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Brain Research and Integrative Neuroscience Network for COVID-19

NCT06517706 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2024-12-06

No results posted yet for this study

Summary

The aim of the experimental study is to investigate two interventions for the management of cognitive symptoms resulting from long COVID. Participants will be randomly assigned into two interventions. 1. Categorization Program (CP) training with active tDCS or 2. Categorization Program training with sham tDCS.

Conditions

  • Cognitive Training
  • Transcranial Direct Current Stimulation

Interventions

COMBINATION_PRODUCT

Combination of tDCS (device) with cognitive training (behavioral)

Participation in 15 one-hour sessions distributed over three weeks. During each session participants will receive two sessions of tDCS plus cognitive training with the Categorization Program

BEHAVIORAL

Categorization Program

Participation in 15 one-hour sessions distributed over three weeks. During each session participants will receive cognitive training and sham tDCS

Sponsors & Collaborators

  • University of Cyprus

    lead OTHER

Principal Investigators

  • Fofi Constantinidou, Ph.D. · University of Cyprus

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
FACTORIAL

Eligibility

Min Age
25 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-15
Primary Completion
2025-10-31
Completion
2025-12-31

Countries

  • Cyprus

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06517706 on ClinicalTrials.gov