• Long-term Follow-up of Adults Who Experience an out of Hospital Cardiac Arrest

    Official Title Patterns Of Survivors’ Recovery Trajectories in the ICECAP trial 􀂥POST-ICECAP􀂦

    Purpose

    The purpose of this study is to describe the physical, neuropsychological outcomes of adults who have experienced an outside of hospital cardiac arrest; and examine any associations between those outcomes and any clinical and/or rehabilitative interventions and/or social determinants of health.

    Could this study be right for you?

    • Experienced a coma after resuscitation from a cardiac arrest
    • Received targeted/controlled body temperature management
    • Survived to at least 1 month after experiencing a outside of hospital cardiac arrest

    Age Range

    18 years and up

    Contact Information

    The Ohio State University Medical Center Emergency Department- Main and East
    Carson Reider, PhD
    614-366-5431
  • Healthy Diet Study

    Official Title A prospective randomized unblinded study of ketogenetic versus mixed diet on exercise tolerance in subjects with the metabolic phenotype of heart failure with preserved ejection fraction

    Purpose

    The purpose of this study is to compare the effects of a well-formulated ketogenic diet with a low-fat diet on exercise tolerance in patients with diabetes or pre-diabetes or obesity; with shortness of breath or heart failure.

    Could this study be right for you?

    Inclusions:

    • Age ≥ 18 years old and ≤ 80 years old & willingness to be randomized to either diet.
    • NYHA class I – III for at least 3 months.
    • Ejection fraction ≥40% by biplane 2D, or 3D echo, or CMR.
    • Echo findings of abnormal or indeterminant diastolic function or RHC data: At rest: mean pulmonary capillary wedge pressure (PCWP) > 15 mmHg. Pulmonary vascular resistance (PVR) < 3 Wood Units.
    • Stable medical therapy for at least 3 months as determined by the treating physician (no new cardiac or diabetic medications within 3 months of enrollment or during enrollment and dosage should be stable for 1 month prior to enrollment).
    • Dose of oral diuretics changes allowed but must be stable for 1 week prior to randomization.
    • Body Mass Index (BMI) ≥ 25 and ≤ 50 or Type 2 Diabetes Mellitus or prediabetes (fasting glucose of 100 - 125 mg/dL or hemoglobin A1C 5.7-6.4%) or metabolic syndrome.
    • Ability to participate in exercise treadmill testing.
    • Ability to sign written consent.

    Exclusions:

    • Women who are pregnant, current breast-feeding, or have intention to become pregnant while in the study.
    • Known allergy or sensitivity to gadolinium-based contrast agents.
    • Implanted pacemaker, cardioverter defibrillator, Cardiac resynchronization therapy, left ventricular assist devices.
    • Other metallic implants/aneurysm clips that are contraindicated in MRI.
    • Claustrophobia
    • History of severe kidney disease of eGFR < 30 ml/kg/1.73m2.

    Exclusion Criteria varies, please contact Study Coordinator.

    Age Range

    18 - 80 years

    Contact Information

    The Ohio State University
    Debbie Scandling
  • PREVENTABLE

    Official Title PRagmatic EValuation of evENTs And Benefits of Lipid-lowering in oldEr adults

    Purpose

    The purpose of PREVENTABLE is to learn if taking a statin could help older adults live well for longer by preventing dementia, disability, or heart disease. The duration of the study will last 5 years. 

    Could this study be right for you?

    Inclusion Criteria:

    • Community-dwelling adults
    • Age ≥75 years
    • English or Spanish as primary language

     

    Exclusion Criteria:

    • Clinically evident cardiovascular disease defined as prior myocardial Infarction (MI), prior stroke, prior revascularization procedure, or a secondary prevention indication for a statin (clinician determined)
    • Hospitalization for a primary diagnosis of heart failure in the prior 12 months (Note: History of heart failure in the absence of recent hospitalization or clinically evident cardiovascular disease is not an exclusion)
    • Dementia (clinically evident or previously diagnosed)
    • Dependence in any Katz Basic Activities of Daily Living [ADL] (with the exception of urinary or bowel continence)
    • Severe hearing impairment (preventing phone follow up)
    • Unable to talk (preventing phone follow up)

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

    Age Range

    75 years and up

    Contact Information

    Rece Foss
    614-685-3089
  • 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

    Contact Information

    Stacey Park
    614-292-3300
  • Evaluating a Mobile Health App for Cardio-Oncology Patients

    Official Title Mobile Health App as a Cardiotoxicity Symptom Logging Tool: Feasibility Pilot Study

    Purpose

    To evaluate the cardio-oncology patient population’s experience with using smart-phone technology as a part of self-management with their care through features such as symptom logging and education. Eligible patients will be asked to participate in a 30-minute virtual interview and/or a 60-minute virtual design or usability session to discuss their thoughts on a mobile app for cardio-oncology patients.

    Could this study be right for you?

    • English-speaking
    • Prior cancer diagnosis
    • Currently undergoing a cancer regimen that includes a targeted, biologic, radiation, and/or immune-based therapy (e.g., TKIs and/or ICIs).
    • No pregnant females
    • No prisoners

    Age Range

    18 and up

    Contact Information