MedPath

Immersive Virtual Reality Exergames and Office Workers' Cardiometabolic Health

Not Applicable
Not yet recruiting
Conditions
Exergaming
Metabolic Syndrome
Interventions
Behavioral: 12-week at-home immersive virtual reality exergame
Registration Number
NCT06556784
Lead Sponsor
Guangzhou University
Brief Summary

The worldwide increasing of prevalence of non-communicable diseases has grown the recognition of necessity for identifying the modifiable risk in preventing and managing these diseases. While, the office worker, as a representative group of physical inactivity, is exposed to risk factor of metabolic syndrome which is considered as the pathway of non-communicable diseases. This study mainly focuses on the purpose of examining the interventional efficacy of at-home immersive virtual reality exergame on several metabolic syndrome biomarkers among office workers. In addition, it purposes to determine the impacts of at-home immersive virtual reality exergame on lifestyle pattern of office workers. A 2-armed, single blinded randomized controlled trial (RCT) will be applied to examine the therapeutic effects of at-home immersive virtual reality exergame in this exploratory study. 120 Japanese office workers with less than 150 minutes per week of moderate to vigorous sports activities will be recruited by a convenience sample method. They are randomly allocated to two parallel groups, which including an intervention group: 12-week training of at least 150 minutes per week at-home immersive virtual reality exergame playing with a set device of Meta Quest 2, a control group: 12-week of maintaining regular exercise, eating, and working habits without making significant changes. During this 12-week trial, 3 main follow up steps are included at the timelines of 0 week, 6 weeks, 12 weeks. For each follow up, we will collect three types of variables, including major clinical risk factors of metabolic syndrome, lifestyle pattern factors of metabolic syndrome, and demographics (0 week only). To analysis the variance between intervention group and control group, mixed linear model will be applied to understand the efficacy result of this intervention. The variances of metabolic syndrome clinical risk factors between groups would be used to express the therapeutic effects of at-home immersive virtual reality exergame. The changes of lifestyle pattern factors would be applied to show the impacts of at-home immersive virtual reality exergame on lifestyle pattern.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
120
Inclusion Criteria
  • 18-64 years old
  • Capable of standing and exercising.
  • Having no history of diagnosis of heart disease, cancer, or dementia.
  • Being interested in playing with the exergames.
  • Willingness of adhering to a 12-week interventional exergame treatment.
Exclusion Criteria
  • Individuals who are already engaged in more than 150 minutes per week of moderate to vigorous activities.
  • Individuals with some pharmacological treatments, some surgery (bariatric surgery), and some traditional Chinese medicine.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
12-week at-home immersive virtual reality exergame12-week at-home immersive virtual reality exergame12-week training of at least 150 minutes per week at-home immersive virtual reality exergame playing with a set device of Meta Quest 2 and maintaining regular eating and working habits without making significant changes.
Primary Outcome Measures
NameTimeMethod
HypertensionBaseline (0 week), Mid-follow up (6-week), Final follow up (12-week).

a Systolic blood pressure \> 140 mmHg AND diastolic blood pressure \< 90 mmHg.

Impaired fasting glucoseBaseline (0 week), Mid-follow up (6-week), Final follow up (12-week).

a fasting plasma glucose (FPG) concentration between 6.1 and 6.9 mmol/l.

Body mass indexBaseline (0 week), Mid-follow up (6-week), Final follow up (12-week).

Weight and height will be combined to report body mass index in kg/m\^2.

High-density lipoprotein cholesterol (HDL-C)Baseline (0 week), Mid-follow up (6-week), Final follow up (12-week).

HDL-C concentration less than 35 mg/dl for men (39 mg/dl for women).

Low-density lipoprotein cholesterol (LDL-C)Baseline (0 week), Mid-follow up (6-week), Final follow up (12-week).

LDL-C \< 160 mg/dl

TriglyceridesBaseline (0 week), Mid-follow up (6-week), Final follow up (12-week).

Triglycerides concentration \> 150 mg/dl.

Secondary Outcome Measures
NameTimeMethod
Exercise time (including exergaming time)Baseline (0 week, self estimation), Mid-follow up (1-6 week), Final follow up (7-12 week).

Total minutes of exercise time and exergaming time per week.

Sedentary timeBaseline (0 week, self estimation), Mid-follow up (1-6 week), Final follow up (7-12 week).

Total minutes of sedentary time per week.

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