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NCT ID: NCT04181463 Not yet recruiting - Malignant Neoplasm Clinical Trials

Nasal Inhalation of Isopropyl Alcohol for the Treatment of Nausea in Patients With Cancer

Start date: December 5, 2024
Phase: N/A
Study type: Interventional

The goal of this research study is to understand the effect of inhalation approaches in reducing nausea in cancer patients.

NCT ID: NCT04176471 Not yet recruiting - Clinical trials for Neonatal Encephalopathy

TIME Study: Therapeutic Hypothermia for Infants With Mild Encephalopathy

TIME
Start date: May 1, 2020
Phase: N/A
Study type: Interventional

The TIME study is a randomized, controlled trial to evaluate impact on early measures of neurodevelopment and the safety profile of therapeutic hypothermia in term neonates with Mild Hypoxic-Ischemic Encephalopathy who are < 6 hours of age. Neurodevelopmental outcome will be assessed at 12-14 months of age. The study will enroll 68 neonates randomized to therapeutic hypothermia or normothermia across 5 centers in California.

NCT ID: NCT04173559 Not yet recruiting - Pregnancy Related Clinical Trials

Sleep and Tracking Effects in Pregnancy Study

STEP
Start date: May 2023
Phase: N/A
Study type: Interventional

Purpose: The investigators hypothesize that a simple, personalized, smartphone-based activity intervention using a wrist-based activity tracker will help high risk pregnant women reduce their stress during pregnancy. Participants: Pregnant women enrolled in prenatal care at the University of North Carolina who have a documented moderate or high level of perceived stress ( ≥ 14) and are at high risk for adverse pregnancy outcomes due to body mass index of ≥ 30 kg/m2 or history of gestational hypertension, preeclampsia, intrauterine growth restriction, or preterm birth <37 weeks' in a prior pregnancy. Procedures: Women meeting inclusion criteria will be recruited through the University of North Carolina prenatal care clinics. They will be contacted for possible participation at regularly scheduled prenatal visits and/or ultrasound. They may also be contacted for possible participation by remote methods (e.g., Telehealth). Women who are enrolled will complete validated dietary, stress, sleep, and body image questionnaires. Enrolled women will then be randomized to receive standard obstetrical care or enhanced counseling. All participants will receive a wrist-based activity tracker. Maternal blood sample for biochemical markers of stress and gene expression will be obtained at the initial visit; a followup blood sample will be obtained later in pregnancy, and a small portion of the placenta saved at delivery. Maternal and neonatal outcomes will be compared between groups.

NCT ID: NCT04168697 Not yet recruiting - Bipolar Disorder I Clinical Trials

Effect of Behavioral Intervention on Cannabinoid Receptors in BAD

WHM_BAD
Start date: February 1, 2020
Phase: N/A
Study type: Interventional

The objective of this study is to determine whether the practice of a non-drug related intervention technique (behavioral modification technique consisting of a combination of breathing exercises, cold exposure and meditation) has an effect on long-term cannabinoid receptor function in a control group as well as in a group of patients suffering from bipolar affective disorder (BAD). Specifically, the objective of this study is to test whether the applied behavioral modification technique is able to alter cannabinoid receptor density in brain areas that modulate mood and motivational drive (such as vmPFC, PAG, VTA, amygdala and OFC). The investigators believe that these studies will form the impetus for a better understanding and deployment of non-drug related treatment methods in patients with various depressive symptoms. In particular, it appears that the proposed behavioral modification technique might be a powerful, currently under-appreciated, method to positively modulate the brain's own cannabinoid system.

NCT ID: NCT04158037 Not yet recruiting - Gambling Disorder Clinical Trials

Don't Go There: A Geospatial mHealth App for Gambling Disorder

Start date: June 2024
Phase: N/A
Study type: Interventional

The goal of this project is to develop and to test the efficacy of a novel mHealth app for gambling disorder. The app capitalizes on smartphones' global positioning software (GPS) that recognizes a user's location to within 15 feet. Users will receive an alert of this go near a gambling venue. The project will conduct a 12-week pilot randomized clinical trial to test the short-term efficacy of the app with gambling disorder individuals.

NCT ID: NCT04146727 Not yet recruiting - Clinical trials for Heart Failure, Congestive

Utilizing Technology for Optimization of Pain Management and Mobilization in High Risk Cardiac Surgical ICU Patients

Start date: January 2020
Phase:
Study type: Observational [Patient Registry]

The purpose of this project is to improve mobility in the perioperative period using activity trackers to augment current practice. Delirium and poor functional status following ICU stays are intractable problems for which clear solutions do not exist. Digital health approaches have not been applied to these problems in the ICU setting and may represent a viable and unexplored intervention. The program will involve the utilization of an activity tracker in ambulating patients. There will be two arms to the program. The first will involve the longitudinal study of ambulating lung transplant patients. Patients will be given an activity tracker at time of transplant which will continue throughout their care into their first month at home. The data will be collected to identify correlation between activity and clinical outcomes.

NCT ID: NCT04145050 Not yet recruiting - Para-Athletes Clinical Trials

Carbohydrate Oxidation in Elite Wheelchair Racers During Marathon Simulation

COW
Start date: December 1, 2022
Phase: N/A
Study type: Interventional

To examine the effect of varying amounts of carbohydrate ingestion on performance, gastrointestinal experiences, and other physiological markers in elite wheelchair racers during a simulated marathon.

NCT ID: NCT04142879 Not yet recruiting - Clinical trials for Stroke Workflow and Clinical Outcome Parameters

Automated Detection and Triage of Large Vessel Occlusions Using Artificial Intelligence for Early and Rapid Treatment (ALERT)

ALERT
Start date: December 1, 2019
Phase:
Study type: Observational

Post Market, Prospective, Randomized, Controlled, multi center data collection study to evaluate the use of Viz versus the standard of care in stroke workflow and clinical outcome parameters.

NCT ID: NCT04142866 Not yet recruiting - Stroke Clinical Trials

Transcranial Direct Current Stimulation (tDCS) With Verb Network Strengthening Treatment (VNeST) in Chronic Aphasia

Start date: September 1, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to assess changes in language abilities of participants with chronic, post-stroke aphasia following an 8-week therapy period combined with brain stimulation. The investigators use a stimulation method called transcranial direct current stimulation (tDCS). The investigators cover two electrodes in damp sponges, place them on the scalp, and pass a weak electrical current between them. Some of this current passes through the brain and can change brain activity. One electrode is placed over language areas a bit above and in front of the left ear. The other is placed on the forehead above the right eye. Stimulation is provided twice a week for 8 weeks during aphasia therapy. The investigators believe that this stimulation may increase the effectiveness of therapy.

NCT ID: NCT04142398 Not yet recruiting - HIV Infection Clinical Trials

Incidence of HPV Infection and HPV-Associated Disease in Screening Indian Men Who Have Sex With HIV-Positive Men

Start date: April 30, 2025
Phase:
Study type: Observational

This research trial studies the incidence of human papilloma virus (HPV) infection and HPV-associated disease in screening Indian men who have sex with human immunodeficiency virus (HIV)-positive men. Gathering health information over time from Indian men who have sex with men (MSM) may help doctors determine how many HIV -positive MSM develop new HPV infections and how many HIV-positive MSM have HPV related disease.