Clinical trials

20

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

Condition / disease
Location
Status: Recruiting

Disentangling the Effects of Daily Stress, Sleep, and Sex Hormones on Accelerated Vascular Aging in Midlife Women

The purpose of this study is to identify the impact of estradiol (E2) on the associations between (a) responsivity to daily stress or (b) sleep variability with vascular function in midlife premenopausal women.

Participants needed: 30
Trial details
Phase: Phase 4Age: 40-55Biological sex: FemaleType: InterventionalSponsor: University of DelawareUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

Female [+2]

Pregnancy (including a positive urine pregnancy test), planning to become pregna... [+14]

Status: Recruiting

Category Learning Retention in Adults With and Without Developmental Language Disorder

Approximately 7% of the population experiences developmental language disorder (DLD), a language disorder with unclear causes. DLD affects communication beyond adolescence and poses challenges for education and career advancement due to difficulties in learning and memory. Recent research suggests that adults with DLD struggle with overnight memory consolidation, indicating a need for effective learning and memory support. This project aims to determine the optimal training schedule for perceptual memory retention in adults with and without DLD. The study involves recruiting 240 adults (120 with DLD, 120 without) for speech-perceptual training with different training schedules. The researchers predict that the manipulation of training schedules will interact with circadian preference and overnight consolidation, leading to the discovery of the best practice schedule for speech sound retention. Additionally, 300 more adults (150 with DLD, 150 without) will be recruited to investigate how optimal training schedules interact with reflexive and reflective learning strategies. The time course of learning and retention will be tracked during reflexive and reflective categorization training in six different training schedules.

Participants needed: 540
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: May 29, 2026Locations: 2
Eligibility criteria

native speakers of American English [+5]

History of neurological disorders [+3]

Status: Recruiting

Exercise and Motor Learning After Stroke (Study #3)

Subjects with chronic stroke (\> 6 months post-stroke) will learn a new walking pattern through distorted visual feedback. Retention of the pattern will be tested without visual feedback immediately after learning and 24 hours later. Subjects will be randomly assigned to the control group or the exercise group. The control group will simply complete the learning task. The exercise group will complete 5 minutes of exercise immediately following the first retention test to test for the effects of exercise on retention 24 hours later.

Participants needed: 80
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: May 20, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Menopausal Hormones and Sympathetic Activation

The purpose of this study is to understand how changes in menopausal hormones like estradiol and follicle-stimulating hormone (FSH) impact sympathetic nervous system function. To do so, the investigators will use a medication to control the production of estradiol and FSH, and in some participants, add-back estradiol to isolate its effects. The investigators will measure sympathetic activation centrally (in the brain using MRI), peripherally in the nervous system, and also examine adrenergic receptor mediated control of vascular function.

Participants needed: 80
Trial details
Phase: Phase 4Age: 40-58Biological sex: FemaleType: InterventionalSponsor: University of DelawareUpdated: Mar 27, 2026
Eligibility criteria

Perimenopausal (based on changes in menstrual cycle) [+1]

History of CVD, blood clots, stroke [+11]

Status: Recruiting

Forebrain Electroneutral Transporters in Salt-sensitive Hypertension: an MRI Study

The overall objective of this project is to identify the key salt-sensing regions of the brain and determine the underlying mechanism of sodium sensing. The investigators will assess how the brain responds to an acute increase of salt in the blood using MRI. This will be done during a 30-minute infusion of a saline solution containing 3% salt. One trial will be conducted with a salt sensing channel blocker and one trial without the salt sensing channel blocker. This will help to assess the role of a specific salt sensing channel in the brain. Salt sensitivity of BP will be assessed using 7-day dietary feeding where participants will be given food to consume for 7-days. Comparisons will be made between salt resistant (no change in blood pressure going from low to high salt diets) and salt sensitive adults (a change in blood pressure going from low to high salt diets). The investigators think the changes in MRI will be greater in salt sensitive compared to salt resistant subjects.

Participants needed: 120
Trial details
Phase: Phase 4Age: 40-60Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Mar 24, 2026Locations: 1
Eligibility criteria

Age: > 40 years or < 60 years [+4]

Age: < 40 years or > 60 years [+16]

Status: Recruiting

Mechanisms Underlying the Protective Vascular Effects of Dietary Potassium in Humans

Americans continue to consume high amounts of sodium. Potassium is notable for its blood pressure lowering effects but less is known regarding its effect on the vasculature. This investigation seeks to determine the role of dietary potassium on the vasculature in the presence of a high sodium diet in salt-resistant adults.

