Found 13 ps-center-for-the-neuroscience-of-depression-stress trials
A listing of ps-center-for-the-neuroscience-of-depression-stress medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.
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This study involves 4 study visits over the course of 2 months. You will be asked to track your menstrual cycle (if applicable) and will come in for 3 sessions of TMS and blood draws. Compensation is incremental and corresponds to study participation. Total compensation for the study is $500.FILL …
The research study is being conducted to determine if active VNS (Vagus Nerve Stimulation) Therapy helps depression subjects compared to a no-stimulation control group. This trial has is currently only recruiting bipolar subjects. Patients with an established diagnosis with Treatment-Resistant Depression (TRD), Bipolar I or II, and have been referred …
The research study is being conducted to study brain patterns of negative emotion and develop personalized brain stimulation protocols to disrupt these patterns with transcranial magnetic stimulation (TMS). First, we will use functional Magnetic Resonance Imaging (fMRI) data to generate a negative affect map for each subject. Then, we will …
The research study is being conducted to examine the effects of accelerated intermittent theta-burst stimulation (aiTBS), a form of transcranial magnetic stimulation, to the inferior parietal lobe (IPL) in a sample of BD patients who are currently depressed. This project will recruit patients aged 22-65 with symptoms of bipolar depression …
To test if TMS to MRI-guided cortical targets can create neuronal activity changes in downstream regions of interest To determine if TMS-sEEG is a valid research approach to study circuit engagement and specific connections of deep brain nuclei in the human brain To investigate the effects of clinically relevant TMS …
Objectives 1) Evaluate the safety and feasibility of focused ultrasound to three brain targets Changes in VAS scores, Changes in pre- and post-study imaging, Changes in symptomatic checklist survey data Psychophysiology (heart rate, respiration, skin conductance), Y-BOCS score
This study will evaluate the efficacy and safety of brenipatide vs placebo as an add-on to stable standard of care (SoC) in adults with BD I/II in remission or near remission with residual symptoms. The primary measure is time to relapse. The study includes Screening (~4 weeks), Double-Blind Treatment (until …
The study evaluates the efficacy and safety of brenipatide vs. placebo as an add-on to ongoing MDD treatment. Eligible participants have MDD in remission or near remission with residual symptoms. They will complete a ~4-week Screening period before randomization, followed by a Double-Blind Adjunctive Treatment period until relapse, other discontinuation …
We are requesting a reliance agreement with Advarra for a randomized control trial using the ATTN201 device for the treatment of OCD. The ATTN201 device will provide low-intensity focused ultrasound to the subthalamic nucleus (STN). The device is a safe, easy-to-use, helmet-like device meant to be used in-clinic or at …
The dlPFC is increasingly being targeted with TMS to reduce anxiety expression; however, there is little mechanistic evidence supporting treatment. Thus, the objective of the current project is to develop an interleaved TMS/fMRI that can assess the effect of TMS protocols on neural and behavioral measures related to anxiety expression. …
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