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NCT ID: NCT05531396 Not yet recruiting - Healthy Clinical Trials

Agility Training on Physical Performance, Cognitive Function and Brain Activities in Elderly

Start date: September 5, 2022
Phase: N/A
Study type: Interventional

Agility comprised of cognitive and physical functions, which influences whole-body movement with change of speed and direction. Agility training is widely used in athletes, and recent studies have begun to apply it into the elderly. Agility training is multidimensional and highly functional, which makes it possible to provide more efficient training in limited time. In elderly, the decrement of cognitive function, muscle strength in the upper and lower limbs, the percentage of body fat, body flexibility and endurance caused by aging will make it difficult for the elderly to perform movements. Therefore, it is essential to explore whether agility training can achieve the improvement of the physical function and cognitive function in elderly, and to find the relationship between the two functions and brain activity. Method: This study will recruit 60 participants, and randomly allocate to control group and agility training. The training groups will have 8 weeks of training, 2 times a week, 45 minutes of training each time. Assessment will be performed before and after intervention in 1-week, and with 1-month follow-up. Assessment including agility ability, physical function, cognitive function, brain activity, and functional assessment scales.

NCT ID: NCT05531097 Completed - Healthy Clinical Trials

Ascending Single-Dose and Multiple-Dose Study to Evaluate HSK31679 in Healthy Subjects and Subjects With Elevated LDL-C

Start date: February 22, 2022
Phase: Phase 1
Study type: Interventional

This is a Phase I, single-dose and multiple dose escalation clinical trial for HSK31679 conducted in chinese healthy volunteers and LDL-C elevated subjects. The safety, tolerability, food-impact,pharmacokinetics and pharmacodynamics of HSK31679 tablet in healthy volunteers and LDL-C elevated volunteers will be evaluated using a randomized, double-blind, placebo-controlled trial design

NCT ID: NCT05528848 Recruiting - Healthy Clinical Trials

Multi-System Analysis of Opioid Receptor Binding

Start date: September 20, 2022
Phase: Phase 1
Study type: Interventional

This study will enroll up to 60 adults (including 30 females and 30 males) in three cohorts of up to 20 subjects each. In all three groups, [11C]carfentanil whole-body PET imaging will be used to examine the central nervous system (CNS) and broader systemic opioid binding in an initial scan session. In the two groups not receiving standard of care medication assisted treatment (MAT) for opioid use disorder (OUD) the effects on [11C]carfentanil binding potential of the blockade of opioid binding by the non-selective opioid antagonist naloxone administered parenterally in a second scan session will also be examined. If two scans are completed they can be done on the same day or on different days.

NCT ID: NCT05526586 Completed - Healthy Clinical Trials

A Twelve Week Study of Prototypes Mouth Rinses

Start date: August 31, 2022
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of two essential oil containing experimental mouth rinse formulations and an essential oil containing mouth rinse compared to a hydroalcohol control mouth rinse for the reduction of gingivitis and plaque when used as an adjunct to tooth brushing during a twelve-week product usage period.

NCT ID: NCT05525845 Recruiting - Healthy Clinical Trials

Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI

Start date: September 8, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate how gut hormones and brain areas respond differently to gastric distention, tasteless calories, or palatable food and how this alters appetite.

NCT ID: NCT05525468 Completed - Healthy Clinical Trials

A Phase 1 Study of TDM-180935 Following Topical Administration in Healthy Male Subjects

Start date: February 8, 2023
Phase: Phase 1
Study type: Interventional

Multi-center, randomized, double-blind, vehicle-controlled, parallel group, dose escalation study of TDM-180935 following topical administration in healthy male subjects, 18 to 55 years old

NCT ID: NCT05525403 Completed - Healthy Clinical Trials

The Effects of Fatigue on Exercise-Induced Hypoalgesia During a Dynamic Resistance Exercise

Start date: October 28, 2022
Phase: N/A
Study type: Interventional

The primary purpose of this study is to compare immediate changes in pain sensitivity (pressure pain threshold) during quiet rest, low fatigue exercise, and high fatigue exercise.

NCT ID: NCT05524636 Completed - Healthy Clinical Trials

Effects of Peripheral Magnetic Stimulation

Start date: July 15, 2022
Phase: N/A
Study type: Interventional

Interventional study of the effectiveness of peripheral magnetic stimulation of the abdominal wall muscles in healthy individuals.

NCT ID: NCT05523401 Recruiting - Healthy Clinical Trials

Acute Effects of 2C-B Compared With MDMA and Psilocybin in Healthy Subjects

2C-B
Start date: August 16, 2023
Phase: Phase 1
Study type: Interventional

4-bromo-2,5-dimethoxyphenethylamine (2C-B) is a psychoactive substance with reportedly similar acute effects to both the prototypical empathogen 3,4-methylenedioxymethamphetamine (MDMA, Ecstasy) and the classic psychedelic substance psilocybin (contained in "magic, hallucinogenic mushrooms"). Pharmacologically, MDMA mainly releases serotonin (5-HT) via the serotonin transporter (SERT) and psilocybin mainly acts as direct agonist at 5-HT2A receptors. 2C-B interacts with both the 5-HT2A receptor and SERT which is in line with its reported mixed effects profile. However, scientific studies are lacking. There is an increased interest in psychiatric research on the therapeutic properties of MDMA and psilocybin and also on mixed empathogenic-psychedelic substances.

NCT ID: NCT05522777 Completed - Healthy Clinical Trials

Survival of the Probiotic Lacticaseibacillus Paracasei Strain Shirota (LcS) in the GI Tract of Healthy Adults

Start date: August 15, 2022
Phase: N/A
Study type: Interventional

The objective of this study is to investigate the survival of Lacticaseibacillus paracasei strain Shirota (LcS) in the human gastrointestinal (GI) tract after consumption of probiotics fermented milk product containing 8x10^9 LcS. This study is a single-arm, open-label study with a 14-d run-in (baseline), 14-d consumption period, and 14-d follow-up. Participants will maintain habitual dietary and lifestyle practices with the exception of avoiding fermented foods and beverages throughout the 42-d trial. The number of live LcS in fecal samples will be assessed after 14 d consumption of a fermented milk product.