Clinical trials

5

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

Cannabis and Opioid Use Disorder, Study 2

This inpatient study enrolls healthy individuals who have opioid use disorder. Participants live at the University of Kentucky Hospital for approx. 6 weeks. During this time, we will examine how repeated doses of oral cannabis and acute doses of oral and inhaled cannabis 1) modify the intensity and time course of opioid withdrawal, 2) modify the effects of intranasal opioid administration and 3) impact the safety of opioid administration.

Participants needed: 100
Trial details
Phase: Phase 1Age: 18-55Biological sex: AllType: InterventionalSponsor: University of KentuckyUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Participants with moderate to severe opioid use disorder

Individuals who do not use opioids or do not experience opioid withdrawal when t...

Status: Recruiting

Recovery of Physical Function After Critical Illness In Older Adults

The proposed study is a prospective, observational study assessing the recovery of muscle and physical function in patients surviving critical illness (n =150) at hospital discharge (baseline) and repeated serially. Patients will be enrolled after life-saving modalities have been weaned near hospital discharge. Patients will participate in testing at baseline, 3-, 6-, 12-, and 24-months after hospital discharge. In a subset of patients (n = 18), muscle biopsies will be performed at baseline and then repeated once at either 12- or 24-months after hospital discharge.

Participants needed: 150
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: University of KentuckyUpdated: May 28, 2026Locations: 1
Eligibility criteria

adult patients (≥40 years of age) [+2]

individuals who were not ambulatory prior to ICU admission, [+3]

Status: Not yet recruiting

Comparing Acupuncture vs. Sham Acupuncture for the Management of Hot Flashes in Prostate Cancer Patients Receiving Hormone Therapy

This study is evaluating whether acupuncture may help reduce hot flashes in men receiving hormone therapy for prostate cancer. Hot flashes are a common side effect of androgen deprivation therapy (ADT) and may negatively affect sleep, mood, concentration, daily activities, and overall quality of life. Participants enrolled in this study will receive acupuncture treatment over a defined treatment period. The study will assess changes in hot flash frequency, severity, and quality of life using patient questionnaires and symptom diaries. Participants will complete a daily hot flash diary during selected 7-day assessment periods and quality-of-life questionnaires during study visits. The primary goal of this study is to determine whether acupuncture may improve hot flash symptoms and related quality of life in men undergoing treatment for prostate cancer.

Participants needed: 40
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: University of KentuckyUpdated: May 27, 2026Locations: 1
Eligibility criteria

Patients with history of prostate cancer with currently receiving hormone therap... [+9]

Patients can't travel for acupuncture [+1]

Status: Recruiting

Auditory Biofeedback Gait Training Individuals With Chronic Ankle Instability

The goal of this randomized clinical controlled trial is examine the effects of gait training with auditory biofeedback (AudFB) on gait biomechanics, clinical measures of ankle joint health, and patient-centered outcomes. The following specific aims will achieve this objective: * Specific Aim 1: Determine if a 6-week gait training with AudFB intervention improves lower extremity biomechanics compared to a Control condition in participants with CAI. * Specific Aim 2: Determine if a 6-week gait training with AudFB reduces talar cartilage deformation compared to a Control condition in participants with CAI. * Specific Aim 3: Determine if a 6-week gait training with AudFB reduces episodes of ankle giving-way and reduces self-perceived severity of symptoms relative to a Control condition in participants with CAI. Participants will: * Complete 12 intervention sessions over a 6-week period of walking, ruck marching, and runninig. * Complete testing sessions before and after the intervention, then after 6 and 12-months following the intervention.

Participants needed: 100
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: University of KentuckyUpdated: Oct 7, 2025Locations: 2
Eligibility criteria

Physically active adults (defined as participants reporting a score of =4 on the... [+3]

an ankle sprain in the previous four weeks or lower extremity neuromusculoskelet... [+6]

Status: Recruiting

TRAC-ER Intervention to Reduce Risky Alcohol Use and HIV Risk

Ecological momentary interventions (EMI), which use phones to deliver messages to reduce alcohol use and related risk behaviors during or prior to drinking events, can help to address triggers in real-time. GPS tracking can determine when individuals visit places they have previously reported drinking or triggers to drink and then EMI messages can be delivered upon arrival to prevent risky alcohol use. A mobile app has been developed that uses GPS tracking to determine when individuals visit "risky" places and then delivers a survey asking what behaviors they engaged in while at the location. The goal of the proposed study is to use this app to enhance the Tracking and Reducing Alcohol Consumption (TRAC) intervention by delivering messages that encourage participants to employ strategies discussed during TRAC sessions when arriving at risky places. When they leave these places, they will complete a survey and breathalyzer reading in order to collect event-level self-report and biological data on alcohol use and HIV risk. If their breathalyzer result indicates alcohol use, they will receive harm reduction messaging. It is expected that combining TRAC with EMI ("TRAC-ER") will increase effectiveness by reinforcing topics discussed during these sessions, providing in-the-moment messaging to address triggers, and collecting real-time alcohol use data.

Participants needed: 405
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: University of KentuckyUpdated: Mar 30, 2025Locations: 2
Eligibility criteria

is between the ages of 18-35 at the start of the study [+4]

do not speak English [+2]