• Seat Belt Comfort Study

    Official Title Variation in Thoracic and Abdominal Shapes and their Influence on Posture and Seat Belt Fit for Adolescent Females

    Purpose

    We aim to understand how torso shape and bra design influence good vs. poor seat belt fit, posture, and comfort in cars.

    Could this study be right for you?

    To participate, you must be female, between 10–21 years old, in good health, a current bra-wearer, and willing to attend one 3-hour appointment at the OSU campus in Graves Hall (333 W. 10th Ave, Columbus, OH, 43210).

    Age Range

    10 - 21 years
  • Making Colorectal Cancer Screening Simple and Accessible Through Technology

    Official Title Digital Transformation of CRC Screening: Revolutionizing Access and Saving Lives

    Purpose

    The purpose of this study is to conduct usability testing to evaluate ease of use and overall user experience of a website designed to promote colorectal (CRC) awareness and screening uptake among adults 45-64.

    Could this study be right for you?

    Inclusion Criteria: Eligible participants will 1) be between the ages of 45-64, 2) at average risk for CRC and 3) from diverse racial/ethnic and socioeconomic backgrounds 

     

    Those who are ineligible fall under the following categories:  

    1. Age: Individuals outside the age range of 45-64 will be excluded

    2. Pregnancy Status: Pregnant individuals will be excluded from the study. since CRC screening is not recommended for pregnant individuals

    Age Range

    45 - 64 years
  • Postpartum Depression Study

    Official Title A Multicenter, Randomized, Double-Blind, Parallel-Group
    Dose-Controlled Study Evaluating the Safety and Efficacy of
    RE104 for Injection in the Treatment of Patients with
    Postpartum Depression (PPD)

    Purpose

    The purpose of this study is to compare the effectiveness of two doses of an experimental medication, administered once, in reducing symptoms of depression in patients with postpartum depression.

     

    Eligible participants will be assigned by chance to one of the two doses of the medication. The study includes 6 in-person visits and 4 telephone calls for up to 8 weeks.

    Could this study be right for you?

    To be eligible for this study, participants must meet the following criteria:

    • Female aged 18 to 45 years
    • Less than 12 months since delivery
    • Currently depressed
    • Not currently breastfeeding

    Age Range

    18 - 45 years
  • MOMI Study

    Official Title The mom and infant outcomes (MOMI) study: A trial of perinatal outpatient delivery systems

    Purpose

    ​To improve our ability to provide the best possible care to every mom and infant, we are testing two different models of primary care during the first year after childbirth.

    Could this study be right for you?

    • You may qualify if you’re currently pregnant – AND – you’ve ever had high blood pressure, diabetes, depression, or anxiety, including during pregnancy.

    If you participate, you’ll be randomly assigned to an Ohio State location that delivers one of two models of care. Providers at all locations can help you manage your health, but the models differ in several ways.

    • You’ll complete three study visits with surveys, several measurements, and blood and hair sampling. We’ll collect cord blood and review medical records.
  • PROMISE

    Official Title PRenatal and Obstetric Maternal Exposures and ISlet Autoantibodies in Early Life (PROMISE)

    Purpose

    The purpose of this study is to find out more about how health and exposures during pregnancy, such as having an infection, diet and growth may impact later risk of islet autoimmunity in the
    child. We are also interested in finding out more about why having a father or sibling with type 1 diabetes increases risk of autoimmunity in the child than having a mother with type 1 diabetes.

    Could this study be right for you?

    Inclusion:

    • Pregnant women:
      • who is between 8-24 weeks gestation with a singleton pregnancy
      • have had type 1 diabetes for at least 12 months, or the father of the baby or a full sibling of the baby has type 1 diabetes
      • is 18 years of age or older
      • is willing to have blood collected and to complete questionnaires about prenatal exposures once per trimester during their pregnancy (up to 3 visits) and up to 12 weeks after they deliver their baby
      • is willing to have their baby screened for genetic risk for type 1 diabetes, to complete online questionnaires, and to have their child followed for measurement of islet autoimmunity according to the determined risk for type 1 diabetes, through 5-7 years of age.
        • If low risk, two screenings: the first at 2 years of age and the second between 5-7 years of age
        • If high risk, five screenings: every six months through 2 years of age, and one between 5-7 years of age

    The father of the baby will also be asked to complete one visit during pregnancy but it is not mandatory.

