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Research institution

Indiana University Clinical Trials

Studies where Indiana University is the lead sponsor: what is enrolling now, by phase, condition and country.

1,077 registered studies

In numbers

Open to volunteers
196
Active
221
With results posted
337
All registered
1,077

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 196
  • Pregnancy Preterm, Premature Birth

    The Periviable GOALS Decision Support Tool

    • Recruiting
    • Age: 18 years and older

    The Periviable GOALS (Getting Optimal Alignment around Life Support) decision support tool (DST) is meant to facilitate informed shared decision-making regarding neonatal resuscitation for families facing the threat of a…

    Conditions
    Pregnancy Preterm, Premature Birth, Pregnancy Complications, Obstetric Labor, Premature
    Trial name
    NCT05264779
    Testing
    Periviable GOALS DST
    Where
    12 sites in United States
    Volunteers
    300 people
    Sponsor
    Indiana University
    Can I take part? NCT05264779
  • Testicular Cancer, Survivorship

    Late Subclinical Cardiovascular Disease in Testicular Cancer Survivors

    • Recruiting
    • Age: 18 to 99 years
    • Observational study

    Late subclinical cardiovascular disease in testicular cancer survivors exposed to cisplatin-based chemotherapy and bone marrow transplant

    Conditions
    Testicular Cancer, Survivorship, ASCVD, Coronary Artery Disease
    Trial name
    NCT05611307
    Testing
    Lipid profile, Coronary artery assessment, Hormone levels for hypogonadism
    Where
    United States
    Volunteers
    150 people
    Sponsor
    Indiana University
    Can I take part? NCT05611307
  • Binge Eating, Overweight and Obesity

    Cognitive and Behavioral Approaches to Reduce Binge Eating and Excess Weight in Adolescents (Online)

    • Not yet recruiting
    • Age: 12 to 17 years
    • Lifestyle or therapy programme

    This study will compare a psychological treatment (cognitive-behavioral therapy; CBT-BED) and a lifestyle beahvioral obesity intervention (LBOI) for adolescents who experience binge eating and have overweight or obesity.

    Conditions
    Binge Eating, Overweight and Obesity, Eating Disorders in Adolescence
    Trial name
    CARE2 (NCT07856784)
    Testing
    Cognitive-Behavioral Therapy for Adolescent Binge Eating, Lifestyle Behavioral Obesity Intervention, Active Control
    Where
    United States
    Volunteers
    159 people
    Sponsor
    Indiana University
    Can I take part? CARE2
  • Plasma Cell Dyscrasias

    The Indiana Myeloma Registry

    • Recruiting
    • Age: 18 years and older
    • Observational study

    This is a prospective, non-interventional, observational study. The purpose of this study is to collect data and bio-specimens that will support future research

    Trial name
    NCT03616483
    Testing
    This is a non-interventional trial
    Where
    United States
    Volunteers
    2,500 people
    Sponsor
    Indiana University
    Can I take part? NCT03616483
  • Alcohol Use, Adolescent

    Evaluating Caregiver Involvement in Primary Care-Based Brief Interventions for Adolescent Alcohol Use Problems

    • Recruiting
    • Age: 12 to 18 years
    • Lifestyle or therapy programme

    Intervention for mild severity alcohol use among U.S. teens is crucial, as alcohol is the most commonly used substance in this age group, yet few receive the necessary interventions.

    Conditions
    Alcohol Use, Adolescent, Mild Alcohol Use Disorder, Mild Substance Use Disorder
    Trial name
    NCT06593652
    Testing
    Teen Intervene - Adolescent Only, Teen Intervene with Caregiver Session, Family Check Up
    Where
    United States
    Volunteers
    615 people
    Sponsor
    Indiana University
    Can I take part? NCT06593652
  • Depression, Treatment Resistant

    rTMS to Target Neural Connectivity and Rumination in Treatment-Resistant Depression

    • Recruiting
    • Age: 18 to 70 years
    • Medical device

    The goal of this clinical trial is to learn if Transcranial Magnetic Stimulation (TMS) to part of the brain called the ventromedial prefrontal cortex (VMPFC) can treat a symptom called rumination in adults with major depression…

    Trial name
    NCT06511544
    Testing
    Transcranial magnetic stimulation
    Where
    United States
    Volunteers
    20 people
    Sponsor
    Indiana University
    Can I take part? NCT06511544
  • Heart Failure With Preserved Ejection Fraction

    Leg Heat Therapy in Heart Failure With Preserved Ejection Fraction

    • Recruiting
    • Age: 18 years and older
    • Medical device

    The objective of this pilot study is to establish evidence to support the validity of HT in improving skeletal muscle function and physical capacity of patients with HFpEF.

    Trial name
    NCT06388226
    Testing
    Leg heat therapy
    Where
    2 sites in United States
    Volunteers
    90 people
    Sponsor
    Indiana University
    Can I take part? NCT06388226
  • Acute Kidney Injury, Fluid Overload

    Assessment of Worldwide Acute Kidney Injury Epidemiology in Neonates 2.0

    • Enrolling by invitation
    • Age: 0 minutes to 2 weeks
    • Observational study

    There is a growing focus on short- and long-term kidney health in neonates, including those with acute kidney injury (AKI). AKI occurs commonly in the Neonatal Intensive Care Unit (NICU) and is associated with adverse outcomes.

