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NCT ID: NCT04843228 Completed - Perfectionism Clinical Trials

Cognitive Bias Modification for Perfectionism and Intolerance to Uncertainty

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

This study will examine the impact of cognitive bias modification (CBM) on perfectionism and intolerance to uncertainty. Undergraduate students will be recruited and randomly assigned to either experimental or placebo-control groups. Each group will attend four sessions of CBM over four weeks.

NCT ID: NCT04843163 Completed - Clinical trials for Mental Disorder, Child

Examining the Impact of a Peer-Provided Psychoeducational Program for Parents: NAMI Basics

Start date: December 6, 2017
Phase: N/A
Study type: Interventional

This study will evaluate a peer service program for caregivers of youth struggling with mental illness using a program developed by the National Alliance on Mental Illness (NAMI) called NAMI Basics. This peer service program for caregivers was adapted from their successful and empirically supported model for caregivers of adult children with mental illness (Family-to-Family). The child-focused intervention, NAMI Basics, is a six-class curriculum focused on increasing caregiver knowledge about mental illness, empowering parents to advocate for their children across service systems, and introducing skills that assist in family problem-solving and communication. The current study is a randomized effectiveness trial of NAMI Basics. Caregivers who are parenting youth with a mental illness (N = 175) referred to the NAMI Basics program through natural referral routes will be given the option to participate in the study, and if interested, randomly assigned to either an immediate NAMI Basics classes (Wave A) or an 8-week delay condition (Wave B), followed by initiation of the NAMI Basics class.

NCT ID: NCT04842747 Completed - SARS-CoV Infection Clinical Trials

VERU-111 in the Treatment of SARS-Cov-2 Infection by Assessing Its Effect on the Proportion of Patients Who Die on Study

VERU-111
Start date: May 18, 2021
Phase: Phase 3
Study type: Interventional

To demonstrate the efficacy of VERU-111 in the treatment of SARS-Cov-2 Infection by assessing its effect on the proportion of patients who die on study (prior to Day 60).

NCT ID: NCT04842123 Completed - Atrial Fibrillation Clinical Trials

Electrocardiogram Clinical Validation Study

Start date: March 31, 2021
Phase: N/A
Study type: Interventional

The purpose of the study is to confirm the Garmin ECG (electrocardiogram) software algorithm can detect and classify atrial fibrillation and normal sinus rhythm on single lead ECG data derived from a Garmin wrist-worn, consumer device. The study will also confirm the software's ability to create a Lead I ECG that is clinically equivalent to a reference device. The Garmin ECG software is not a diagnostic system and is intended for informational purposes only.

NCT ID: NCT04842110 Completed - Abdominal Obesity Clinical Trials

Eon™ FR 1064 Full Abdomen Clinical Study Protocol

Start date: August 24, 2019
Phase: N/A
Study type: Interventional

This is a marketing study intended to provide additional data for marketing purposes for the eon™ FR is FDA 510(k) which has been cleared for non-invasive lipolysis of the abdomen to achieve disruption of adipocyte cells intended for non-invasive aesthetic use to achieve a desired aesthetic effect. This device is intended for individuals with a Body Mass Index (BMI) of 30 kg/m2 or less.

NCT ID: NCT04842045 Completed - Amnesia Clinical Trials

Pilot RECAP Study in Healthy Volunteers

RECAP
Start date: May 21, 2021
Phase: Phase 1
Study type: Interventional

The primary objective of the RECAP Study Program is to investigate the role played by conscious experience in the antidepressant effects of the psychedelic agent psilocybin. This pilot dosing study (PILOT RECAP) is designed to determine the optimal dose of midazolam that allows a psychedelic experience to occur while inducing amnesia for the experience. This is an essential step required for subsequent evaluation of the role of memory for the psychedelic experience in the antidepressant effects of psilocybin in the full RECAP study.

NCT ID: NCT04841967 Completed - Parenting Clinical Trials

Feasibility Trial of the TELL Tool Intervention

Start date: July 26, 2021
Phase: N/A
Study type: Interventional

A radical paradigm shift is taking place where technology, notably the explosion in easy accessible direct-to-consumer genetic testing (e.g., 23andMe) and a high consumer interest in genealogy (e.g., Ancestry.com), has hijacked gamete (eggs, sperm) and embryo donation recipient parents' control over whether to inform their children about their donor conception. Historically, the practice of gamete donation has been shrouded in secrecy, however, the skyrocketing use of direct-to-consumer genetic testing means that at any point in an adult life, an uninformed donor-conceived person can learn their DNA does not match their presumed ancestry of their parents and family members, putting into question their genetic relatedness to their parents and launching a spiraling sequence of negative health consequences and trauma. Furthermore, the lack of one's knowledge about actual genetic heritage in the age of precision medicine can be enormously detrimental to health and can result in medical maltreatment, including death. To address this serious problem and in accordance with International Patient Decision Aid Standards, we developed a digital, tailored, multicomponent Tool to Empower ParentaL TeLling and Talking (i.e., TELL Tool). The objective of this R34 study is to examine the feasibility, acceptability, and preliminary effects of the TELL Tool intervention in a pilot randomized-controlled feasibility trial with 60 donor-recipient parents and 10 clinicians to determine intervention viability and inform a larger, efficacy trial. An eBook with content about good parenting principles serves as the attention control.

NCT ID: NCT04841707 Completed - Covid19 Clinical Trials

Total-Body Parametric 18F-FDG PET of COVID-19

Start date: May 10, 2021
Phase: N/A
Study type: Interventional

The primary objective is to measure the change between COVID-19 patients and normal subjects; the secondary objective is to measure the change in COVID-19 patients between baseline and 4-month follow up.

NCT ID: NCT04841629 Completed - Clinical trials for User Acceptability of Gel Delivery System

Perception & Acceptability of a Cervical Cancer Prevention Prebiotic Device

Start date: February 24, 2022
Phase: N/A
Study type: Interventional

PreBioGyn will be compared to market leading vaginal pH buffering gels using established forearm test methods associated with vaginal lubricity sensation in 42 women. Women will also rate each gel for smell and appearance using established methods. The PreBioGyn gel enclosure and intravaginal applicator design will be evaluated for: look and feel, ability to prepare for dosing, ability to expulse dose, and likelihood of future use by subjects. Open-ended feedback on the gel and applicator will occur to gather contributions for each product.

NCT ID: NCT04841551 Completed - Adiposity Clinical Trials

Kybella for the Treatment of Flank Fat (FF)

Start date: July 22, 2021
Phase: Phase 4
Study type: Interventional

To Determine the safety and Effectiveness of Kybella for the treatment of Flank Fat (FF)