Participants needed: 90
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

healthy [+2]

hypertension [+10]

Status: Recruiting

Nested Pilot Study Comparing Two Treatments to Reduce Type 2 Diabetes Risk in At-Risk Delawareans

This nested pilot Randomized Clinical Trial will determine whether the Diabetes Prevention Program (DPP) enhanced with evidence-based sleep health and time restricted eating interventions ("DPP++") is more effective than the DPP alone for improving metabolic and cardiovascular metrics in 40 overweight/obese adults with prediabetes.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older [+2]

Age younger than 18 years [+5]

Status: Recruiting

Pain and Split-belt Motor Learning in Older Adults

The purpose of this research is to investigate the impact of acute pain, induced using an experimental pain paradigm of capsaicin paired with heat, on implicit locomotor learning and its retention in older adults.

Participants needed: 34
Trial details
Age: 55-90Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Dec 4, 2025Locations: 1
Eligibility criteria

Age 55-90 years old [+4]

Resting heart rate < 50 or > 100 bpm [+16]

Status: Recruiting

Online Interplay Between Deciding and Acting With Mild Cognitive Impairment

The investigators aim to understand the interplay and neural structures involved with decision--making and movement for participants with mild cognitive impairment. Rapidly deciding and acting becomes bottlenecked with mild cognitive impairment and Alzheimer's, leading to detrimental outcomes such as falling and car crashes. The investigators work will have a tangible impact by discovering sensitive biomarkers to detect disease onset and pave the way for informed and effective neurorehabilitation.

Participants needed: 60
Trial details
Age: 45-90Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Oct 15, 2025Locations: 1
Eligibility criteria

age 45 - 90 years [+4]

Any injury or condition that impacts reaching [+4]

Status: Recruiting

Linking Affective Dynamics in Response to Daily Stress to Peripheral Vascular Function in Working Age Adults

The objective of this proposal is to determine whether heightened negative affective responsivity (NA-R) to daily stressors is related to blunted nitric oxide (NO)-mediated endothelium-dependent dilation (EDD) in working age adults and the extent to which this association is impacted by major depressive disorder (MDD).

Participants needed: 18
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Sep 17, 2025Locations: 1
Eligibility criteria

Males and females aged 18-55 yrs [+4]

<18 or >55 yrs [+8]

Status: Recruiting

Examining the Feasibility of Implementing a Hypertension Storytelling Intervention Among African Americans

The purpose of this study is to assess if storytelling is an effective approach for promoting lifestyle and behavioral change among individuals managing hypertension and to determine if storytelling interventions can help to reduce blood pressure and improve medication adherence.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Jul 17, 2025Locations: 1
Eligibility criteria

African American/Black [+2]

Cognitive limitations that limit the ability to provide informed consent [+3]

Status: Recruiting

Disclosure Intervention for People in Treatment for Opioid Use Disorder

The goal of this clinical trial is to test a disclosure intervention among people in treatment for opioid use disorder. The main question it aims to answer is whether people who receive a disclosure intervention have better treatment- and recovery-related outcomes one year after receiving the intervention. Participants will complete a brief disclosure intervention designed to help them (1) make key disclosures related to disclosure and (2) build skills to disclose. Researchers will compare results to participants in a waitlist comparator condition, who receive the intervention at the end of the study.

Participants needed: 480
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Jul 18, 2025Locations: 1
Eligibility criteria

Client of Brandywine Counseling & Community Services [+2]

Diagnosis of schizophrenia [+1]

Status: Recruiting

Vascular Function and Oxidative Stress in Emergency Medical Responders

The goal of this clinical trial is to characterize blood vessel function and oxidative stress (a harmful condition that damages cells and tissues) in emergency medical technicians (EMTs). The main questions it aims to answer are: 1. Does an overnight shift work in emergency medical technicians reduce blood vessel function and increase oxidative stress? 2. Can supplementing with antioxidants help reduce the negative effects of night shift work in emergency medical technicians? Researchers will compare antioxidants to a placebo (a look-alike substance that contains no drug) to see if antioxidants work in reducing the negative effects of night shift work in emergency medical technicians. Participants will: 1\. Report to the lab two separate times following an overnight shift to assess blood vessel functioning and oxidative stress 3. Take an antioxidant supplement or placebo during each night of shift work.

Participants needed: 45
Trial details
Age: 20-40Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: May 22, 2025Locations: 1
Eligibility criteria

Body mass index between 18.5 and <35 kg/m² [+4]

Participant is unwilling or unable to give consent [+7]

Status: Not yet recruiting

Validation of Texture Changing Coatings for Use in At-Home Rapid Tests

At-home testing is an important part of mitigating the spread of COVID-19, but these tests are not accessible to people with low vision or blindness. Instead of adapting to a technology originally built for sighted people, investigators propose a no-power version that reports test results through a texture change, which people can feel by touch. This platform could be used not only for COVID, but also for other diagnostics, and will promote the independence and privacy for people with low vision or blindness by removing the need for human assistance or an internet connection.

