Research studies are looking for volunteers just like you. Both healthy volunteers and participants with specific health conditions are needed to help answer important questions impacting the health of our friends and family. Join us to improve the health of others.

Study Categories

  • A Study to Evaluate Baricitinib in Adult Patients with Severe or Very Severe Alopecia Areata

    Official Title
    A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Operationally Seamless, Adaptive Phase 2/3 Study to Evaluate the Efficacy and Safety of Baricitinib in Adult Patients with Severe or Very Severe Alopecia Areata BRAVE-AA1
    Purpose

    The purpose of this study is to evaluate the efficacy of baricitinib.

    Could this study be right for you?
    • Subject must self-identify as Black or African American 
    • Subject's current episode of alopecia areata must be more than 6 months and no longer than 8 years
    • Subject must not have any spontaneous improvement 
    • Subject must be in good general health with no history of tuberculosis, heart disease, cancer, HIV, hepatitis B or C, or blood clots 
    • Female subjects must not be pregnant, breastfeeding, or considering becoming pregnant for the duration of the study 
    Age Range
    18 years and up
  • A Study to Evaluate Rocatinlimab in Adults with Atopic Dermatitis (Ezcema)

    Official Title
    A Phase 3, Randomized, 24-week, Placebo-controlled, Double-blind Study to Assess the Efficacy, Safety and Tolerability of Rocatinlimab (AMG 451) Monotherapy in Adult
    Subjects With Moderate-to-severe Atopic Dermatitis (AD) (ROCKET-Horizon)
    Purpose

    The purpose of this study is to evaluate the efficacy of rocatinlimab. 

    Could this study be right for you?
    • Subject must have a diagnosis of atopic dermatitis for a least 6 months prior to study visit
    • Subject must have tried a topical medication with little to no improvement
    • Subject must be in good general health with no history of tuberculosis, heart disease, cancer, HIV, hepatitis B or C, or blood clots 
    • Female subjects must not be pregnant, breastfeeding, or considering becoming pregnant for the duration of the study 
    Age Range
    18 years and up
  • A Study to Evaluate Povorcitinib in Adults with Hidradenitis Suppurativa (HS)

    Official Title
    A Phase 3, Double-Blind, Randomized, Placebo-Controlled, Efficacy and Safety Study of Povorcitinib (INCB054707) in Participants With Moderate to Severe Hidradenitis Suppurativa
    Purpose

    The purpose of this study is to evaluate the efficacy of povorcitinib.

    Could this study be right for you?
    • Subject must have a diagnosis of hidradenitis suppurativa for at least 3 months prior to study visit 
    • Subject must have at least 5 active HS spots in 2 different body areas 
    • Subject must have tried an oral or injected medication for HS with little to no improvement 
    • Subject must be in good general health with no history of tuberculosis, heart disease, cancer, HIV, hepatitis B or C, or blood clots 
    • Female subjects must not be pregnant, breastfeeding, or considering becoming pregnant for the duration of the study 
    Age Range
    18 years and up
  • Eye Tracking of Pitched Balls

    Official Title
    Gaze tracking of pitched balls - bat swing versus passing height judgments
    Purpose

    The purpose of this study is to compare eye and head movement behavior when baseball batters swing at (but do not hit) an approaching ball and when batters judge the height above the ground at which an approaching ball would reach had it arrived at the batter.

    Could this study be right for you?
    • Must have visual acuity of 20/20 in each eye
    • No eye turn
    • Depth perception of 60 seconds of arc
    • Must have played organized baseball or softball at the high school level or above within the last 10 years
    Age Range
    18 - 40 years
  • Impact of A Low Glycemic Index Diet on Blood Pressure and Blood Sugar in Individuals with Spinal Cord Injury

    Official Title
    Two Birds with One Stone: Impact of A Low Glycemic Index Diet on Postprandial Hypotension and Glucose Metabolism in Individuals with Spinal Cord Injury (FIP)
    Purpose

    The purpose of this study is to examine the effect of a short-term low glycemic index diet on blood pressure and blood sugar control after eating.

