Clinical trials

77

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Virtual Reality Brief Violence Intervention: Preventing Gun Violence Among Violently Injured Adults

The overall aim of the proposed project is to develop and evaluate the effectiveness of Brief Violence Intervention-Virtual Reality (BVI-VR) for reducing firearm-related violence, re-injury, and mortality among victims of violence. Outcome measures of firearm-related violence will come from multiple sources, including criminal background checks, hospital data, state-level data, semi-structured clinical assessments, and self-report assessments. In addition, the study aims to understand the impact of BVI-VR on psychosocial mediators resulting in a reduction of firearm-related violence. This will include self-report surveys, neurocognitive assessments, and clinical assessments. The economic efficiency of BVI-VR as a firearm-related violence intervention will also evaluated. To achieve these aims, a randomized control trial (RCT) in a large sample of violently injured adults (18+ years) from VCU Health will be conducted.

Participants needed: 220
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Oct 13, 2026Locations: 1
Eligibility criteria

violently injured patients from VCU's Level 1 Trauma Center [+2]

Under 18 years old [+1]

Status: Recruiting

Does a Periaqueductal Gray-vagus Nerve Interface Malfunction Explain the Nat hx With Its Numerous Co-morbidities?

Postural tachycardia syndrome (POTS) is a common and disabling disorder among adolescents. No epidemiologic data exist to support the often cited 0.5 to 2% prevalence. Case series suggest 3 to 5 times greater incidence in girls than boys. POTS is defined in children as daily chronic symptoms of orthostatic intolerance and a 40 bpm rise in heart rate in the first 10 minutes of a tilt study in the absence of orthostatic hypotension. POTS often develops after an acute event like an illness, infection, immunization, head trauma, psychological trauma or surgery. Natural history data are absent for POTS, though some outcome studies exist. Orthostatic symptoms improve in the majority and heart rate changes improve in 38% at 1 year. A 2-year follow up showed small improvement in comorbid symptoms of POTS in a 12 subject cohort followed yearly. In a pediatric 5-year outcome follow up questionnaire study, 86% of adolescents with POTS reported resolved, improved, or intermittent, symptoms, with primarily physical rather than mental health complaints.

Participants needed: 120
Trial details
Age: 12-21Biological sex: FemaleType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

symptomatic ≥ 40 bpm rise in heart rate in the first 10 min of a tilt table stud... [+1]

Pregnant or breastfeeding [+29]

Status: Recruiting

Autonomic and Renal Contributions to Hypertension With ADT

This study plans to learn more about contributors to high blood pressure in men who undergo androgen deprivation therapy (ADT) to treat prostate cancer. Prostate cancer is the most common non-skin cancer in men, affecting approximately 1 in 8 American men and its primary treatment is through the use of ADT. However, ADT increases the likelihood of developing heart disease including high blood pressure. This study will determine if dysfunction of the nervous system and/or kidneys occurs in men undergoing ADT, as these systems play a significant role in control of blood pressure. The results from this study will help us understand the ways in which ADT contributes to heart disease and help us develop therapies to prevent heart disease in prostate cancer survivors.

Participants needed: 50
Trial details
Phase: Phase 4Age: 40+Biological sex: MaleType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 30, 2026Locations: 1
Eligibility criteria

age 40+ years; [+12]

-acute liver disease; [+6]

Status: Recruiting

Open-label Feasibility Trial of HD-tDCS During Cognitive Behavioral Therapy for Cocaine Use Disorder

Cocaine Use Disorder (CocUD) is a significant public health issue with increasing cocaine-related overdose mortality. Effective treatments for CocUD are highly needed. One understudied target for CocUD therapeutics is improving cognitive function (CF) in that key theories attribute development of CocUD and other substance use disorders (SUD) to impaired CF, such as decreased ability to inhibit behavior. Heavy cocaine users show impairments in attention, working memory, planning, and response inhibition, affecting as many as 30-80% of individuals with SUD. These cognitive deficits affect patient engagement and participation in SUD treatment, thus necessitating SUD programs assess and accommodate cognitive problems throughout treatment.