    Exclusion:

    • Multiple Gestation pregnancy
    • Mother unable to consent due to intellectual impairment
    • Fetus with known medical issue that would affect study participation
    • Surrogate / gestational mothers who are not biologically related to offspring they are carrying

    Age Range

    18 years and up
  • Breathing Training Program for Breast Cancer Survivors with Obesity

    Official Title Reducing exercise intolerance through inspiratory muscle training in obese breast cancer survivors (IMOCS)

    Purpose

    The purpose of this study is to better understand why some survivors of breast cancer have difficulty exercising. We also want to learn if breathing exercises can make it easier to tolerate exercise. 

    Could this study be right for you?

    • Breast Cancer Survivor
    • Completed treatment within 6 months–5 years
    • Have obesity, defined as body mass index between 30-50 kg/m2
    • Can exercise independently

    Age Range

    18 years and up
  • 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
  • Treatment of Chronic Hepatitis C Virus During Pregnancy

    Official Title Safety, Tolerability, and Outcomes of Velpatasvir/SofosbuviR in Treatment of Chronic Hepatitis C Virus during Pregnancy (STORC), pregnant woman

    Purpose

    This study involves evaluating a medication for hepatitis C in pregnant women. 

    If you are a pregnant woman with chronic hepatitis C and you join the study, you are consenting to enroll yourself and your baby after he/she is born.

    Maternal participants will have 7 visits over approximately 7 months. Infant participants have four visits over approximately the first year of life.

    Could this study be right for you?

    (This is not a complete list)  

    • Must be 18 - 45 years of age
    • Chronic HCV infection of at least 6 months
    • Singleton pregnancy at 20 + 0 to 30 + 0 weeks’ gestation
    • Documented negative Hepatitis B testing for current infection (negative HBsAg test) prior to enrollment
    • If living with HIV, must be on antiretroviral therapy

    Exclusion Criteria (not a complete list)

    • Plans to relocate away from the study site area in the next 16 months and unable/unwilling to return for study visits
    • History of cirrhosis
    • Known fetal chromosomal abnormality prior to enrollment

    Age Range

    18 - 45
  • Assessing Responses to Exercise in the Heat in Trained Women

    Official Title Assessing Responses to Exercise in the Heat in Trained Women

    Purpose

    The purpose of this research study is to conduct exercise in hot and neutral environments on women who are aerobically trained and resistance trained to characterize and compare responses across physiologic, perceptual, and neurocognitive domains. Our rationale for this investigation is that its completion would provide evidence as to how women of different fitness backgrounds respond to exercise in the heat and how that response is different from exercising in thermoneutral conditions to better describe how the female body tolerates exercise in the heat with implications for those in recreation, competitive sports, and occupation that expands to emergency and military services.

    Could this study be right for you?

    • Aerobically Trained: having a measured aerobic capacity in the 80th percentile according to age

    • Resistance Trained: able to squat 120% and bench press 60% of their body weight.

    • Unacclimatized: participants had not been consistently exposed to hot conditions (i.e., sauna, hot yoga, etc.) in the past 2 months.

    Age Range

    18 - 35
  • Young Women’s Health Study

    Official Title An Intervention Study about Primary Care Algorithms for Early Identification of Young Women with von Willebrand Disease

    Purpose

    Researchers at Nationwide Children’s Hospital are seeking volunteers to be a part of a study looking at how to best screen for bleeding disorders in young women.

    Participants will be asked to undergo a finger prick blood test and complete questionnaires. If their survey answers suggest they have heavy menses or abnormal bleeding, they will also be asked to have a blood draw on the same day.

    Could this study be right for you?

    • Are 9 to 21 years old
    • Have had your first menstrual cycle

    Age Range

    9 - 21