Viewing Study NCT06463730



Ignite Creation Date: 2024-07-17 @ 12:07 PM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06463730
Status: COMPLETED
Last Update Posted: 2024-06-21
First Post: 2024-04-18

Brief Title: Comparison Between Custom and Non-custom Serious Games Poststroke
Sponsor: University Rehabilitation Institute Republic of Slovenia
Organization: University Rehabilitation Institute Republic of Slovenia

Study Overview

Official Title: Comparison of Activity Intensity Performance and Users Experience Between Custom and Non-custom Serious Games Combined With Balance Boards for Persons After Stroke
Status: COMPLETED
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SeriousGames
Brief Summary: Serious games for rehabilitation are delivered through systems that are either customised or non-customised Custom serious games allow for control of feedback setting of game speed and difficulty while non-custom games are less adaptable but provide attractive graphics and sounds The study compared the activity intensity and user experience of persons after stroke while playing custom and non-custom virtual reality balance games that were both game- and self-paced
Detailed Description: Persons in chronic phase poststroke will play 12 games 6 self- and 6 game-paced games over two sessions in randomised order Within each game-type custom and non-custom games will be played in random order All games will be played on a balance board whereby each pair of a custom and non-custom game will require comparable movement directions of the center of pressure The custom system will be compared to the non-custom system in terms of number of repetitions movement amplitude users enjoyment flow state likeability and perception of exertion

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None