Participants needed: 36
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 28, 2026Locations: 1
Eligibility criteria

Between 18 and 65 years-of-age. [+4]

Current DSM-5 diagnosis of any non-cocaine substance use disorder (SUD) other th... [+10]

Status: Recruiting

Examining the Impact of Exercise Training on Vascular Dysfunction in Individuals With Mental Health Disorders - Study 1

The purpose of this research study is to examine the role oxidants, substances produced in the blood that can damage blood vessel function, may play in blood vessel function in healthy individuals as well as individuals with mental health disorders (posttraumatic stress disorder (PTSD) and/or generalized anxiety disorder (GAD)).

Participants needed: 720
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

apparently healthy and free of overt cardiovascular, pulmonary, or metabolic dis... [+3]

taking medications that could influence cardiovascular function [+5]

Status: Recruiting

Cardiovascular Health Education Via Virtual Reality for Breast Cancer Survivors Receiving Anthracyclines or Trastuzumab

The main goal of this study is to test a virtual reality (VR) program, Survivors' Virtual Reality Survivorship Experience (SurviVRSE), designed to help Breast Cancer survivors (n=30) learn about heart health. The aims are to test the usability, feasibility, and acceptability o the intervention. Additionally, follow-up assessments will examine changes in women's cancer therapy related cardiac dysfunction knowledge and heart healthy behaviors (e.g., physical activity).

Participants needed: 30
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 22, 2026Locations: 3
Eligibility criteria

18 years of age or older [+4]

Status: Recruiting

C-SMART vs BE Well for Patients With Brain Tumors

The goal of this clinical trial is to learn about the acceptability and feasibility of Cognitive Strategies, Mindfulness, and Rehabilitation Therapy (C-SMART) and Brain health Education and Wellness (BE Well) in adults with brain tumors and their caregivers. Participants will be assigned to one of the two groups: * Cognitive Strategies, Mindfulness, and Rehabilitation Therapy (C-SMART) is a recently developed virtual intervention combining both cognitive rehabilitation with mindfulness meditation training. The manualized program consists of 8 weekly 1:1 tele intervention sessions, targeting cognitive weaknesses identified from baseline cognitive testing. * Brain health Education and Wellness (BE Well) intervention consists of 8 weekly videos focused on maximizing brain health in the context of brain tumor. Participants will also be asked to: * participate in two in-person visits involving an MRI (if eligible for research MRIs) and neurocognitive tests * complete a survey the the beginning and end of the study * if in BE Well group, answer a few questions after watching each video

Participants needed: 56
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 25, 2026Locations: 1
Eligibility criteria

Patient of Virginia Commonwealth University Neuro-Oncology clinic [+5]

Presence of major neurocognitive impairment that would prevent participation in... [+10]

Status: Recruiting

The Role of Visual Attention and Environmental Complexity in Real-world Mobility for People With Lower Limb Amputation

Despite high medical expenses (\>$500K/patient), mobility improvements achieved during rehabilitation for people with lower limb amputation (LLA) fail to translate into improved real-world outcomes. Even with advances in prosthesis technology enabling faster gait speed, greater walking endurance, and improved mobility confidence, people with LLA report persistent dissatisfaction with real-world mobility, limited ability to walk in the community, and difficulty achieving recommended physical activity levels. Real-world walking requires thinking and moving simultaneously (e.g., cognitive-motor dual-tasking), visually attending to the environment, and navigating varying terrain. In contrast, clinical mobility assessments are usually performed without additional visual or cognitive demands, in controlled environments, and on level surfaces. Current clinical tools used to assess ambulation progression during rehabilitation do not adequately assess these changes in people who have experienced LLA.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

unilateral transtibial LLA of either dysvascular (diabetes, peripheral vascular... [+5]

congenital or cancer-related LLA [+13]

Status: Recruiting

Randomized Controlled Trial of Treatment to Optimize Heart Rate Variability for Persistent Post-Concussion Symptoms

