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Search Studies

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.

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Found 197 results. Displaying page 1 of 17.
  • Research Study on the Biomechanics of Total Knee Replacements

    Official Title Biomechanical Metrics of Movement Relative to Total Knee Arthroplasty

    Purpose

    This study aims to understand how a total knee replacement surgery (TKR) affects muscle function and movement in the lower body. It focuses on four key areas:

    1. Examining how TKR changes the way muscles work in the lower body.

    2. Exploring how these muscle changes relate to the forces people experience when walking and doing daily activities after surgery.

    3. Connecting muscle function to how well patients feel and move after TKR.

    4. Identifying different types of TKR patients based on their physical traits, movement patterns, and medical history to see how they compare.

    Could this study be right for you?

    • Must be scheduled to receive a total knee replacement within the next 2 months
    • Have a body mass index (BMI) < 40
    • Do not require the use of a cane or other assistive device when walking, climbing stairs, and getting up from a chair

    Exclusion criteria varies; please contact Study Coordinator for more information

    Age Range

    18 years and up
  • Impacts of Ketone Esters on Exercise and Heart Health in Type 2 Diabetics

    Official Title Effects of Acute and Chronic Ketone Ester Consumption on Exercise Tolerance and Cardiac Function in Subjects with Diabetes

    Purpose

    This placebo-controlled study is being done to evaluate the effects of a ketone ester drink on exercise performance and heart health in a group of subjects diagnosed with type 2 diabetes.

    Could this study be right for you?

    There are additional exclusion criteria, study staff will screen fully before enrollment.

    Age Range

    18 - 80 years
  • Radiotracer Imaging of Lower Extremity Skeletal Muscle Perfusion in Patients with Peripheral Arterial Disease (PAD)

    Official Title Radiotracer Imaging of Lower Extremity Skeletal Muscle Perfusion in Patients with Peripheral Arterial Disease

    Purpose

    The purpose of this study is to look at a new method to evaluate blood flow to the calves and feet. 

    Peripheral Artery Disease (PAD) patient outcomes will be evaluated for up to 12 months after their revascularization procedure to assess how early changes in SPECT-derived foot perfusion relate to rates of diabetic wound healing and limb salvage. Outcomes will be specifically evaluated at 3, 6, 9, and 12 months after revascularization at the time of their follow-up clinic visits to the OSU Comprehensive Wound Center at OSU Hospital East. Primary outcomes of interest will be 1) changes in wound size and healing, 2) minor or major amputations of the lower extremity, and 3) any subsequent interventional procedures, such as balloon angioplasty, stenting, or surgical bypass.

     

    Could this study be right for you?

    Heathly Volunteers with out previous cardiovascular disease

    Or 

    PAD

    Age Range

    18 years and up
  • 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
  • Effect of Diet and Electrical Stimulation Exercise on Blood Pressure Control in Spinal Cord Injury

    Official Title Lifestyle solutions to postprandial hypotension in spinal cord injury

    Purpose

    To test if a low-glycemic diet and electrical stimulation of leg muscles can improve blood pressure control after eating.

    Could this study be right for you?

    • Spinal cord injury sustained at least 1-year ago
    • Level of injury between C4 and T10
    • Use of wheelchair for majority of daily activities

    Age Range

    18 years and up
  • 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
  • Does the amount of nicotine in filtered little cigars impact health and smoking habits?

    Official Title LOWFLC Study: Addiction potential of low nicotine filtered little cigars

    Purpose

    Researchers from The Ohio State University are recruiting adult users of little cigars and cigarillos to help improve understanding of the products’ health impact.

    Could this study be right for you?

    • Current smoker
    • No significant health problems

    Age Range

    21 - 75 years
  • A Study for Reducing Alcohol Use During MOUD (Phase Two)

    Official Title Brief Digitally Enhanced Intervention for Managing Emotional Pain and Reducing Alcohol Use during Medication for OUD (Phase Two)

    Purpose

    This study is being done to further examine and improve how a brief clinical treatment intervention may reduce alcohol use among patients engaged in medication for opioid use disorder (MOUD) treatment.

    The length of the study is approximately 10 weeks and will include two on-campus lab visits at Ohio State's Medical Campus, daily surveys via a smartphone app (surveys 3 times a day for ~21 days), three treatment sessions (completed online or in-person), and follow-up questionnaires (completed online). The total time commitment of the study is 11 hours and 6 minutes.

    Could this study be right for you?

    Inclusion Criteria:

    • engaged in MOUD treatment (for at least one month)
    • alcohol consumption (within the past 12 months)
    • age 18 or older
    • access to a smart phone

    (partial list of inclusion criteria)

    Exclusion Criteria:

    • diagnosis of psychosis or bipolar I
    • currently pregnant (positive pregnancy test)

    (partial list of exclusion criteria)

    Age Range

    18 years and up
  • A Study for Reducing Alcohol Use During MOUD (Phase One)

    Official Title Brief Digitally Enhanced Intervention for Managing Emotional Pain and Reducing Alcohol Use during Medication for OUD (Phase One)

    Purpose

    This study is being done to adapt and improve a brief clinical treatment intervention that aims to reduce alcohol use among patients engaged in medication for opioid use disorder (MOUD) treatment.

    The length of the study is approximately 4 weeks and will include an initial study visit, daily surveys via a smartphone app (surveys 5 times a day for ~21 days), and three treatment sessions. All study sessions can be completed online or in-person. The total time commitment of the study is 8 hours and 30 minutes.

    Could this study be right for you?

    Inclusion Criteria:

    • engaged in MOUD treatment (for at least one month)
    • alcohol consumption (within the past 12 months)
    • age 18 or older
    • access to a smart phone

    (partial list of inclusion criteria)

    Age Range

    18 years and up
  • Evaluating the Safety and Usefulness of an Investigational Study Drug for Treating Patients with Bipolar Depression

    Official Title Depressive Episodes Associated with Bipolar I or II Disorder: A Double-Blind,
    Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of
    ABBV-932

    Purpose

    The purpose of this study is to see if the investigational study drug is safe and useful for treating patients with bipolar depression.

    Eligible participants will be randomized to receive the drug or placebo. A placebo looks just like the investigational study drug but has no active drug in it.

    The maximum duration of the study treatment period is 6 weeks. Participants receive psychiatric evaluation at each visit, and physical exam, urine test and blood draws at some of the visits. All study medication and procedures are provided at no cost, and participants may be compensated for their time and travel for each visit attended.

    Could this study be right for you?

    A diagnosis of bipolar disorder (type I or II) and be currently depressed.

    Age Range

    18 - 65 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
  • Psilocybin Study for Treatment - Resistant Depression

    Official Title A Phase III, multicentre, randomised, double-blind,
    controlled study to investigate the efficacy, safety,
    and tolerability of two initial administrations of
    COMP360 in participants with treatment-resistant
    depression

    Purpose

    The study investigates a new approach for treatment-resistant depression using an investigational medicine related to psilocybin alongside psychological support.

    Could this study be right for you?

    You may be able to join the study if you:

    —         Are 18 years of age or older

    —         Have been diagnosed with major depression and have not responded to 2+ antidepressants

    Other criteria will need to be met to confirm your eligibility for this study, which will last up to 62 weeks.

    Age Range

    18 years and up