Safety and Dosage of a Computerized Cognitive Training Program for Cognitive Dysfunction After COVID-19

Phase 1

Not yet recruiting

• Conditions: Cognitive Impairment; Post Acute COVID-19 Syndrome; Cognitive Dysfunction; Post-Acute COVID-19
• Interventions: Behavioral: CCT Long COVID

• Registration Number: NCT05582603
• Lead Sponsor: Universidad Antonio de Nebrija

Brief Summary

The goal of this Phase I/II clinical trial is to assess the safety and maximum tolerated training time of a self-administered computerized cognitive training (CCT) in individuals with cognitive dysfunction as a consequence of COVID-19 infection.

Detailed Description

A Phase I/II protocol is designed to determine the safety of a Computerized Cognitive Training (CCT) aimed at ameliorating the cognitive dysfunction often observed in persons with post-acute sequelae of COVID-19 (PASC). The Phase I/II trial also aims at establishing the maximum tolerated training time per session of the CCT and to explore the feasibility of such intervention. In Phase I, through a 3+3 design, a dose-escalation trial will be set. Participants will be tested across subsequent training blocks of 15 minutes each, reporting on the experienced fatigue or adverse effects after every block. The safe training dose will be set to a block before extreme fatigue or a notable adverse effect has been reported by two or more participants. Once a safety training time has been established, a group of participants will engage in a 15-day training effectiveness assessment. After an initial thorough pre-test assessment, the intervention protocol will start. An evaluation day and a training day will be interspersed so that participants will complete a total of 8 training sessions (days 1, 3, 5, 7, 9, 11, 13 and 15). After the final day of intervention, a post-test assessment session will be carried out.

Study Timeline

• Status Verified: 2022-10
• Study First Submitted: 2022-10-13
• Study First Submitted QC: 2022-10-13
• Last Update Submitted: 2022-10-16
• Study First Posted: 2022-10-17
• Study Start: 2022-10-18
• Last Update Posted: 2022-10-18
• Primary Completion: 2022-11-30
• Study Completion: 2022-11-30

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Adults between 25 and 55 years old.
• History of infection with COVID-19 at least 3 months prior to expression of interest with a valid diagnostic or antibody test.
• Presence of self-perceived cognitive dysfunction associated with post-acute sequelae of COVID-19 (concentration problems or brain fog).

Exclusion Criteria

• Suicidal traits.
• Poor digital skills.
• Not having access to a mobile phone or tablet with Internet connection during the time of the intervention (only for Phase II).
• Not having 60 spare minutes per day to complete the intervention (only for Phase II).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Computerized Cognitive Training	CCT Long COVID	Individuals enrolled in Phase I and II will complete a Computerized Cognitive Training (CCT) based on an intervention with 15 different cognitive tasks in the form of games aimed at enhancing memory, attention, reasoning, perception and coordination skills. The CCT will be implemented in an app designed by CogniFit (CogniFit Inc., San Francisco, USA) to be used in tablets or mobile phones.

Primary Outcome Measures

Name	Time	Method
Fatigue Level Questionnaire	In Phase II, on even days (rest days of the intervention protocol).	Fatigue questionnaire adapted from the Brief Fatigue Inventory (Mendoza et al., 1999)
Safety Level Questionnaire	In Phase II, on even days (rest days of the intervention protocol).	Safety questionnaire aimed at exploring the existence of side effects and/or adverse events.
Classification of side effect or adverse events	In Phase II, on even days (rest days of the intervention protocol), only in case side effects or adverse events have been reported in the Safety Questionnaire.	Interview adapted from the Patient-Reported Adverse Drug Event Questionnaire (de Vries et al., 2013).

Secondary Outcome Measures

Name	Time	Method
Quality of Life Assessment	In Phase II, at pre-test (the day before the intervention protocol starts) and at post-test (the day after the intervention protocol finishes).	Short version of the self-perceived global physical and mental health scale from the Patient-Reported Outcomes Measurement Information System (PROMIS v.1.2).
Computerized Cognitive Assessment	In Phase II, at pre-test (the day before the intervention protocol starts) and at post-test (the day after the intervention protocol finishes).	Complete cognitive evaluation based on Cognitive Assessment Battery (CogniFit Inc., San Francisco, USA).
Paper-and-pencil Cognitive Assessment	In Phase II, at pre-test (the day before the intervention protocol starts) and at post-test (the day after the intervention protocol finishes).	The Montreal Cognitive Assessment (MoCA).

Trial Locations

Locations (1)

Universidad Nebrija; 🇪🇸 Madrid, Spain