Many combat veterans (c-Vs), service members (SMs) and civilians with mild traumatic brain injury (mTBI, also termed concussion) suffer from persistent post-concussion symptoms (PPCS) that degrade physical and cognitive well-being and have been linked with early neurodegeneration. PPCS include somatosensory (e.g., headache, disturbed vision), vestibular (e.g., dizzy, clumsy), cognitive (e.g., executive function, memory) and affective symptoms (e.g., sleep disturbance, irritability, depression). A key pathological process that provokes and perpetuates PPCS is autonomic nervous system (ANS) dysfunction such as unremitting sympathetic nervous system activation that also exacerbates other pathology such as inflammation. ANS activity can be readily quantified by measuring heart rate variability (HRV), or the variation in heart rate over time, which serves as a valid index of both physiological and psychological health

Participants needed: 148
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 22, 2026Locations: 1
Eligibility criteria

age 18 or older [+7]

Any TBI with severity greater than mild (i.e., Moderate or Severe TBI defined as... [+3]

Status: Recruiting

Metronomic Decitabine-Cedazuridine and Venetoclax in R/R AML, HR-MDS, HR/AP MPN

This is a single-center randomized phase 2 open-label clinical trial.

Participants needed: 40
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 21, 2026Locations: 1
Eligibility criteria

Age ≥18 years at time of enrollment [+10]

Prior use of hypomethylating agent and venetoclax in combination (Note, use of h... [+12]

Status: Not yet recruiting

Transcranial Doppler Evaluation After Endovascular Thrombectomy for Acute Ischemic Stroke (PRECISE-TCD)

Endovascular thrombectomy (EVT) improves outcomes in acute ischemic stroke caused by large vessel occlusion. Despite successful recanalization, early neurological deterioration (END) remains frequent and is associated with poor outcomes. Transcranial Doppler (TCD) provides noninvasive, real-time assessment of cerebral blood flow velocities and may identify hemodynamic patterns associated with deterioration after EVT. PRECISE-TCD is a prospective, single-center observational study enrolling 180-300 patients undergoing EVT for anterior circulation large vessel occlusion at a tertiary academic medical center. Serial TCD examinations are performed immediately after EVT, daily for 72 hours, and as close as possible to early neurological deterioration events or clinically indicated head CT within 72 hours. The primary outcome is the association between TCD-derived hemodynamic parameters and END within 72 hours. Secondary outcomes include NIHSS at 24 hours and discharge, discharge disposition, and modified Rankin Scale at 90 days.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Sep 14, 2026Locations: 1
Eligibility criteria

Anterior circulation large vessel occlusion, including ACA, MCA, or ICA stroke,... [+2]

Inadequate acoustic windows defined as lack of bilateral MCA signal at standard... [+2]

Status: Recruiting

Research Participation With Transgender and Gender-Diverse Youth

Research has historically excluded the participation of transgender and gender-diverse people. The purpose of this research study is to find out about what goes into a transgender and gender-diverse youth's decision to participate in research. The results of this study will be used to improve access to research for transgender and gender-diverse youth and therefore, improve the representation of transgender and gender-diverse youth as research participants in research.

Participants needed: 250
Trial details
Age: 15-21Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Sep 14, 2026Locations: 1
Eligibility criteria

Gender identity different then sex assigned at birth [+1]

Gender identity the same as their sex assigned at birth [+1]

Status: Not yet recruiting

The Impact of Improved Vagal Function on Periaqueductal Gray Connectivity

This study is being to see if participating in breathing exercise training and practicing this training will help with Postural tachycardia syndrome (POTS). The information may help doctors to learn more about how the different parts of people's brains communicate.

