• Exploring the Development of the Infant and Fetal Brain

    Official Title Exploring the Connectivity and Functional Organization of the Infant Brain

    Purpose

    The purpose of the study is to investigate how the brain that we are each born with leads to our own unique behavior later in life, and the similarities and differences between maternal and child brains. We are studying infants prenatally and postnatally, following up with them as they grow and develop, and studying their mothers to understand how similar/different they are to their child.

    Could this study be right for you?

    • Infants under 3 years of age, and pregnant persons who are at least 20 weeks pregnant
    • All participants must have no metal implanted in the body
    • Have no significant health conditions or history of serious mental illness
    • Not suffer from a (fear of enclosed spaces)
    • Pregnancies must be without complication.

    Age Range

    Up to 40 years
  • Research Study on Light Sensitivity after Head Injury

    Official Title Effect of Fixation Training with Colored Light Targets on Traumatic Brain Injury-Associated Photophobia

    Purpose

    Researchers at The Ohio State University College of Optometry are seeking individuals with a recent history of head trauma who are experiencing light sensitivity. The goal of this study is to determine if daily 20 minute fixation training sessions using a colored (red or blue) light target affects symptoms of light sensitivity, or alters other measurements of the eyes and vision including pupil response.  

    This study will involve attending five 1-2 hour study visits, occurring every 1.5 months for 6 months. Study visits will include answering questions about eye and health history, completing surveys, reading letters on an eye chart, having the pupils measured in response to flashes of light, measuring the side vision, measuring eye alignment and in some cases focusing ability. Outside of the study visits, participants will also complete daily 20 minute fixation training sessions for 6 months using a colored (red or blue) light target, completed at home between study visits.

    Could this study be right for you?

    • Must be 18 to 80 years old
    • Experienced a head injury 3 or more months ago
    • Current symptoms of light sensitivity
    • Be healthy and have good eye health

    Age Range

    18 - 80 years
  • Assessing Non-invasive Spinal Stimulation to Evaluate its Safety and Effectiveness in Individuals with Spinal Cord Injury

    Official Title ExaStim Upper Limb Pivotal Clinical Validation Study

    Purpose

    The purpose of this study is to evaluate the safety and effectiveness of ExaStim® transcutaneous spinal stimulation on upper extremity function when applied in combination with physical therapy (PT) and/or occupational therapy (OT).

    Participants will be randomized to the stimulation group or a control group. Outcomes will include sensory, motor, and functional tests, as well as questionnaires.

    Could this study be right for you?

    • Aged 22 years or older
    • Traumatic chronic spinal cord injury
    • Level of injury between C2-T2
    • No active implanted medical device for electrical stimulation
    • No Botox for 3 months
    • Have a chronic, traumatic SCI (chronic is >12 months since injury, or 6 months if unchanged symptoms)
    • Has some, but limited upper extremity function
    • BMI <40
    • Cannot be pregnant

    Age Range

    22 years and up
  • A study assessing the impact of a treatment on anxiety and stress in individuals with memory concerns.

    Official Title Treatment of Stress and Anxiety in mild cognitive impairment (MCI)/Mild Alzheimer's Disease and related dementias (ADRD) and their care partners: A Randomized Controlled Trial

    Purpose

    The purpose of this study is to assess the impact of a treatment on anxiety and stress in individuals with memory concerns and those already with a diagnosis of Mild Cognitive Impairment (MCI), Mild Alzheimer's Disease and related dementias. 

    Could this study be right for you?

    The primary participant must:

    • Be at least 60 years of age
    • Have a “care-partner” that is willing to participate in the full program (such as a spouse, child or a good friend)
    • NOT have a terminal illness or severe motor impairment
    • Be able to use a computer and smartphone and read English at the 6th grade level

    The care partner must:

    • Be at least 18 years of age
    • Be able to use a computer and smartphone and read English at the 6th grade level

    Age Range

    60 - 99 years
  • A Study about Retirement from Contact Sports after Concussion

    Official Title Retirement from contact sports after concussion

    Purpose

    The purpose of this study is to learn about the experiences of children and young adults after they stop playing contact sports due to concussion.

