Clinical Trials Logo

Healthy clinical trials

View clinical trials related to Healthy.

Filter by:

NCT ID: NCT01080378 Not yet recruiting - Healthy Clinical Trials

Metabolic Effects of Birth Weight on Overweight and Obese Chinese Adults and Their Responses to Weight Loss

SAMS-2
Start date: April 2010
Phase: N/A
Study type: Interventional

The overall objective of this study is to investigate in depth the impact of birth weight on the nature of metabolic physiology, body composition and epigenetic differences of the different phenotypes of overweight and obese individuals who are otherwise overtly healthy. We also aim to determine the efficacy of a weight loss intervention on the above mentioned metabolic parameters in these individuals.

NCT ID: NCT01066975 Not yet recruiting - Healthy Clinical Trials

Mechanical Load on the Shoulders While Carrying a Backpack- Towards a Knowledge-Based Backpack Design

Start date: February 2010
Phase: N/A
Study type: Observational

Soldiers and recreational backpackers are often required to carry heavy loads on their body during military operations or hiking. Despite the advances in backpack design, the loads carried by soldiers still impose an extreme physiological strain (soft tissue deformation) which frequently results in discomfort, pain,musculoskeletal injuries, and loss sensorimotor function. In the current study, characterization of the pressures, evaluation of the deformations of the soft tissues, specifically the fat, muscles, Brachial plexus and subclavian vessels applied on the shoulder while sitting with a heavy backpack will performed. The data acquired in the current trials will be used for development of a finite element (FE) 3D shoulder model. The purpose is to better understand the mechanical loads that are being transferred to the underlying tissue below the shoulder straps during walking/marching with a backpack. During the 2nd phase of this project, data collected during this research will be used to develop gear that will alleviate the strain on the shoulders, prevent injury, and enhance performance. Hypothesis - High focal strain (hot-spots) on the shoulder tissue that are observed with the pressure mapping will be observed also in the MR scans. - The strain at those hot-spots can be reduced by personal-geometry adjusted straps. Volunteers Five young (18-30 yrs), healthy, and fit males will participate in this study. Trials design 1. MR Scans- The scan will be performed for analysis of personal shoulder anatomy, and will be used for developing a 3D FE model. The sagittal view will be used to develop the 3D model. The coronal and axial sectional views will be used to assess the deformations applied on the shoulder tissue. The scan will then be repeated while carrying a 25 kg standard commercial backpack while sitting in the same position, for the assessment of shoulder girdle tissues deformations. Time estimation for each scan is 40 min (80 min total). The subjects are not required to carry the backpack prior to those scans. 2. Static pressure measurement- each volunteer will be asked to sit for 30 seconds while carrying the 25 kg backpack. During this session, pressure will be measured using a pressure mapping pad (Sensor Products Inc., USA) placed between the shoulder strap and the underlying tissue. The maximal total participation time of each volunteer will be 2 hours total (inside and outside the MR). Data acquired in the current trials will be used for the development of a FE (finite element) 3D shoulder model. MR scans will be utilized for composing geometry and for the boundary conditions assessment (strain magnitude). Pressure measurements will be used as boundary conditions (stress magnitude). MR scans and pressure measurements will be performed in the Sheba medical center facilities.

NCT ID: NCT01039623 Not yet recruiting - Healthy Clinical Trials

Assessment of Safety and Immunogenicity of Intradermal Unadjuvanted Portion of Pandemrix® Via a Microneedle Device With Intramuscular Adjuvanted Pandemrix® as Reference

Start date: January 2010
Phase: N/A
Study type: Interventional

Healthy volunteers will be vaccinated against H1N1 pandemic influenza. One group will receive the adjuvant vaccine while the other group will get intradermal antigen, without the adjuvant. The antibody production will be compared.

NCT ID: NCT01003171 Not yet recruiting - Healthy Clinical Trials

Pharmacokinetics of MCS in Healthy Volunteers

MCS-2-US-pk
Start date: August 2011
Phase: Phase 1
Study type: Interventional

This study is to examine the pharmacokinetics, absorption and serum concentrations of MCS and other components after once-daily oral dosing of MCS.

