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NCT ID: NCT05674292 Completed - Clinical trials for Circumference Reduction

An Evaluation of the Effect of the Erchonia Corporation Violet Zerona® Z6 for Body Contouring

Start date: July 11, 2022
Phase: N/A
Study type: Interventional

The purpose of this clinical study is to determine the effectiveness of the Erchonia® Violet Zerona Z6 (manufactured by Erchonia Corporation (the Company), an over-the-counter (OTC) laser device, in providing noninvasive body circumference reduction.

NCT ID: NCT05674188 Completed - Augmented Reality Clinical Trials

AR vs In Person Simulation for Medical Workplace Training

Start date: March 20, 2023
Phase: N/A
Study type: Interventional

This study will evaluate the physiologic and emotional effects of an augmented reality (AR) simulation versus an in-person simulation. This is a single institution, non-inferiority, randomized controlled trial. The target enrollment will be 100 participants in each group for a total of 200 participants. One group will wear an AR headset and participate in an AR medical crisis scenario and the other group will participate in the same scenario with a traditional, mannequin based in situ simulation.

NCT ID: NCT05674136 Completed - Healthy Clinical Trials

Clinical Equivalence of Masimo INVSENSOR00061 to RD SET Neo

Start date: November 18, 2022
Phase: N/A
Study type: Interventional

This study is designed to compare the equivalence of the Masimo INVSENSOR00061 to RD SET Neo for SpO2 and performance of PR and RRp as the subjects undergo a controlled desaturation protocol. This type of study design is required to evaluate the performance of pulse oximeters based upon the ISO 80601-2-61 standard which is also adopted and referenced by the FDA.

NCT ID: NCT05674123 Completed - Colorectal Neoplasm Clinical Trials

Evaluating the Safety and Effectiveness of the Flex Robotic System for the Surgical Removal of Colorectal Lesions

Start date: January 15, 2020
Phase: N/A
Study type: Interventional

This clinical trial assesses the safety and effectiveness of a new device called the Flex Robotic System in the surgical removal (resection) of colorectal lesions. When an area of abnormal tissue called a lesion is found in the colon or rectum, it is often not known if the lesion is cancerous or non-cancerous. Recommendation to remove the lesion may be made. Current methods of resection can be challenging and time-consuming. The Flex Robotic System is a new device that provides a stable working environment, better ability to grasp and cut lesions, and better tissue handling when performing a resection. The Flex Robotic system may be more effective at removing colorectal lesions than standard resection techniques.

NCT ID: NCT05673603 Completed - Renal Impairment Clinical Trials

A Study of Brensocatib Following a Single Oral Administration in Participants With or Without Renal Impairment

Start date: July 20, 2021
Phase: Phase 1
Study type: Interventional

The primary purpose of the study is to determine the pharmacokinetics (PK) following a single oral dose administration of brensocatib, safety, and tolerability of brensocatib when administered to participants with impaired renal function and in healthy participants.

NCT ID: NCT05673317 Completed - Breastfeeding Clinical Trials

A Technological Approach to Improved Breastfeeding Rates and Self-Efficacy

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

To provide patients with easily accessible information in the form of a smartphone application regarding medically appropriate information about breastfeeding and to assess the impact this information has on women's breastfeeding rates and perception of self-efficacy (primary outcome).

NCT ID: NCT05673174 Completed - Healthy Clinical Trials

Avicena LVDP Validation Study in Healthy Volunteers

Start date: June 16, 2022
Phase:
Study type: Observational

The purpose of this study is to document the utility of the Vivio System in quantifying LVDP in healthy volunteers.

NCT ID: NCT05672953 Completed - Oral Microbiome Clinical Trials

Biogeography of the Oral Microbiome

Start date: May 20, 2021
Phase:
Study type: Observational

A cross-sectional study to metatranscriptomically analyze and compare the oral microbiome in different environmental niches within the oral cavity.

NCT ID: NCT05672771 Completed - Cognitive Aging Clinical Trials

The Effects of Mixed Working Memory Training on Subsequent Training Gains Among Older Adults

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

While an intellectually active and socially integrated lifestyle shows promise for promoting cognitive resilience, the mechanisms underlying any such effects are not well understood. The aim of the current project is test the implications of the "mutualism" hypothesis, which suggests that intellectual function emerges out of the reciprocal influence of growth in abilities as they are exercised in the ecology of everyday life. Such a view implies that improvement in one component will enhance the modifiability of a related component. An additional aim was to test the idea that mutualistic effects will be enhanced by more diverse training in related skills, such as interleaved training of multiple skills, relative to single-component training. A "successive-enrichment" paradigm was developed to test this with working memory (WM) as the target for training given its centrality in models of attention, intellectual function, and everyday capacities such as reasoning and language comprehension. All participants receive the same target training, but the nature of the training that precedes it is manipulated. Outcome measures include pre- to posttest gains in working memory and episodic memory, as well as the rate of gain in learning the target task. The principle of enhanced mutualism would predict that more diverse experiences related to the target skill will enhance efficiency in acquiring the target skill.

NCT ID: NCT05672745 Completed - Clinical trials for To Understand the Characteristics of Digital Mental Health Intervention Users as They Relate to Mental Health Outcomes

How Phenotypical Characteristics of Woebot Users Are Related to Clinical Outcomes

Start date: May 11, 2022
Phase: N/A
Study type: Interventional

The goal of this observational study is to understand the characteristics of Woebot users as they relate to clinical outcomes. The objectives it aims to address are: 1. To assess Woebot usage patterns, satisfaction ratings, self-efficacy, stress, resilience, work productivity and activity impairment, alexthymia, and bond over time based on demographic, clinical baseline levels, and attitudinal characteristics 2. Among users who present with clinical levels of anxiety or depression, to assess the contribution of demographic characteristics, attitudinal characteristics, and patterns of engagement on clinical outcomes of interest over time 3. To collect and explore attitudinal characteristics of Woebot users regarding their experiences with mental health care and perceived value of digital tools for emotional support 4. Explore meaningful subgroups of Woebot users based on demographic and attitudinal characteristics, clinical outcomes, and patterns of engagement Participants who meet study eligibility requirements will be: - invited to engage with the Woebot Life program for 8 weeks - complete survey assessments at day 3, week 4 (mid-intervention), and week 8 (end of intervention)