Enrollment
Unknown
Registered
2023-02-28
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

overweight and obesity

Interventions

VR soccer group:Added VR soccer training on the basis of the original on-campus physical education class
VR table tennis group:Added VR table tennis training on the basis of the original on-campus physical education classing
Real-world soccer group:Added real world soccer training on the basis of the original on-campus physical education classing
Real-world table tennis group:Added real world table tennis training on the basis of the original on-campus physical education classing
Control group:Maintain the original lifestyle (only on-campus physical education classing)

Sponsors

Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
11 Years to 18 Years

Inclusion criteria

Inclusion criteria: (1) Informed consent of parents and individuals (2) Between 11 and 18 years old (3) Overweight and/or obesity (4) Currently not taking weight-loss drugs and no previous history of bariatric drug use (5) Stable weight (self-reported weight change<5 kg) within 90 days before the screening period

Exclusion criteria

Exclusion criteria: (1) Participate in an organized weight loss program within 90 days before the screening period (2) Currently taking any of the following medications: pramlintide, orlistat, zonisamide, topiramate, lorcaserin, phentermine, bupropion, naltrexone, glucagon-like peptide-1 (GLP-1) receptor agonist, or metformin (used to treat obesity) (3) Have received previous surgical treatment for obesity (4) Damage to tissues and organs such as muscles, bones or nerves (hindering sports training) (5) Non-simple obesity, including endocrine and metabolic diseases (such as Cushing's syndrome, hypothyroidism, hypogonadism, polycystic ovary syndrome, etc.), tumors and trauma (6) History of severe mental illness (such as schizophrenia, bipolar disorder, major depression). (7) Confirmed subjects with bulimia nervosa disorder (8) People who have barriers such as vertigo when using VR (9) Any circumstance which may endanger the safety of the subject or the subject's non-compliance with the protocol

Design outcomes

Primary

MeasureTime frame
Change in body fat mass;

Secondary

MeasureTime frame
Change in body composition;Change in anthropometric indicators;Change in insulin sensitivity;Change in HbA1c;Change in cardiac autonomic neuropathy;Change in exercise-related indicators;Change in appetite;Change in cognitive function;Change in metagenomics;Change in metabolomics;Change in clinical biochemical indexes;Change in intrahepatic triglyceride content;Change in exercise-related indicators;Change in diopter;Changes in the fundus;Changes in the vision;Changes in the olfaction;

Countries

China

Contacts

Public ContactLi Huating

Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

huarting99@sjtu.edu.cn+86 13916502465

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026