NCT ID: NCT01003041 Not yet recruiting - Healthy Clinical Trials

The Influence of Hearing Discrete Phonemes in Mother's Voice in the Infant's Natural Environment and With Natural Melody on Developing Phonetic Categories Between 4-10 Months Old

Start date: October 2009
Phase: N/A
Study type: Observational

The purpose of this study is to record voice samples of infant's mothers, process in samples to a phonetic musical piece, play the phonetic musical piece to 4-10 month old infants, and then test the infants in a conditioned head turning test in lab, and to analyze the results.

NCT ID: NCT00894881 Not yet recruiting - Healthy Clinical Trials

The Effect of Colonoscopy on Resting Energy Expenditure

Start date: May 2009
Phase: N/A
Study type: Observational

The Effect of Gut Cleaning as a Preparation to Colonoscopy on resting energy expenditure (REE).

NCT ID: NCT00815841 Not yet recruiting - Healthy Clinical Trials

Methylphenidate in Healthy Young Adults

Start date: January 2009
Phase: Phase 4
Study type: Interventional

Background: There is a paucity of data as to the effect of methylphenidate (MPH) on young adults who do not have attention deficit hyperactivity disorder (ADHD). The existing data is equivocal and focuses on neuropsychological functions that are not always relevant to the clinical aspects of attention. Objective: To determine the effect of MPH on a diagnostic continuous performance task that assesses attention per se (TOVA) and on a decision making test (Modified Gamble Decision Test) in young, healthy adults. Methods: Fifty young adults, men and women ages 20-30, without ADHD, learning disabilities, history of past or present use of MPH or other psychotropic drugs, will be eligible to participate. Design: The experiment will be conducted in 2 sessions, the first lasting 3.5 hours and the second 2.5 hours in a randomized, double-blind prospective design. In the first session, the subjects will be screened for ADHD past and present, major psychiatric diagnosis (depression, anxiety, etc), use of MPH in the past, psychotropic medications or recreational drugs and any other chronic illness; urine will be tested for beta-hCG to rule out pregnancy. Blood pressure and heart rate will be measured. The participants will then be given either placebo or MPH (15-20 mg) and after 90 minutes will proceed to complete the TOVA (that lasts 22 minutes) and Modified Gamble-Decision Test (15 minutes). Before taking the pill and prior to the testing, the subjects will complete the Visual Analogue Scale (VAS) which quantifies their subjective feelings regarding present mental and emotional state. In the second session, 2 weeks later, blood pressure and heart will be measured and the VAS completed prior to and 90 minutes after taking the tablet. The subjects then undergo the TOVA and Modified Gamble-Decision Test. Data Analysis: will be performed using the paired t-tests for parametric variables and one way ANOVA with repeated measurements. Significance: Results of this study are important since MPH is used and abused by healthy students as a "study aid" although its objective effects in normal young adults are not well delineated

NCT ID: NCT00729820 Not yet recruiting - Healthy Clinical Trials

The Influence of Personality on Two Aspects of Cognitive Performance: Processing Speed, and Accuracy.

Start date: August 2008
Phase: N/A
Study type: Observational

Recently, a lot of evidence for a relation between measures of cognitive performance and personality characteristics has been collected. The use of computer based latency measures is often used to study mental processes in cognitive, as well as, in personality research On the basis of these relationships we can ask a question that relates to the practical usefulness (validity) of processing speed, accuracy of performance and personality measures in predicting impulsive behavior.

NCT ID: NCT00689494 Not yet recruiting - Healthy Clinical Trials

Cervical Device Contraception-2 (Nanopaz)

NANOPAZ
Start date: June 2008
Phase: Phase 1/Phase 2
Study type: Interventional

Measure blood progesterone by using cervical device contraception.

NCT ID: NCT00660465 Not yet recruiting - Healthy Clinical Trials

Exploring the Relationship Between Varying CO2 Levels and the Regional BOLD Signal, by Using Breathing Exercises

Start date: May 2008
Phase: N/A
Study type: Observational

The purpose of this study is to explore how arterial PaCO2 effect regional Blood Oxygen Level Dependent (BOLD) signal, and indirectly the brain regional O2 level .