Attention, Memory and Quality of Life in Post-COVID-19 Adults

NANot yet recruitingINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

June 10, 2025

Primary Completion Date

October 31, 2025

Study Completion Date

December 31, 2025

Conditions
Post-Acute COVID-19 SyndromeLong COVIDBrain Fog
Interventions
BEHAVIORAL

qEEG-neurofeedback

The participants will be submitted to a qEEG-neurofeedback intervention in order to verifify its feasibility to enhance cognition. The theta/beta ratio reduction protocol at electrodes Fp1, Fp2, Fz, F3, F4, Cz, C3, C4 will be performed, with 10 sessions of qEEG-neurofeedback training, 2 sessions for pre and post test, and 1 session for follow-up after 30 days of intervention. Each session will last approximately 1 hour. The Psychological Battery of Attention 2 (BPA-2) and Digit Span Test will be employed to measure attention and working memory levels. The Montreal Cognitive Assessment (Moca) will be used for neurological and cognitive assessment. Participants will receive feedback based on their theta/beta ratio in the frontal and central cortical areas (electrodes Fp1, Fp2, Fz, F3, F4, Cz, C3, C4).

BEHAVIORAL

SHAM qEEG-neurofeedback

The participant will be submitted to an inactive qEEG-neurofeedback that appears to be the same as a functional procedure or device. Participants will not receive feedback based on their theta/beta ratio in the frontal and central cortical areas (electrodes Fp1, Fp2, Fz, F3, F4, Cz, C3, C4).

Trial Locations (1)

59.288-899

Santos Dumont Institute, Macaíba

All Listed Sponsors
collaborator

Santos Dumont Institute

OTHER

lead

Jade Carvalho Da Silva

OTHER

NCT07005921 - Attention, Memory and Quality of Life in Post-COVID-19 Adults | Biotech Hunter | Biotech Hunter