Participants needed: 12
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 16, 2026Locations: 1
Eligibility criteria

Age 18-50 years [+3]

Inflammatory arthritis, connective tissue or auto-immune disorder [+13]

Status: Recruiting

Integrating a Prescription Produce Program Within a Diabetes Prevention Program

Type 2 Diabetes remains a major chronic disease among adults in the United States. A way to prevent Type 2 Diabetes is to engage in a diabetes prevention program. In the diabetes prevention program, individuals at risk of Type 2 Diabetes meet with a health coach to learn effective ways to build health behaviors around diet and physical activity. Individuals who participate in the diabetes prevention program are more likely to lose weight and eat a healthy diet.

Participants needed: 96
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 9, 2026Locations: 1
Eligibility criteria

≥age 18 [+13]

Individuals with HbA1c or glucose levels above the indicated glucose ranges will... [+2]

Status: Not yet recruiting

Young Adult-Mediated Intervention to Increase Colorectal Cancer Screening

This study will garner preliminary data to develop a young adult-mediated intervention whereby a younger family member encourages their older family member to get colorectal cancer (CRC) screening. In Aim 1, survey data from n=150 younger (25-44 years old) and n=150 older (45-75 years old) adults living in rural communities will be collected. In Aim 2, intervention components will be evaluated using n=9 focus groups. The novel intervention will be assessed via a pilot trial (n=15 adult child/parent dyads) in Aim 3.

Participants needed: 30
Trial details
Age: 25-75Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 11, 2026Locations: 1
Eligibility criteria

Residents of counties in the Virginia/North Carolina CRC hotspot [+3]

Status: Recruiting

Establishing Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type 1 (END-DM1) Extension

Myotonic Dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder that causes progressive disability and shortened life expectancy. It is characterized by progressive weakness and myotonia, which preferentially affects the craniofacial, hand, and distal leg muscles. Many patients also experience difficulties with cognition, cardiac arrhythmias, respiratory failure, or cataracts. Currently there is no treatment to slow progression or reverse the symptoms.

Participants needed: 1,000
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Sep 4, 2026Locations: 1Duration: 4 Years
Eligibility criteria

Age 18 to 70 years (inclusive) [+2]

Symptomatic renal or liver disease, uncontrolled diabetes or thyroid disorder, o... [+4]

Status: Recruiting

Comparing the Attentional Demands and Functional Outcomes in People With Transradial Amputation

Different ways of controlling an upper-limb prosthesis can affect how easy it is to use and how helpful it is in everyday activities. One common method, called direct control, uses signals from two muscles and can make switching between movements difficult. Another clinically available option, called pattern recognition control, uses signals from several muscles to better understand the user's intended movement and may feel more natural to use. This study compares these two control methods to see how they affect function for adults with below-the-elbow limb loss.

Participants needed: 32
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 8, 2026Locations: 2
Eligibility criteria

18 years of age or older [+6]

Any health condition that would prevent safely completing trial activities [+1]

Status: Recruiting

FearLess in NeuroOncology

The overarching goal of this project is to assess the feasibility, acceptability, and appropriateness of recruitment methods, target population, and a waitlist design to finalize the protocol of FearLess in primary malignant brain tumor patients and caregivers

Participants needed: 112
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 9, 2026Locations: 1
Eligibility criteria

Self-report a diagnosis of a primary malignant brain tumor (grade II-IV) [+8]

Cognitive impairment that might prohibit active intervention engagement [+2]

Status: Not yet recruiting

Enhancing an Existing Prevention Strategy to Reduce Intentional Firearm Injuries Among High-risk Youth (Phase 1)

Over the past three decades, substantial resources have been devoted to developing youth violence prevention (YVP) programs. These programs have demonstrated positive effects on reducing aggression and related behaviors, firearm-specific risk factors were largely overlooked due to historical barriers to firearm research. This omission is concerning, as firearms are now the leading cause of injury and death among U.S. youth. Existing YVP strategies such as Emerging Leaders address general violence risk but do not directly target firearm-related risks or suicide prevention. There remains a critical gap in prevention strategies that integrate firearm-specific content while leveraging established program infrastructure.

