Clinical Trials Directory

Trials / Completed

CompletedNCT04944147

Cognitive Training and Brain Stimulation in Patients With Post-COVID-19 Cognitive Impairment

Neuromodulation Through Brain Stimulation-assisted Cognitive Training in Patients With Post-COVID-19 Cognitive Impairment

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
University Medicine Greifswald · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is to investigate effects of brain stimulation-assisted cognitive training in patients with persistent subjective or objective cognitive impairment after polymerase chain reaction (PCR)-positive COVID-19 disease.

Detailed description

Long-term persistent symptoms occur in a substantial number of patients diagnosed with coronavirus 2019 disease (COVID-19). First evidence suggests that long-term symptoms develop not only after severe courses of the disease, but also after less serious illness and include various symptoms such as fatigue and impaired memory, concentration or sleep. During recovery, these symptoms present a heavy burden for patients, who then often experience psychological distress and reduced quality of life. The goal of the present study is to assess the effects of cognitive training alone or in combination with tDCS on cognitive performance, quality of life and mental health in patients with subjective or objective cognitive impairments following post-COVID disease. Patients will either participate in a three-week cognitive training with concurrent online high-definition tDCS application or placebo ("sham") tDCS or participate in an evidence-based muscle relaxation training combined with placebo tDCS. We hypothesize that cognitive training with sham or active tDCS will result in more pronounced improvement on a transfer task compared to the control group. We also hypothesize that training combined with anodal tDCS will lead to significantly higher performance on a transfer task than training combined with sham tDCS. Additionally, we will determine effects on specifically trained and other untrained cognitive functions immediately after the intervention as well as their maintenance one month later.

Conditions

Interventions

TypeNameDescription
DEVICEAnodal tDCSAnodal transcranial direct current stimulation (tDCS), 9 sessions with 20 minutes stimulation each (2 mA)
DEVICESham tDCSSham transcranial direct current stimulation (tDCS), 9 sessions with 30 sec stimulation each (2 mA) to ensure blinding of participants
BEHAVIORALIntensive cognitive trainingIntensive cognitive training of a letter memory updating task, 9 sessions
BEHAVIORALProgressive muscle relaxation (PMR)Standardized instructed PMR training, 9 sessions

Timeline

Start date
2022-01-05
Primary completion
2024-09-09
Completion
2024-10-08
First posted
2021-06-29
Last updated
2024-12-05

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT04944147. Inclusion in this directory is not an endorsement.