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NCT ID: NCT04590040 Completed - Dentin Sensitivity Clinical Trials

Trial of Nano-hydroxyapatite-Containing Toothpastes for Relief of Dentin Hypersensitivity

Start date: July 28, 2020
Phase: N/A
Study type: Interventional

Subjects will be enrolled into 3 balanced groups each using a different strength toothpaste. Dental hypersensitivity (DHS) will be assessed at study start, midway and study end.

NCT ID: NCT04589962 Completed - Clinical trials for Surgical and the Percutaneous Approach to the Upper Extremity Access

SUrgical Versus PERcutaneous AXillary Artery International Registry

Start date: October 9, 2020
Phase:
Study type: Observational

The purpose of the Study is to compare the outcomes of the surgical and the percutaneous approach to the upper extremity access (axillary or brachial artery) during endovascular procedures on the aortic valve, the aorta, and its side branches.

NCT ID: NCT04589676 Completed - Opioid Overdose Clinical Trials

Developing and Testing the Opioid Rapid Response System

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

This Phase I SBIR will develop and demonstrate the usability/feasibility of the Opioid Rapid Response System (OSSR) in order to reduce deaths and strain on emergency response systems from opioid overdoses.

NCT ID: NCT04589611 Completed - Osteoarthritis Clinical Trials

Translating Metabolic Responses to Mechanical Insult Into Early Interventions to Prevent PTOA

Start date: July 20, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

This is a small-scale proof-of concept clinical trial of amobarbital as a treatment to prevent post-traumatic osteoarthritis in fractured ankle joints. The study is a double blind, prospective, randomized, placebo-controlled, stepwise trial. Amobarbital will be delivered to ankle joints in solution with hyaluronic acid (HA) as a vehicle. Amobarbital/HA injections (active dose) will be compared to HA alone (placebo dose). Our primary goal is to confirm safety, but we will also assess whether treatment improves chondrocyte viability and decreases synovial inflammation. The intervention that will be utilized has proven to be effective using vitro and in vivo models. The study team will assess safety and begin to evaluate efficacy of amobarbital/Gel-One in patients having sustained tibial pilon fractures. The study team will use advanced imaging-based methods we have developed to characterize how joints subjected to varying levels of fracture severity and residual elevated contact stress respond in treated and control groups.

NCT ID: NCT04589559 Completed - Cardiac Arrest Clinical Trials

The Care After Life-threatening Medical Events Study

CALME
Start date: November 23, 2020
Phase: N/A
Study type: Interventional

This study tests the feasibility of a home-based heart rate variability biofeedback (HRVB) intervention in survivors of cardiac arrest (CA). Specifically, the primary purpose of this pilot study is to assess feasibility, acceptability, appropriateness, usability, and compliance for an at-home, 3-week HRVB intervention in 10 participants. The study also tests whether cardiac-related interoceptive fear, trait anxiety, and negative affect decrease among CA survivors completing the HRVB intervention.

NCT ID: NCT04589520 Completed - Stress Clinical Trials

The Effects of the App HeartBot on the Stress and Emotional Well-Being Over a 21-day Challenge

Start date: August 18, 2019
Phase: N/A
Study type: Interventional

HeartBot is an app designed to enable people 14 years and older to use relaxation tools offered by Heartfulness. The study is conducted to examine the effect of the app on stress and emotional wellness in participants 14 years and older. Research Question: Does HeartBot affect the stress levels and emotional wellness in participants 14 years and older? Hypothesis: Participants who use HeartBot for 21 days will see a significant decrease in their stress levels and an improvement in emotional wellness.

NCT ID: NCT04589377 Completed - Stress Clinical Trials

Mindfulness to Mitigate Psychological Threat and Improve Engagement and Learning in Introductory Physics Courses

Start date: October 26, 2020
Phase: N/A
Study type: Interventional

This project involves testing a brief mindfulness training program to reduce students' psychological threat and support motivation, engagement, and learning in introductory undergraduate physics courses. The investigators predict that, compared to a control condition, mindfulness training will reduce psychological threat and increase motivation, engagement, and learning in physics.

NCT ID: NCT04589286 Completed - Multiple Myeloma Clinical Trials

Randomized Study of Digital Life Coaching in Myeloma Patients Undergoing Transplantation

Start date: December 29, 2020
Phase: N/A
Study type: Interventional

Autologous stem cell transplantation (SCT) is the standard of care for fit multiple myeloma (MM) patients; however, the first 100 days after SCT are marked by extensive life disruptions. We have found a 56% relative increase in the use of high-risk benzodiazepine and Z-class (B/Z) drugs for anxiety and insomnia among MM patients during this period. Digital life coaching (DLC), whereby trained coaches work longitudinally with patients through phone calls and text messages to accomplish personal goals, may be able to target anxiety and insomnia in a more integrative manner. This study will investigate whether peri-SCT DLC can lower B/Z usage and improve patient-reported well-being.

NCT ID: NCT04589195 Completed - Cognitive Change Clinical Trials

Measuring Mindfulness Application

Start date: October 11, 2021
Phase: N/A
Study type: Interventional

The purpose of the research study is to learn more about how ROTC cadets may engage with mindfulness training program content that is delivered through a smartphone or website application. Mindfulness training program content includes mindfulness practices that foster attention and awareness.

NCT ID: NCT04589117 Completed - Clinical trials for Parents During COVID-19

Expressive Writing for COVID-19 Resilience for Parents

Start date: May 27, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the impact of a 4-week, virtually-delivered expressive writing intervention on resilience in a cohort of parents and caregivers currently navigating the COVID-19 pandemic during spring & summer of 2020.