Clinical Trials Directory

Trials / Completed

CompletedNCT06315894

Supervised Computerized Active Program for People With Post-COVID Syndrome (SuperCAP Study)

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
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

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 mobile/tablet. This program will integrate different games and exercises always with the objective of stimulating the cognitive functioning and the emotional status.

Conditions

Interventions

TypeNameDescription
DEVICESuperCAP ProgramDistance program including tasks and exercises to improve cognitive, emotional, and functional status. The intervention will be applied via cell phone and will have a duration of 3 months (12 weeks). Tasks and exercises will be performed 5 days per week. Contents of the program will include daily exercises, daily games, daily videos, and weekly videos. They will address cognitive functions, daily habits, and lifestyle factors in general. Compliance will be monitored to control the adherence to the intervention. The program has been designed specifically for people with post-COVID syndrome.

Timeline

Start date
2023-10-03
Primary completion
2024-09-05
Completion
2024-09-05
First posted
2024-03-18
Last updated
2025-12-30

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT06315894. Inclusion in this directory is not an endorsement.