    Could this study be right for you?

    • Male and females aged 14-22 years old
    • Retired from contact sports due to prior concussion

    Additionally, a parent may participate if their child enrolls.

    Age Range

    14 - 22 years
  • Buckeye Concussion Knowledge Survey (BUCKS)

    Official Title BUckeye Concussion Knowledge Survey (BUCKS)

    Purpose

    The purpose of this study is to examine health outcomes in former Ohio State University athletes who played a varsity sport during their time at OSU. The objective is to determine whether athletes who sustained a concussion have different health outcomes than those who did not sustain a concussion. Any former OSU varsity athlete can participate in a 20-minute online survey.

    Could this study be right for you?

    • Anyone who has played a varsity sport as an undergraduate student at OSU, and they have now graduated (i.e., OSU athlete alumni). There are no other restrictions in terms of age, sex/gender, type of sport, etc.

    Age Range

    18 years and up
  • A Study about Retirement from Contact Sports after Concussion

    Official Title Retirement from Contact Sports after Concussion

    Purpose

    The purpose of this study is to understand the experiences of children and young adults after medical retirement from contact sports due to concussion(s).

    Participants and their parent(s) will complete online questionnaires (about 10 minutes) at the time of enrollment. You will then be scheduled for an interview (about 30 minutes) by video meeting or phone.

    Could this study be right for you?

    • Children and young adults who have retired from contact sports or other high-risk activities (i.e. dirt bike riding, downhill skiing...) due to prior concussion.  
    • Parents may participate if their child enrolls.

    Age Range

    14 - 22 years
  • A Study about Eye Teaming, Focusing Ability and Quality of Life

    Official Title Development of Patient-Reported Outcome Measures for Children with Concussion-Related and Non-Concussion-Related Non-Strabismic Binocular Vision, Accommodative and Visual Tracking Problems: Phase 1

    Purpose

    The purpose of this study is to assist in development of a new quality of life survey that can be used to learn more about how eye teaming, focusing ability and eye movement problems affect a child’s life.

    Could this study be right for you?

    • Children experiencing eye teaming, focusing, and eye movement problems (with recent concussion or non-concussed)
    • Children with amblyopia (lazy eye) are excluded

    Age Range

    8 - 17 years
  • Clinical Trial Testing if an FDA Approved Medication Changes Stress Responses

    Official Title Orexin Receptor Antagonists as Modulators of Threat Sensitivity in individuals with Alcohol Use Disorder

    Purpose

    The purpose of this study is to see if BELSOMRA, an FDA approved medication that is prescribed to treat insomnia, changes the body’s response to stress. Participation in the study includes 3 or 5 in-person lab visits (depending on randomization), which include EEG and MRI. Nearly all visits are 1.5 hours long, with the exception of one that is 4-5 hours in duration. Visits are flexible and scheduled at your convenience. Participants take the medication (or placebo) for 4 weeks, during which participation is only composed of virtual surveys via a smartphone app.

    The total length of participation in the study is 1.5-2 months depending on scheduling/availability.

    Could this study be right for you?

    Eligibility Criteria:

    • 18-65 years old
    • Generally medically and physically healthy
    • Regular alcohol use

    Exclusion Criteria:

    • Diagnosis of bipolar disorder, schizophrenia, mania, or psychosis
    • Currently pregnant or trying to become pregnant (female)
    • Presence of ferrous-containing metal in the body
    • Inability to tolerate enclosed spaces

    Exclusion Criteria varies, please contact Study Coordinator for more information.

    Age Range

    18 - 65
  • A Study About the Development of Learning in African-American/Black Children

    Official Title Ontogenesis of Categorization; Linking development, mechanisms, and biology

    Purpose

    The purpose of this study is to investigate the early development of attention, learning, and memory during childhood. Participation in this study includes 4, 90-minute-long visits to the lab per year. During these visits, your child will play 2-3 fun, computerized games. These games are designed to assess various aspects of their cognitive ability. 

    The duration of the study will last 4 years.

    Could this study be right for you?

    Eligibility Criteria: 

    • African-American/Black children who are 4 years old 

    Age Range

    4 - 4