Participants needed: 45
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 3, 2026Locations: 1
Eligibility criteria

Youth aged approximately 13-17 years. [+3]

Significant cognitive impairment or developmental disability that would preclude... [+1]

Status: Not yet recruiting

TENS of Auricular Vagal Nerve for Radiation Necrosis

This is a multi-center, randomized, blinded trial evaluating the effect of transcutaneous auricular vagal nerve stimulator (taVNS) on radiation necrosis-related cerebral edema. In this study, consenting and eligible patients will be assigned to one of two arms: treatment (Arm 1) or sham (Arm 2). Patients in both arms will have imaging performed and tissue and blood collected for assessment of changes in area of contrast enhancement and cerebral edema, inflammatory markers, and markers of blood-brain barrier permeability.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 4, 2026Locations: 1
Eligibility criteria

History of glioma or metastatic brain lesion previously treated with whole brain... [+4]

New onset neurologic deficits secondary to radiation necrosis requiring initiati... [+5]

Status: Not yet recruiting

Biomarker-Guided Mycophenolate Mofetil Elimination in Low-Risk Older Adult Kidney Transplant Recipients

Most kidney transplant recipients take a combination of anti-rejection medicines for the rest of their life. One of these is called mycophenolate mofetil (MMF), also known by the brand name CellCept. While MMF helps protect the kidney, taking it for many years can cause infections, low blood counts, stomach problems, and a higher risk of certain cancers, problems that older adults are especially likely to experience. We are doing this study to learn whether carefully and slowly stopping MMF in older adults who are doing well after their transplant is as safe as continuing MMF, when we use blood and urine tests to closely watch for any early signs of trouble. The information learned could help future kidney transplant patients use less medicine without losing their transplant.

Participants needed: 20
Trial details
Phase: Early Phase 1Age: 60+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 8, 2026
Eligibility criteria

Greater than 60 years of age [+4]

Multi-organ transplant or prior graft loss due to rejection [+9]

Status: Recruiting

Safety and Tolerability Study of VVZ-2471 in Healthy Volunteers

The goal of this study is to do follow-up testing on the safety and tolerability of an experimental (not FDA approved) medication. This study is seeking non-illicit drug using adults to test the medication. Results of this study will help us to develop future studies to test the medication with people who use substances. This research is supported by and included in the NIH HEAL Initiative (https://heal.nih.gov/).

Participants needed: 60
Trial details
Phase: Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 1, 2026Locations: 1
Eligibility criteria

Demographics: Male or female, between 18 and 65 years of age. [+15]

Psychosis and bipolar disorder: Any lifetime history of psychosis or bipolar dis... [+9]

Status: Not yet recruiting

Colon Health Champion Program

This is a single arm-proof-of-concept trial. The primary goal of this trial is to assess the feasibility and acceptability of the Colon Health Champion Program

Participants needed: 29
Trial details
Age: 45-75Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Sep 1, 2026Locations: 1
Eligibility criteria

Adults aged (45-75 years old) who reside in target communities. [+2]

Planning to move from the area within the study period [+11]

Status: Recruiting

Virtual Housecalls: Redesigning Pediatric Primary Care Adolescent Obesity Treatment

This pragmatic randomized clinical trial tests a novel intensive health behavior and lifestyle intervention, conducted via telehealth, to treat class I adolescent obesity in pediatric primary care. Results will inform scalable approaches that meet the recommended treatment dose and effectively treat obesity in this setting.

Participants needed: 500
Trial details
Age: 12-15Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Aug 26, 2026Locations: 1
Eligibility criteria

English or Spanish-speaking [+6]

conflicts that would inhibit the ability to participate in all aspects of the st... [+7]

Status: Recruiting

Health Education Approach to Lung Screening

Evaluate the impact of the patient navigation program on the proportion of patients who complete lung cancer screening (LCS), defined as undergoing a low dose computed tomography (LDCT)

Participants needed: 675
Trial details
Age: 50-80Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Aug 25, 2026Locations: 3
Eligibility criteria

Meets current USPSTF guidelines for lung cancer screening (LCS) [+5]

Known history of cancer (except squamous cell skin cancer), or coughing up blood... [+3]