Participants needed: 20
Trial details
Age: 12+Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Apr 6, 2025Locations: 1
Eligibility criteria

Visual Impairment: Participants should be blind or visually impaired for greater... [+2]

Limb Conditions: Participants with amputations or outer extremity conditions aff...

Status: Recruiting

Light Therapy Intervention in Individuals With Parkinson's Disease

The study looks to investigate the effects that light therapy delivered to the frontal cortex could have on Parkinson's disease related symptoms ( both cognitive and motor). The therapy is a non invasive technique that deliverers low level wavelength light to the front part of the head for 12 minutes. for this study the therapy will be done 3 times a week for 6 weeks. To measure the potential effects on the therapy in Parkinson symptoms, we will do a set of cognitive and motor test before and after the intervention to measure any changes as well as control for any potential markers such as age, sex, disease level, medication and exercise.

Participants needed: 20
Trial details
Age: 50-80Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Apr 8, 2025Locations: 1
Eligibility criteria

Diagnosis of Parkinson disease

Participants who are unable to comply with study visit/testing requirements (e.g... [+10]

Status: Recruiting

Western Diet on Cardiometabolic and Immune Function

This study will implement a Western Diet (WD) to understand cardiometabolic and immune function in middle-aged adults (50- 64 years old). Vascular health, intestinal permeability, and T-cell function will be examined before, during, and after the WD. The WD is a 10-day diet and will consist of 25% of total energy from added sugars.

Participants needed: 20
Trial details
Age: 50-64Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Jul 30, 2024Locations: 1
Eligibility criteria

ability to provide informed consent [+8]

current use of medications or supplements known to lower blood triglycerides or... [+8]

Status: Recruiting

University of Delaware Parkinson's Disease Registry

The purpose of this Parkinson's Disease Registry is to assist with recruitment of willing participants into future Parkinson's disease research studies at the University of Delaware.

Participants needed: 1,000
Trial details
Age: 21-100Biological sex: AllType: ObservationalSponsor: University of DelawareUpdated: May 16, 2024Locations: 1Duration: 1 Year
Eligibility criteria

Individual 21 years old or older [+2]

Individuals with a clinical diagnosis of parkinsonism that is not considered pri... [+1]

Status: Recruiting

Testing Tactile Aids With Blind Subjects

The objective of this project is to create richer tactile aids by using materials chemistry to create tactile sensations in tactile aids, as an alternative to traditional physical bumps, lines, or textures. These materials are commonly used in household products, but have not yet been used to enrich tactile aids. Successful outcomes are primarily the accuracy with which low vision or blind subjects identify objects made from tactile coatings versus traditional tactile aids. Other outcomes include time to completion of the task, or the number of distinctive categories that participants can identify.

Participants needed: 100
Trial details
Age: 16+Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Mar 13, 2024Locations: 1
Eligibility criteria

Visual Impairment: Participants should be blind or visually impaired for greater... [+2]

Status: Recruiting

Model-informed Patient-specific Rehabilitation Using Robotics and Neuromuscular Modeling

Stroke is the third leading cause of death and the primary cause of long-term disability in the United States, affecting approximately 795,000 people each year. Hemiparesis, or unilateral weakness, is common after stroke and responsible for changes in muscle activation and movement patterns as well as declines in walking speed. It has been shown that increased walking speed directly corresponds to a higher quality of life in older adults and therefore, is often the goal of motor rehabilitation after stroke. However, there is no consensus on the best method for improving walking function after stroke and the results of post-stroke gait studies vary widely across sites and studies. Walking is one of the human's most important functions that serve survival, progress, and interaction. The force between the foot and the walking surface is very important. Although there have been many studies trying to understand this, there is a need for the development of a system that can advance research and provide new functionality. In this work, we will conduct a series of studies that attempt to analyze human gait and adaptations from different perspectives.

Participants needed: 72
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Aug 24, 2023Locations: 1
Eligibility criteria

Any neurological conditions (applicable to Group A - healthy subjects) or other... [+9]

Status: Recruiting

Online Motor Control in People With Parkinson's Disease

This study aims to better understand how people with Parkinson's control reaching movements. Specifically, we are asking how these individuals respond to different environmental perturbations. Testing includes reaching movements made within a virtual reality set-up.

Participants needed: 100
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: University of DelawareUpdated: Nov 5, 2020Locations: 1
Eligibility criteria

Age 18-85 years [+5]

Any chronic or recent upper extremity musculoskeletal conditions that affects re... [+1]