The purpose of this study is to explore the physicians’ knowledge of intellectual disabilities (ID) and their medical training and practice. The information resulting from this study will help to design adequate interventions and training programs for medical students and physicians aimed to improve their ID knowledge and the health care services provided to patients with ID.

This is an observational cross-sectional study of physicians in the US using an anonymous online survey. The entire survey has 156 items and will require 15-20 minutes to complete.

This is a study is being done to find out if a phone app reduces calling and texting while driving among young drivers.

The purpose of this research study is to evaluate the drug Levomilnacipran extended-release to see how well the drug works, observe the side effects, and how well tolerated it is compared to placebo in pediatric patients with major depressive disorder.

The overall objective is to investigate to investigate how safe, how well tolerated, and how effective R3R01 is in treating uncontrolled proteinuria in patients with Alport syndrome and steroid-resistant Focal Segmental Glomerulosclerosis.

All eligible participants will be enrolled to receive R3R01 over a treatment period of 12 weeks. The study will consist of 3 periods, including a screening period of 3 weeks, a treatment period of 12 weeks, and a follow up of period of 12 weeks.

The purpose of this study is to determine the best way to help people that have had a kidney transplant perform daily physical activity. Currently, we do not know the best way to help people who have had a kidney transplant to remember to perform regular physical activity. This study will help us explore how to promote routine daily physical activity

The purpose of this study is to examine whether active VNS Therapy treatment is superior to a no stimulation control in producing a reduction in baseline depressive symptom severity, based on multiple depression scale assessment tools at 12 months from randomization.

The duration of the study will consist over a 5 year period. You will visit the study site approximately 23 times after your implant surgery.

The purpose of this registry is to collect information about Hypophosphatasia (HPP), a rare bone disorder characterized by the abnormal development of bones and teeth. This long-term registry will collect and store patient medical information, and other related information to use in medical research. the registry may help researchers better understand the condition and learn more about patients who have HPP. This data may help other people with HPP in the future.

This research study will look at how patterns of brain activity influence thoughts and behaviors. This research is being done to better explain why people have thoughts about suicide and how different suicide prevention strategies impact brain responses to emotional information.

The purpose this study is to examine how individual differences in health changes (muscle strength, blood pressure) and behavioral changes (sleep, physical activity) impact memory, attention, and the brain. We study these relationships in among a variety of older adults, including those with a history of concussion, traumatic brain injury (TBI), and posttraumatic stress disorder (PTSD).

The long-term goal of this project is to identify modifiable factors that exacerbate or protect from age-related cognitive decline.

Femoroacetabular impingement syndrome (FAIS), also known as hip impingement, is the most common cause of debilitating hip pain in young, active adults. FAIS is a movement-related syndrome defined by bony structure, clinical signs, and symptoms.

The purpose of this study is to better understand how muscle strength and timing of muscle activation contribute function and symptoms in hip impingement.  

You will be in the study for one day. The time involved in the clinical exam, laboratory testing session, and surveys will take a maximum of 2-3 hours. 

The overall goal of this study is to examine whether after a C-Section delivery, the use of non-invasive bioelectronic treatment (treating women with devices that balance electrical signaling in the nervous system) will help improve pain management and reduce inpatient postoperative opioid use.

Your participation in this study will last 6 weeks. You will be asked to complete a series of questions at the end of your enrollment.

The purpose of this study is to examine how men and women with dementia and/or cancer might process and respond to pain or discomfort.

Participants may complete various questionnaires by phone or video conferencing once a week for up to 7 weeks with one optional in-person session.