Clinical Trials Directory

Trials / Completed

CompletedNCT04573569

Neural Correlates of Cognition and Mood

Status
Completed
Phase
Study type
Observational
Enrollment
30 (actual)
Sponsor
University of Minnesota · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The overall objective of this study is to determine the neural correlates of cognition and mood. This study represents the first preliminary study to begin investigating cognitive and emotional states in patients who have undergone implantation of invasive electrodes for the purpose of seizure localization. In the post-implantation paradigm where patients remain under close supervision with intracranial instrumentation for recording, this study aims to create the platform and preliminary data to inform a larger study for calibrated examination of neural correlates of cognition and mood. As such, this study has the following specific aims: Aim 1: Establish a portable platform for the assessment of cognitive, behavioral, and emotional tasks with time synchronization to ECoG/SEEG recording platform Aim 2: Quantify the variance in clinical assessments of mood and cognitive function in patients undergoing phase II epilepsy monitoring Aim 3: Assess the relationship between validated surveys/tasks and electrophysiology

Detailed description

Study interventions are limited entirely to validated surveys completed on a computer or tablet PC, as outlined above. Patients may elect to have electrodes to be implanted that are not used in standard-of-care at this institution, but are FDA-approved for the same indications. Patients who consent and complete enrollment will be asked to complete cognitive and behavioral tasks on a portable computer or tablet PC while the invasive electrodes remain implanted. Tasks typically require the patient to think or act and then respond by interacting minimally with the portable computer. The primary outcome for this study includes percentage of completed cognitive or behavioral tasks as a measure of the feasibility of the administration of these tasks. As this is a feasibility study, we are interested in the practical aspects of data acquisition. Secondary outcomes include the cognitive and behavioral tasks themselves and their relationship with electrophysiology.

Conditions

Interventions

TypeNameDescription
BEHAVIORALBehavioral testingPatients recruited for this study have already undergone surgical implantation of invasive electrodes for purpose of localizing and characterizing electrographic seizures as part of the second phase of surgical epilepsy evaluation. Patients who consent and complete enrollment will then be asked to complete cognitive and behavioral tasks on a portable computer or tablet PC while the invasive electrodes remain implanted. Tasks typically require the patient to think or act and then respond by interacting minimally with the portable computer. These tasks are performed at the will of each patient during their stay in the intensive care unit while surgical electrodes remain.

Timeline

Start date
2018-03-28
Primary completion
2019-06-30
Completion
2019-06-30
First posted
2020-10-05
Last updated
2022-09-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04573569. Inclusion in this directory is not an endorsement.