Feasibility of An Active Video Gaming Intervention

Physical Disability Clinical Trial

Official title:

Feasibility of An Active Video Gaming Intervention to Improve Health and Function in Adults With Mobility Impairments

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05310279
• Other study ID #: IRB-300009049
• Secondary ID: 90REGE000
• Status: Recruiting
• Phase: N/A
• Start date: October 12, 2023
• Est. completion date: November 2024

Study information

• Verified date: June 2024
• Source: University of Alabama at Birmingham
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Replacing sedentary behaviors during leisure time with active video gaming (AVG) has been shown to be an enjoyable option for increasing the amount of physical activity acquired each week. This project will examine the feasibility of an AVG intervention using the GAIMplank.

Description:

Replacing sedentary behaviors during leisure time with active video gaming (AVG) has been shown to be an enjoyable option for increasing the amount of physical activity acquired each week. A growing body of literature indicates that increases in energy expenditure can be achieved during AVG play in people with physical disabilities, including those with mobility impairments such as cerebral palsy (CP), spinal cord injury, stroke, and other neurological conditions. AVGs are particularly important for people with disabilities given the higher rate of inaccessible features in the built environment and the difficulty in finding activities they enjoy. Since AVG devices are relatively affordable, they also hold promise as a scalable product for promoting higher levels of physical activity and fitness among people with disabilities.

There continues to be a pressing need to make gaming controllers accessible to people who are unable to stand for long periods, cannot stand on a small platform due to poor balance or extreme obesity, or who are unable to stand and are full-time wheelchair users. The GAIMplank controller, was developed and tested for usability among people with mobility impairments. During usability testing, a sample of 21 adults were able to successfully access and play a series of standard PC video games using trunk/body movements to produce game play action. Using validated survey tools, participant usability scores and qualitative feedback indicated above average usability for the GAIMplank system. In addition, participants enjoyed the activity and reported game play as light to moderate intensity activity.

This project will examine the feasibility of an AVG intervention using the GAIMplank.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 10
• Est. completion date: November 2024
• Est. primary completion date: July 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18+ years of age

• Self-reported physical disability that limits their mobility

• Communicate in English

Exclusion Criteria:

• Significant impairment in visual acuity that prevents seeing a 52" TV screen to follow exercise

• Body weight >400 lbs

• Cognitive or linguistic problems with understanding instructions or filling in self-administered outcome measures in English as determined by a score of <17 on the telephone-version of the Mini-Mental State Exam

• Any other conditions that would limit ability to play video games

• Cardiovascular disease event within the past 6 months

• Severe pulmonary disease or renal failure

• Currently pregnant

• Ongoing exacerbation of a health condition

Related Conditions & MeSH terms

• Physical Disability

Intervention

Other:
• GAIMplank
The GAIMplank video game controller will be used to play active video games.

Locations

Country	Name	City	State
United States	WHARF	Homewood	Alabama

Sponsors (1)

Lead Sponsor	Collaborator
University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Level of physical activity from baseline to 6 weeks	Instrument physical activity questionnaire - disability (IPAQ-D)	6 weeks
Secondary	Physical activity enjoyment from baseline to 6 weeks	Physical activity enjoyment scale	6 weeks
Secondary	Health-related quality of life from baseline to 6 weeks	SF-36v2	6 weeks