This study is completely online and via smartphone and will last 6 weeks. All participants will receive a digital (app-based) treatment for anxiety and worry and will be asked to use the app for 6-weeks. The study will also involve completing 3 phone calls with a study...
For most individuals, active participation in daily life requires the ability to follow conversations in crowded acoustic environments. Most typically-functioning young individuals have little trouble communicating in noisy environments. However, these processes are susceptible to disruption or breakdown at every level of the ascending auditory...
To evaluate the efficacy of troriluzole as adjunctive therapy compared to placebo in subjects with OCD who have had an inadequate response to their current OCD treatment based on the change in their Y-BOCS score To assess the safety and tolerability of troriluzole, relative to placebo,...
To evaluate the efficacy, safety, and tolerability of AVP-786 compared to placebo, for the treatment of agitation in patients with dementia of the Alzheimer's type To evaluate the effects of AVP-786 compared to placebo on neuropsychiatric symptoms To evaluate the effects of AVP-786 compared to placebo on...
To evaluate the clinical efficacy of ATH-1017 To determine the safety and tolerability of ATH-1017 To evaluate the clinical efficacy of ATH-1017 separately on: (1) cognition and (2) clinical global impression of change To evaluate the effect of ATH-1017 on activities of daily living To determine the plasma pharmacokinetic (PK) profile...
To determine if treatment with SAGE-217 reduces depressive symptoms in women with postpartum depression (PPD) compared to placebo. To determine if treatment with SAGE-217 reduces anxiety symptoms compared to placebo. To assess self-report of depressive symptoms To evaluate the safety and tolerability of SAGE-217 This is a PHASE 3...
[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text] Adapt Out COVID is a master protocol to evaluate the safety and efficacy of investigational agents for the treatment of non-hospitalized adults with COVID-19. The trial is a randomized controlled platform that allows agents to be added and dropped...
People working in the food industry (groceries, restaurants, food delivery, factories) during COVID have had a higher risk of getting the illness. Researchers at the University of Washington and Indiana University are interviewing people working in food service, delivery, or provision to understand their work...
This research study is a collaboration between the University of Wyoming and the University of Washington. We are asking you to complete this survey because you are over the age of 65 years. The purpose of this survey is to better understand various health behaviors and...
The University of Washington is conducting a research study called Do More Feel Better for adults aged 60 and older who attend senior centers and are experiencing depression. The program is based on research showing that increasing your participation in pleasurable and rewarding activities can...
