Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06526975
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
None
First Post:
2024-07-15
Brief Title:
Study of Different Exercise Doses Through Videogames in Older Adults
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Study of Different Exercise Doses Through Digital Gamification in Older Adults
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The objective of this clinical trial is to assess the feasibility of applying different gamified exercises doses in older adults It will also learn from possible adverse effects of the intervention
The main questions this clinical trial aims to answer are
Are there any differences between heart rate perceived exertion and enjoyment between groups
Are there any adverse effects What is the magnitude of these adverse effects
Are there any correlations between gamification time and the occurrence of adverse effects
The main questions this clinical trial aims to answer are
Are there any differences between heart rate perceived exertion and enjoyment between groups
Are there any adverse effects What is the magnitude of these adverse effects
Are there any correlations between gamification time and the occurrence of adverse effects
Detailed Description:
A randomised clinical trial will be conducted in which the use of exercise doses between 10 and 30 will be tested Participants will be recruited from Nueva Esperanza nursing home Fuensalida Toledo The study will be conducted according to the CONSORT statement for clinical crossover and parallel trials
The study will have a total of two experimental groups with different intervention times between 10 and 30 minutes respectively using a mobile application The intervention will consist of performing exercise in pairs in a single bout during the mentioned times
The study will have a total of two experimental groups with different intervention times between 10 and 30 minutes respectively using a mobile application The intervention will consist of performing exercise in pairs in a single bout during the mentioned times
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None