Depression, Pain
Conditions
Brief summary
The overall objective of this study is to determine the feasibility of identifying transdiagnostic biomarkers of cognitive function mediated by neuromodulation of the dorsolateral prefrontal cortex that are translatable across disease groups in order to more accurately phenotype clusters of cognitive dysfunction. Completing behavioral paradigms with electrophysiology and TMS is a challenging frontier. This study focuses on the feasibility of such an endeavor for those with chronic pain or depression as well as healthy controls.
Detailed description
This study aims to test the feasibility of procedures aimed at discovering transdiagnostic biomarkers for cognitive impairment in chronic pain and depression. Fifteen healthy control participants and 15 participants from each disease group (chronic pain, depression) will be recruited. Using a task-based fmri, TMS will be targeted for priming of the Left DLPFC. EEG will be used during our behavioral paradigm to compare changes in DLPFC function before and after primed TMS.
Interventions
N-back, COGED, PacMan game, Bandit task, Websurf task.
Health surveys to study themes like pain, sleep, depression and anxiety, and PTSD.
Sponsors
Study design
Intervention model description
Feasibility study
Eligibility
Inclusion criteria
Arm 1, healthy controls: Inclusion Criteria: * Have access to the online study platform.
Exclusion criteria
* under 18, non-English speaking Arm 2: pain and depression: Inclusion Criteria: * Pain or depression
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Feasibility for all aspects of the study | 1-7 days | Feasibility; the overall objective of this study is to determine the feasibility of identifying transdiagnostic biomarkers of cognitive function mediated by neuromodulation of the dorsolateral prefrontal cortex that are translatable across disease groups in order to more accurately phenotype clusters of cognitive dysfunction. Completing behavioral paradigms with electrophysiology and TMS is a challenging frontier. This study focuses on the feasibility of such an endeavor for those with chronic pain or depression as well as healthy controls. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Acceptability | 1-7 days | Sum total of acceptability rating scale of study procedures. |
Countries
United States