    Conditions
    Acute Kidney Injury, Fluid Overload, Prematurity Complications, Risk Factors
    Trial name
    AWAKEN 2 (NCT06823115)
    Where
    125 sites in United States, Argentina and 31 more
    Volunteers
    8,000 people
    Sponsor
    Indiana University
    Can I take part? AWAKEN 2
  • Pregnancy

    Impact of Standardization on Outcomes Following Cervical Ripening

    • Recruiting
    • Age: 18 years and older
    • Phase 2/3
    • Medical device

    The primary purpose of this study is to determine if vaginal delivery rate is impacted by the use of standardized methods of cervical ripening. Additional outcomes will be evaluated including maternal and fetal outcomes of labor.

    Trial name
    NCT07576881
    Testing
    Cervical Ripening with a double balloon catheter only, Cervical ripening with a double balloon catheter plus misoprostol, Usual-care control group
    Where
    United States
    Volunteers
    1,158 people, healthy volunteers welcome
    Sponsor
    Indiana University
    Can I take part? NCT07576881
  • Alzheimer Dementia (AD), Caregiver Burden of People With Dementia

    VICA: A Virtual Care Assistant for Dementia Caregivers

    • Not yet recruiting
    • Age: 21 years and older
    • Medical device

    This pilot randomized controlled trial evaluates the feasibility and preliminary efficacy of VICA, an AI-powered virtual care assistant that delivers evidence-based education, symptom monitoring, and coaching to informal…

    Trial name
    VICA (NCT07779785)
    Testing
    VICA - Virtual Informal Care Assistant, Education only BPSD mobile app
    Where
    United States
    Volunteers
    120 people
    Sponsor
    Indiana University
    Can I take part? VICA

Completed, with results posted

All 264
  • Acute Lymphoblastic Leukemia, Pediatric, Pediatric Cancer

    Biology and Benefits of Music Play and Stories for Kids/Parents During ALL Treatment

    • Completed
    • Age: 3 to 8 years
    • Lifestyle or therapy programme
    • Results posted

    Music therapy has become a standard palliative care service in many pediatric and adult hospitals; however, a majority of music therapy research has focused on the use of music to improve psychosocial dimensions of health…

    Trial name
    NCT04400071
    Testing
    Active Music Engagement, Audio Storybooks
    Where
    4 sites in United States
    Volunteers
    192 people
    Sponsor
    Indiana University
    Can I take part? NCT04400071
  • Healthy Volunteers

    Temporal Interference Methods for Non-invasive Deep Brain Stimulation, Study 1.2

    • Completed
    • Age: 18 to 50 years
    • Medical device
    • Results posted

    In its totality, this grant aims to develop a line of research using temporal interference (TI) electrical neurostimulation technology to understand the causal role of deep brain structures in cognition.

    Trial name
    NCT07339072
    Testing
    Temporal Interference (TI) Electrical Stimulation - NAcc 5 Hz TI Active, Temporal Interference (TI) Electrical Stimulation - NAcc 10 Hz TI Active
    Where
    United States
    Volunteers
    30 people, healthy volunteers welcome
    Sponsor
    Indiana University
    Can I take part? NCT07339072
  • Vagus Nerve Stimulation

    Recording Cutaneous Vagal Nerve Activity With Multi-Electrode Array (MEA) in Patients Undergoing VNS Therapy

    • Completed
    • Age: 18 to 80 years
    • Medical device
    • Results posted

    The overall purpose of the ABVN Phase 2 grant is to expand on previous work evaluating vagal nerve function. This will be accomplished through several independent, but related, studies.

    Trial name
    NCT06827548
    Testing
    Multi-Electrode Array (MEA) Recording
    Where
    United States
    Volunteers
    22 people
    Sponsor
    Indiana University
    Can I take part? NCT06827548
  • CBD, Transplant Complication

    Drug-gene-nutraceutical Interactions of Cannabidiol and Tacrolimus

    • Completed
    • Age: 18 to 75 years
    • Phase 1
    • Results posted

    The information learned in these studies will help to inform doctors as to how to appropriately adjust doses of cannabidiol and tacrolimus in order to improve health outcomes and long-term treatment success for transplant…

    Conditions
    CBD, Transplant Complication, Kidney Disease, Chronic
    Trial name
    NCT05490511
    Testing
    Tacrolimus single dose, Epidiolex single dose, Epidiolex steady-state and tacrolimus single dose
    Where
    United States
    Volunteers
    57 people, healthy volunteers welcome
    Sponsor
    Indiana University
    Can I take part? NCT05490511
  • Dementia, Alzheimer Disease

    Aging Brain Care Virtual Program

    • Completed
    • Age: 18 years and older
    • Lifestyle or therapy programme
    • Results posted

    The program involves a virtual intervention to be delivered by RN or SW care coordinators over one year. Every care partner will receive monthly virtual visits during the first 3 months and then quarterly or more depending on…

    Trial name
    ABCV (NCT06245499)
    Testing
    Aging Brain Care Virtual Program
    Where
    United States
    Volunteers
    987 people
    Sponsor
    Indiana University
    Can I take part? ABCV

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