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NCT ID: NCT05317689 Recruiting - Healthy Clinical Trials

Comparing the Effects of Psilocin and Psilocybin in Healthy Adults

Start date: May 26, 2022
Phase: Phase 1
Study type: Interventional

To compare the physiological and psychological effects of psilocin taken orally by pill or sublingually by dissolving a tablet under the tongue to those of psilocybin taken by pill in healthy adults.

NCT ID: NCT05301608 Recruiting - Healthy Clinical Trials

Effects of Psilocybin on Electrophysiology and the Dynamic Content of Thought

Start date: March 3, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

This research study will use computerized tasks, electroencephalography (EEG), and magnetic resonance imaging (MRI) to look at how the drug psilocybin, a naturally occurring compound contained in hundreds of species of psychoactive mushrooms, changes thoughts and brain activity.

NCT ID: NCT05295654 Recruiting - Healthy Clinical Trials

Validity of the Kinectâ„¢ Sensor for Measuring Range of Motion in Patients Post-stroke and Healthy Test Subject

Start date: April 14, 2022
Phase: N/A
Study type: Interventional

The aim of this research is to investigate the validity of the Kinectâ„¢ sensor in post-stroke patients and in healthy test subjects during analytic and functional movements. Measurements will be compared with the Vicon-camera system (currently seen as the golden standard).

NCT ID: NCT05294913 Recruiting - Healthy Clinical Trials

Enhancing Emotional and Motivational Development to Support Well-being and Retention in Diverse University Students

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

Higher education is crucial for young adults in their intake of knowledge and skills to further their careers and reach their potentials. However, going through college is not necessarily an easy path. The purpose of this study is to enhance university students' well-being and educational experience by examining factors associated with stress and well-being. The investigator plans to recruit eighty participants from a large public university in the US to provide survey data and saliva samples at two waves during the data collection semester (beginning and end of the semester). Survey data will include demographic information and help gauge psychosocial factors related to stress and well-being. Saliva will be tested for two biomarkers each wave of data collection, cortisol (sampling three times a day for diurnal patterns for two consecutive days) and c-reactive protein, which indicate physiological stress/immune responses. Additionally, participants be randomly assigned to an intervention (n = 40) or control group (n = 40), where the intervention group will undertake a brief intervention focused on motivation and emotion regulation circa mid-semester and the control group will receive a placebo goal-setting short training. The investigator aims to examine whether intervention efforts can enhance end-of-semester psychological and physiological well-being, and particularly, whether students from diverse backgrounds (e.g., first-generation, low-income, and/or BIPOC) can benefit from the intervention. The investigator will use advanced quantitative data analysis (using Mplus v.8, in a structural equation modeling framework) to examine intervention efficacy and group differences. The investigator hypothesizes that those receiving the intervention will display a healthier profile at the end of the semester compared to their control group counterparts; and the investigator hypothesize students from diverse backgrounds will have significantly improved results from the intervention. The study will allow a better understanding to crucial steps towards exploring how to improve the well-being, higher-education pipeline, and retention of students with diverse backgrounds, providing insight on how each student's university experience can be improved.

NCT ID: NCT05294471 Recruiting - Healthy Clinical Trials

Fully Automated High-Throughput Quantitative MRI of the Liver

Start date: October 16, 2023
Phase:
Study type: Observational

The purpose of this research is to see if a new automated magnetic resonance imaging (MRI) method will be able to improve the images taken of the liver. Participants will have either known or suspected liver disease, known or suspected iron overload syndrome, or be a healthy adult. Participants will be in the research study for one day.

NCT ID: NCT05288881 Recruiting - Healthy Clinical Trials

Single Ascending Dose Study of ANX105

Start date: February 28, 2022
Phase: Phase 1
Study type: Interventional

This study will assess the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of single ascending doses of ANX105 administered intravenously (IV) to healthy participants.

NCT ID: NCT05279339 Recruiting - Healthy Clinical Trials

Subjective and Objective Changes in Muscle-stiffness

Start date: February 21, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate muscle stiffness in relation to delayed on-set muscle soreness following exercise and to investigate how well the change in muscle stiffness correlates with the subjective experienced degree of stiffness.

NCT ID: NCT05273203 Recruiting - Healthy Clinical Trials

The Influence of Football Training as a medicine_FIM_UTH

FIM
Start date: January 31, 2022
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled study will be to inestigate the relationship between recreational football training at various training volumes and the health responses of middle-aged participants at high risk for metabolic and / or cardiovascular disease.

NCT ID: NCT05264727 Recruiting - Healthy Clinical Trials

Glucagon Suppression by Hyperglycemia in the Presence and Absence of Amino Acid Infusion

Start date: May 30, 2023
Phase: Phase 4
Study type: Interventional

This study is being done to better understand how amino acids alter the release of glucagon and insulin compared to glucose alone in health and disease.

NCT ID: NCT05264142 Recruiting - Healthy Clinical Trials

Risk of CYP2C19 Phenoconversion in Healthy Volunteers With Rapid, Normal, and Intermediate Predicted Metabolizers' Status

Switch19
Start date: April 1, 2022
Phase: Phase 1
Study type: Interventional

CYP2C19 is responsible for the metabolism of approximately 10% of drugs currently on the market, including several proton pump inhibitors, clopidogrel, benzodiazepines and some tricyclic antidepressants, including amitriptyline. It is a cytochrome whose activity is characterized by a great variability in the general population. This variability can be explained, in part, by genetic and environmental factors The classification of phenotypes associated with CYP2C19 has evolved over time. Today, five distinct phenotypes are used to characterize this variability: the slow metabolizer (SM) phenotype, the intermediate metabolizer (IM) phenotype, the normal metabolizer (NM) phenotype, the fast metabolizer (RM) phenotype and finally the ultra-fast metabolizer (UM) phenotype. (UM) phenotype. Although directly measurable with test substances, CYP2C19 phenotypes are often assigned on the basis of genotype. They may be impacted by intrinsic (e.g., comorbidities) or extrinsic (e.g., co-medications) factors. Phenoconversion or phenotypic change is the phenomenon by which an individual switches from one phenotype to another due to an environmental influence such as a drug interaction. However, genotype is likely to influence the degree of response to a drug interaction. Vulnerability to phenoconversion therefore differs according to the genotype of the individual. The purpose of our study is to determine whether individuals genetically MR, NM and IM have the same vulnerability to phenoconversion. Thus, the magnitude of the response to CYP2C19 inhibition will be studied in these 3 groups of individuals (NM:*1/*1, RM:*1/*17 and IM:*1/*2-*2/*17). Inhibition will be studied in two steps, using a strong (fluvoxamine) and a weak (voriconazole) inhibitor of CYP2C19.