    Could this study be right for you?
    • Adults aged 18-65 years old
    • Chronic spinal cord injury
    • Level of injury between C4 and L2
    Age Range
    18 - 65 years
  • Brains, Emotion Regulation and Adolescent Moods (BEAM) Study

    Official Title
    Neurodevelopmental Mechanisms Underlying the Onset of Depression among At-Risk Youth: The Role of Dysregulation in the Negative Valence System
    Purpose

    The purpose of this study is to test whether changes in the way in which we react and respond to emotional or stressful information represent a risk factor for depression in kids of mothers with and without depression. Findings from the study have the potential to decrease the high rates of depression observed in children of depressed mothers.  

    Could this study be right for you?

    You may be eligible for this study if:

    • You are 18-65 years old and female.
    • You have a biological child who is between 9 and 14 years of age.
  • Understanding Patient Experiences of Gestational Diabetes

    Official Title
    A Multi-Actor Examination of Gestational Diabetes Mellitus (GDM)
    Purpose

    This study aims to examine the experience of people who have been diagnosed or are currently living with gestational diabetes, including how they manage and make sense of their diagnosis. 

    Could this study be right for you?
    • Aged 18 years or older
    • Must live in the state of Ohio
    • Must be currently pregnant and have been diagnosed with gestational diabetes OR must have been diagnosed with gestational diabetes during a recent pregnancy (within the last 12 months)
    Age Range
    18 years and up
  • A Study for Active Military Service Members (or recently served); Examining Uncertainty, Health, and Home Safety Practices

    Official Title
    Uncertainty and Firearms: Obtaining Secure Storage (UFOS)
    Purpose

    The purpose of this study is to examine whether fear of uncertainty plays a role in home safety practices among firearm owners who are currently or have recently served in the U.S. military.

    Could this study be right for you?
    • Currently serving in any Branch or Component of the U.S. military, or were discharged from the U.S. military within the past 90 days
    • 18 years or older
    • Own at least one firearm located in your home or vehicle
    • Are able to speak and understand the English language
    • Have an Apple or Android smartphone 
    Age Range
    18 - 99 years
  • Research Study on Aging and Health after Cancer

    Official Title
    E-PROOF: E-intervention for Protein Intake and Resistance Training to Optimize Function
    Purpose

    Our team is looking to improve the health of older cancer survivors after they have completed cancer treatment. Specifically, this 12-week study looks to improve older cancer survivors' physical function and related health outcomes (muscle strength, dietary quality, health-related quality of life, self-efficacy, weight management). 

    Could this study be right for you?

    -History of stage I-III breast, colorectal, and prostate cancer

    -Completion of curative treatment (chemotherapy, radiation, surgery)

    -Have an email address

     

    Age Range
    65 years and up
  • A Study about a FDA Approved Contact Lenses for Management of Myopia

    Official Title
    MiSight® 1 Day Post-Approval Study for Effectiveness and Visual Symptoms
    Purpose

    The purpose of this study is to evaluate if FDA approved contact lenses can reduce the progression of nearsightedness in children. Children who participate in this 4-year study will be asked to wear the study provided contact lenses at least 6 days a week and be willing to attend visits at The OSU College of Optometry one month after starting treatment and every six months thereafter. Visits will include a comprehensive eye exam and contact lens fitting at no cost.

    Could this study be right for you?
    1. Children ages 8 to 12 years old.
    2. No previous medication or contact lenses related to myopia control.
    3. Glasses and/or contact lens prescription between -0.75 and -4.00 diopters.
    4. Satisfy all other study eligibility criteria.
    Age Range
    8 - 12 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 about Treatment for Stress and Anxiety for People with Mild Cognitive Impairment and their Care Partners

    Official Title
    Treatment of Stress and Anxiety in MCI/AD: A Randomized Controlled Trial
    Purpose

    The purpose of this study is to conduct a fully powered randomized clinical trial (RCT) comparing the efficacy of interventions to reduce anxiety and related symptoms among those with Mild Cognitive Impairment or Mild Alzheimer's Disease and Related Dementias. The study also examines the efficacy of interventions to reduce care partner burden among care partners of people living with Mild Cognitive Impairment or 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