Ignite Creation Date:
2024-05-06 @ 8:16 PM
Last Modification Date:
2024-10-26 @ 3:24 PM
Study NCT ID:
NCT06315894
Status:
RECRUITING
Last Update Posted:
2024-03-18
First Post:
2024-03-15
Brief Title:
Supervised Computerized Active Program for People With Post-COVID Syndrome SuperCAP Study
Sponsor:
Fundación FLS de Lucha Contra el Sida las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
Organization:
Fundación FLS de Lucha Contra el Sida las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
Study Overview
Official Title:
Design and Implementation of a Supervised Computerized Active Program SuperCAP for Improvement of Cognitive Emotional and Functional Status in People With Post-COVID Syndrome SuperCAP Study
Status:
RECRUITING
Status Verified Date:
2024-03
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:
SuperCAP
Brief Summary:
SuperCAP study is a project aimed at designing and implementing an online program for improvement of cognitive emotional and functional status in post-COVID condition
Detailed Description:
SuperCAP study will include 2 stages
Stage 1 will involve the composition of a focus group previous to the effectiveness study development
The work with this focus group will have several aims among them mainly to participate in the design of the intervention program and to provide feedback on the study follow-up
Stage 2 will include the effectiveness study This stage will comprise the initiation of the intervention program study follow-up and dissemination of the results in the end of the project
Two study groups will participate the Intervention Group and the Control Group
The Intervention Group will be comprised by people with post-COVID condition who will follow the intervention program proposed
The Control Group will be comprised by people with post-COVID condition who will not follow the program
Both groups will fulfill the same study participation criteria
The intervention will consist of the follow-up of a distance program via mobiletablet This program will integrate different games and exercises always with the objective of stimulating the cognitive functioning and the emotional status
Stage 1 will involve the composition of a focus group previous to the effectiveness study development
The work with this focus group will have several aims among them mainly to participate in the design of the intervention program and to provide feedback on the study follow-up
Stage 2 will include the effectiveness study This stage will comprise the initiation of the intervention program study follow-up and dissemination of the results in the end of the project
Two study groups will participate the Intervention Group and the Control Group
The Intervention Group will be comprised by people with post-COVID condition who will follow the intervention program proposed
The Control Group will be comprised by people with post-COVID condition who will not follow the program
Both groups will fulfill the same study participation criteria
The intervention will consist of the follow-up of a distance program via mobiletablet This program will integrate different games and exercises always with the objective of stimulating the cognitive functioning and the emotional status
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