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NCT05582603: CCTLongCOVID

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

Status unknown Phase 1, PHASE2 Last updated 18 October 2022
What this trial tests

Phase 1, PHASE2 trial testing CCT Long COVID in Post-Acute COVID-19 in 20 participants. Status unknown.

Timeline
18 October 2022
Primary endpoint
30 November 2022
30 November 2022

Quick facts

Lead sponsorUniversidad Antonio de Nebrija
PhasePhase 1, PHASE2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date18 October 2022
Primary completion30 November 2022
Estimated completion30 November 2022
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Universidad Antonio de Nebrija

Who can join

Adults 25 to 55, any sex, with Post-Acute COVID-19 or Post Acute COVID-19 Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Post-Acute COVID-19

Currently open trials in the same condition.

Other Universidad Antonio de Nebrija trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05582603.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing