Clinical trials

37

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

Condition / disease
Location
Status: Not yet recruiting

Nanopulse Laser Therapy

The purpose of this study is to evaluate the safety and effectiveness of a novel noninvasive therapy, Nanopulse Laser Therapy (NPLT), to improve recovery following traumatic brain injury (TBI).

Participants needed: 30
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older at the time of enrollment [+4]

Patients younger than 18 years of age [+5]

Status: Recruiting

OASIS: Peer Support for T2DM in Appalachia (Peer Participant)

The goal of this clinical trial is to compare the effects of peer coaching models in older adults with unmanaged type two diabetes. The main questions it aims to answer are: * Are peer coaching models effective at promoting Type 2 Diabetes Mellitus self-management? * If effective, which facets of the peer model are most effective? Peer coaches will undergo peer coach training. * Reach out to peer participants on a weekly/biweekly time frame to discuss self-management and goal setting. Retain records of contact, topics discussed, and general notes on interactions. Researchers will compare differences in the frequency of contact, as well as how peer coaches were matched to peer participants to see if efficacy of the intervention is altered between groups.

Participants needed: 76
Trial details
Age: 55+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Jun 17, 2026Locations: 2
Eligibility criteria

Age greater than or equal to 55 years [+5]

Age less than 55 years [+5]

Status: Recruiting

OASIS: Peer Support for T2DM in Appalachia (Peer Coaches)

The goal of this clinical trial is to compare the effects of peer coaching models in older adults with unmanaged type two diabetes. The main questions it aims to answer are: * Are peer coaching models effective at promoting Type 2 Diabetes Mellitus self-management? * If effective, which facets of the peer model are most effective? Peer coaches will undergo peer coach training. * Reach out to peer participants on a weekly/biweekly time frame to discuss self-management and goal setting. * Retain records of contact, topics discussed, and general notes on interactions. Researchers will compare differences in the frequency of contact, as well as how peer coaches were matched to peer participants to see if efficacy of the intervention is altered between groups.

Participants needed: 25
Trial details
Age: 55+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Jun 17, 2026Locations: 2
Eligibility criteria

Age greater than or equal to 55 years [+5]

Age less than 55 years [+4]

Status: Recruiting

The Metabolic and Genetic Drivers of Body Composition Changes Following Weight Loss Surgery

Weight loss surgery is very good at reducing body weight but it can also cause the loss of both muscle and strength. Some patients undergoing weight loss surgery do not achieve their weight loss goals and regain the weight they lost. When this occurs, the loss of muscle and strength combined with the regain of weight can impact the individual's quality of life and ability to remain active and mobile. The purpose of this study is to understand the behavioral, biological, and genetic factors that influence the success of weight loss surgery and its impact on muscle mass. Bariatric surgery patients participating in the trial will be monitored prior to, and for a year following weight loss surgery, with data collected about their eating habits, hand grip strength, and the loss of fat, muscle, and body weight following surgery. Some patients will be additionally invited to undergo detailed metabolic assessment, where we will measure how their body uses nutrients it consumes, the composition of their body (e.g. how much lean and fat tissue they have and where it is stored), identify the bacteria living in their gut, and determine their physical performance. In all patients a small sample of gut tissue will be collected at a routine endoscopy performed in advance of weight loss surgery to identify the expression (activity) of genes in their DNA. Healthy subjects will also be recruited to allow us to compare between healthy weight individuals and those undergoing weight loss surgery. On a single occasion, the healthy volunteers will undergo the same detailed metabolic assessment performed in patients as described above. We will not examine the bacteria living in the gut of the healthy volunteers, nor will we collect gut tissue from these individuals.

Participants needed: 110
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: The University of Texas Medical Branch, GalvestonUpdated: May 22, 2026Locations: 1
Eligibility criteria

Age: 30 to 50 years at time of consent [+13]

Heart, vascular, or pulmonary disease [+32]

Status: Recruiting

Chronic Subdural Hematoma Treatment With Embolization Versus Surgery Study

The goal of this clinical trial is to test in moderately symptomatic chronic subdural hematoma (CSDH) patients if middle meningeal artery embolization (MMAE) can be used as an alternative to conventional open surgery. The main questions it aims to answer are: * Compared to open conventional surgery, does MMAE reduce the need for rescue surgery or deaths? * What is the safety of MMAE and conventional open surgery in these patients? Participants will be asked to: * Share their medical history and undergo physical examinations * Have blood drawn * Have CT scans of the head * Answer questionnaires * Undergo MMAE or conventional open surgery * Provide information about possible adverse events Researchers will compare participants in the MMAE group with those in the conventional open surgery group to see if there is a reduced need for rescue surgery or deaths and evaluate safety.

Participants needed: 520
Trial details
Age: 40-90Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: May 22, 2026Locations: 31
Eligibility criteria

Age 40-90 years inclusively. [+5]

Secondary cause apart from trauma for the qualifying SDH, such as an underlying... [+24]

Status: Not yet recruiting

Sildenafil to Prevent and Reduce Cancer Related Cognitive Impairment

This study is examining the effects of standard of care cancer treatment as well as a medication called Sildenafil, on the cancer associated fatigue, cognition and the gut microbiome.

Participants needed: 30
Trial details
Phase: Phase 2, Phase 3Age: 30-50Biological sex: FemaleType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: May 11, 2026Locations: 1
Eligibility criteria

Female [+5]

Untreated thyroid disorder [+15]

Status: Recruiting

Feasibility and Adherence to a Technology-assisted Home-based Strength Training Program in Adults With Type 2 Diabetes Mellitus and Mild Cognitive Impairment

This is a single-arm feasibility study employing a pre-post design with a 12-week intervention period. The study utilizes a telehealth-assisted home-based resistance exercise program, with a structured progression from supervised to unsupervised sessions over 12 weeks.

Participants needed: 20
Trial details
Age: 55-80Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: May 11, 2026Locations: 1
Eligibility criteria

Age: 55-80 years [+5]

Diagnosis of movement disorders such as multiple sclerosis, parkinson's disease [+13]

Status: Recruiting

Vibratory Anesthesia on Pain Following Corticosteroid Injections

This research study aims to evaluate injectional pain at the site of needle insertion for corticosteroid injections (CSI) of the upper extremity depending on different modes of anesthetics. Each individual's perception of pain upon receiving a CSI with two out of three modes of anesthesia (control/no anesthesia, vibrational anesthesia, vapo-coolant anesthesia) will be utilized to compare these variables and determine the method that is associated with the least pain.

Participants needed: 165
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: May 4, 2026Locations: 1
Eligibility criteria

Any patient of the Principal Investigator who has clinically diagnosed bilateral... [+3]

Participants who opt out of the study or withdraw consent [+6]

Status: Not yet recruiting

Testing a Diabetes Care Program in Rural and Low-Income Clinics

The goal of this study is to evaluate a Community Health Worker (CHW) program for people living with diabetes in rural areas or locations that are remote from the research team. The study aims to answer the following questions: 1. Does the CHW program improve diabetes-related health outcomes, such as blood sugar control? 2. What is the sustainability of the program? 3. Is the program feasible and acceptable? Participants will be invited to attend monthly diabetes education classes led by CHWs and receive weekly mobile health check-ins from CHWs for coaching and to help coordinate care with their clinic team.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Apr 20, 2026
Eligibility criteria

Self-identified Hispanic Ethnicity [+2]

Condition known to alter HbA1c levels, e.g., recent transfusion, systemic steroi... [+3]

Status: Not yet recruiting

Nanopulse Laser Therapy

The purpose of this study is to evaluate the safety and effectiveness of a novel noninvasive therapy, Nanopulse Laser Therapy (NPLT), to improve recovery following traumatic brain injury (TBI).

Participants needed: 30
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Apr 9, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or older at the time of enrollment [+4]

Patients younger than 18 years of age [+5]

Status: Recruiting

Optimizing Gait Symmetry After Stroke Using Mechanical Constraints and Sensory Feedback

This single-session study aims to evaluate a novel gait training protocol that integrates mechanical constraints and sensory feedback to enhance paretic leg propulsion in individuals post-stroke. The study will include 15 individuals who have experienced a stroke and 15 healthy adults, each aged 20 years or older. Participants will walk on both tied-belt and split-belt treadmills under various training conditions, including backward-directed resistance (applied at the pelvis, ankle, or both) and real-time sensory feedback (visual, auditory, or combined). These interventions will be applied individually and in combination to identify the most effective environment for promoting symmetrical gait patterns. Each session will last approximately two hours. The equipment used is non-invasive, and the risk to participants is minimal.

Participants needed: 30
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Virtual Reality-Integrated Propulsion Feedback for Stroke Rehab

This study evaluates a novel Virtual Reality (VR)-integrated visual feedback system designed to enhance limb propulsion during robot-assisted gait rehabilitation in individuals post-stroke. In collaboration with CUREXO, a rehabilitation robotics company, the system is embedded within the Morning Walk® end-effector robot and provides real-time visual feedback to facilitate symmetrical use of the paretic and non-paretic limbs. The goal is to address gait asymmetry commonly observed in hemiparetic stroke survivors by promoting improved paretic leg propulsion, which is a key contributor to forward movement during walking. A total of 30 participants (15 stroke, 15 healthy controls) aged 20 years or older will undergo single-session gait training using the VR-robot system. Participants will be assessed using spatiotemporal gait parameters, muscle activity, foot pressure, and vertical ground reaction forces. Additional safety measures-including a saddle-type weight support and real-time heart rate monitoring via smartwatch-are implemented to ensure a safe and controlled training environment. This study aims to test the feasibility and effectiveness of this VR-based system in improving gait symmetry and functional walking capacity in people recovering from stroke.

Participants needed: 30
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Apr 1, 2026Locations: 1
Eligibility criteria

Adults aged 20 years or older. [+2]

Individuals with a life expectancy of less than one year. [+11]

Status: Not yet recruiting

Feasibility of A Smartphone Application Intervention in Community Settings: A Pretest-Posttest Pilot Study

The objective of this project is to test the feasibility of using a smartphone app in a community setting through collaborating with community-based organizations. The app is called utmbHealthyBrain and it has three activities: (1) drawing, (2) Tai-Chi and meditation, and (3) prayer reading. It also has a "share" function to enable users to interact with their family and friend. These activities can be translated to humans' well-beings such as a more stable emotion, more muscle movement, and better social engagement. This app does not collect any personal data and users are not required to register an account either. The overall study period is 6 weeks including one introduction session (week 1), four weeks of intervention (week 2 to 5), and final feedback session (week 6).

Participants needed: 40
Trial details
Age: 50-100Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Individuals aged 50+ who has a primary source of assistance (no age limitation f... [+3]

People who are diagnosed with any middle to severe cognitive symptoms (dementia... [+2]

Status: Recruiting

Tirzepatide to Slow Biological Aging

This pilot clinical study aims to investigate the potential effects of tirzepatide on biological aging in older adults. In this novel study, 90 adults aged 55-70 years with an indication for tirzepatide weight-loss therapy will be randomized to receive either tirzepatide 2.5 mg subcutaneously (SC) weekly or no drug for 24 weeks, followed by 12 weeks off the drug. Since tirzepatide is already recognized as a highly effective weight-loss agent in this population, the primary focus will not be on measuring weight loss. Instead, the study will document the effects of tirzepatide on markers of aging, physical function, and overall health.

Participants needed: 90
Trial details
Phase: Phase 2Age: 55-70Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Mar 24, 2026Locations: 1
Eligibility criteria

Age 55-70 years [+3]

BMI >35 kg/m² [+18]

Status: Recruiting

Pain Intervention With Needling: Pilot Of Integrated Neuromodulation Techniques

The study's purpose is to determine the effects of three different dry needling sessions on pain and quality of life for those with chronic low back pain. Dry needling is a therapeutic procedure in which a very thin, monofilament needle is inserted through the skin to reach a target tissue like a muscle to help reduce pain, improve muscle activation, and increase blood flow. Dry needling has also been shown to improve nervous system function.

Participants needed: 42
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

Both males and females between the ages of 18 and 65 will be included in this st... [+2]

Individuals who are currently seeking any form of medical treatment for lumbar c... [+5]

Status: Recruiting

Impact of a Telerehabilitation Program With Technology Enhancement on Post-burn Recovery

The purpose of this study is to examine the effect of participating in a tele-rehabilitation program after a burn.

Participants needed: 30
Trial details
Age: 18-79Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Mar 6, 2026Locations: 1
Eligibility criteria

Adults: ≥18 to ≤79 years of age [+5]

Any medical condition that, in the opinion of the investigator or physician, wou... [+3]

Status: Recruiting

Improving Sleep In Midlife Women

This study purpose of this study to see how consuming pistachios and completing a health intervention session a study therapist may improve sleep health in midlife women with poor sleep. Participants in this study will be asked to consume a study snack for about one month, complete a health education session with a study therapist and record information about their sleep. At baseline and after the intervention we will collect information about sleep, alertness, body composition, and blood lipids.

Participants needed: 72
Trial details
Age: 45-65Biological sex: FemaleType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Mar 3, 2026Locations: 1
Eligibility criteria

All races and ethnic backgrounds [+7]

Pregnancy or lactation [+9]

Status: Recruiting

Risk of Acute Complications With Rocuronium vs Cisatracurium in Patients With Chronic Kidney Disease

The purpose of the study is to determine which combination of neuromuscular blocking agent and reversal agent is safer to use during anesthesia for patients with chronic kidney disease. The main question it aims to answer is "The use of Cisatracurium with neostigmine leads to less post-operative pulmonary complications than Rocuronium with sugammadex."

Participants needed: 490
Trial details
Phase: Phase 4Age: 18-80Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Feb 23, 2026Locations: 1
Eligibility criteria

The subject is able and willing to provide and sign informed consent [+3]

Any patient under the age of 18 [+9]

Status: Recruiting

Stimulation of External Carotid Artery Circulation

This study is testing a new approach to help people with migraine headaches. Researchers want to find out if using electrical stimulation to affect blood flow in the external carotid artery is safe and practical for helping control headaches. The goal of the study is to determine whether this approach could improve headache symptoms and overall outcomes for people with migraines.

Participants needed: 12
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Age ≥18 [+2]

Known allergies to lidocaine [+9]

Status: Not yet recruiting

Leveraging Video Logs as a Bridge to Pre-exposure Prophylaxis (PrEP) With Tailored Messaging to Black Women and Their Healthcare Providers in Texas.

The primary objective of this R34 proposal is to increase willingness for PrEP initiation and PrEP initiation among Black Women (BW) and increase willingness to prescribe/refer pre-exposure prophylaxis (PrEP) to CBW among healthcare providers (HCPs) in Houston/Harris County, a high priority Ending the HIV Epidemic (EHE) jurisdiction.

Participants needed: 78
Trial details
Phase: Early Phase 1Age: 18-99Biological sex: FemaleType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Feb 17, 2026Locations: 1
Eligibility criteria

be a woman [+19]

Status: Not yet recruiting

Identification of Neuromusculoskeletal Variables Associated With Injury Risk and Performance in High School Athletes.

The purpose of this study is to complete a neuromuscular performance assessment of high school athletes who are participating in school based pre-season strength and performance training program. The performance assessment will screen for existing muscle imbalances and strength deficits known to increase risk for sports injury, and provide a baseline performance measurement. Athletes will be measured before the start of the program and then again at the end of the pre-season training period to measure changes in motor coordination, muscle strength, and performance and injury risk category. Internal and external training load will be measured weekly during the training program to track intensity of the training program. In addition to the pre and post measurements, sports injury occurrence and time away from sports participation will be tracked throughout the sport season/school year to evaluate training program outcomes and accuracy of risk assessment.

Participants needed: 250
Trial details
Age: 14-18Biological sex: AllType: ObservationalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

athletes who have completed a pre-participation sports physical [+2]

athletes who have not submitted a pre-participation sports physical to the high... [+4]

Status: Recruiting

Infusion of Lidocaine and Steroids in Middle Meningeal Artery for Pain in Subarachnoid Hemorrhage

The goal of this clinical trial is to learn if an infusion of lidocaine, with or without steroids, into the middle meningeal artery (MMA) helps relieve severe headaches in patients with spontaneous subarachnoid hemorrhage (SAH). It will also study the safety of this treatment.

Participants needed: 15
Trial details
Phase: Phase 2Age: 18-100Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Jan 9, 2026Locations: 1
Eligibility criteria

Age ≥18 years. [+2]

Known allergies to lidocaine or steroids. [+7]

Status: Recruiting

Promoting Intergenerational Health in Rural Kentuckians With Diabetes (PIHRK'D)

The goal of this feasibility study is to use family units as support to promote nutrition and physical activity of individuals with type 2 diabetes. The main question it aims to answer is: • How does the family structure impact the health of its members living with type 2 diabetes? Participants will be asked to; * Tell us about their access to food sources and places in the community to engage in physical activity. * A nutrition and physical activity plan will be developed for participants and their families to use for 6 months.

Participants needed: 75
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Jan 9, 2026Locations: 1
Eligibility criteria

must be diagnosed with type 2 diabetes [+2]

potential participants without consent

Status: Recruiting

THRIVE Well Cancer FDTN/Exercise_Creatine Supplementation

The study's purpose is to evaluate whether creatine supplementation can help breast cancer survivors respond quicker to exercise by improving strength, endurance, and body composition. We are seeking to compare information collected from healthy woman of the same age who have never had breast cancer to those participants who have had breast cancer and undergone chemotherapy treatment.

Participants needed: 60
Trial details
Age: 18-75Biological sex: FemaleType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Dec 24, 2025Locations: 1
Eligibility criteria

Age 18-75 years of age [+6]

Physical indications where performing exercise may be limited and/or contraindic... [+29]

Status: Recruiting

The Gut-Brain Axis During Neurorehabilitation; Prebiotic Treatment to Alter the Gut Microbiome and Neurologic Symptoms

The aim of this study is to characterize the microbiome of patients undergoing post-acute residential neurorehabilitation compared to community controls and to determine if a dietary fiber, Inulin, can create a shift in the microbiome leading to changes in fatigue and cognition.

Participants needed: 130
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Medical Branch, GalvestonUpdated: Dec 19, 2025Locations: 1
Eligibility criteria

Ages 18 and above [+29]