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Sarcopenia clinical trials

View clinical trials related to Sarcopenia.

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NCT ID: NCT02103842 Completed - Sarcopenia Clinical Trials

Omega-3 Fatty Acids to Combat Sarcopenia

Start date: March 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine how omega-3 fatty acids influence muscle protein metabolism and mitochondrial physiology in the context of human aging.

NCT ID: NCT02089971 Completed - Sarcopenia Clinical Trials

Muscle Mass and Function in Chinese Adults

Start date: March 2014
Phase: N/A
Study type: Observational

To describe the normal range of muscle mass and function in Chinese adults.

NCT ID: NCT02089906 Completed - Sarcopenia Clinical Trials

Health and Nutrition Status of Chinese Elderly

Start date: March 2014
Phase: N/A
Study type: Observational

This study is aiming to understand the prevalence and risk factors related to malnutrition and sarcopenia in Chinese elderly.

NCT ID: NCT02069314 Completed - Sarcopenia Clinical Trials

Diet and Muscle Function In Older Adults

S32
Start date: May 2012
Phase: N/A
Study type: Interventional

This research study was conducted to investigate the effects of a high protein diet on the efficiency of energy use at rest and at low-levels of physical activity. The hypothesis was that a high intake of dietary protein would result in a less efficient use of energy in skeletal muscle in older adults.

NCT ID: NCT02062086 Completed - Sarcopenia Clinical Trials

Estimation of Muscle Mass in Older Adults Using Deuterated Creatine

MM-DC
Start date: June 2014
Phase: N/A
Study type: Interventional

Current methods for the quantification of muscle mass are indirect, lack precision, and often rely on expensive equipment that only provides limited (indirect) data on whole body muscle mass. Dual energy X ray absorptiometry has emerged as a potential precise measure of lean mass, easy to use in clinical practice and research. However, it assesses an indirect measurement of total-body skeletal muscle mass and its clinical use for determination of changes in muscle mass may be very limited due to instrumentation availability, particularly in field studies, and cost. Moreover, these methods provide estimates of fat free mass that is not skeletal muscle specific, and are influenced by changes in regional or total body water content. GlaxoSmithKline (GSK) has developed a novel technique using deuterium labeled creatine dilution for the estimation of muscle mass and has begun clinical evaluation of this muscle-measure in healthy young and older adults.

NCT ID: NCT02053441 Completed - Sarcopenia Clinical Trials

Modulation of Muscle Protein Synthesis With Diet and Exercise in Old Aged Women

Start date: January 2013
Phase:
Study type: Observational

In this study will measure differences in how muscle responds to both exercise and protein supplements in healthy women aged 60-69. We are studying two different protein supplements- a standard Whey Protein and a Leucine enriched supplement. Each patient would receive either one of these.

NCT ID: NCT02047864 Completed - Osteoporosis Clinical Trials

Effect of Creatine Supplementation and Exercise on Bone Health

Start date: January 2014
Phase: N/A
Study type: Interventional

Osteoporosis is an important health problem, costing the Canadian health care system over $2 billion per year. Loss of bone mineral and bone fragility is especially prevalent in postmenopausal women. Of all osteoporotic fractures, hip fractures are the most traumatic. Creatine monohydrate is a nutritional supplement that is often combined with strength training to increase strength and muscle mass. The investigators recently completed a pilot study in a small number of postmenopausal women (n=33) that showed that creatine monohydrate significantly improved hip bone mineral density during a 1-year resistance training program. In our current proposal the investigators want to determine whether creatine combined with strength training can have an even larger effect on bone mineral density at the hip if given over 2 years in a large group of postmenopausal women (n=240). The investigators also want to determine whether this leads to reduced fractures in these women for up to a year after completing the creatine and strength training program.

NCT ID: NCT02043171 Completed - Sarcopenia Clinical Trials

Nutritional Intervention for Age-related Muscular Function and Strength Losses-Study 2

Start date: August 2014
Phase: Phase 1
Study type: Interventional

Men and women lose muscle mass and strength with age. Loss of muscle mass and strength is accompanied by a loss of muscle function which can lead to diminished quality of life and more importantly can lead to serious fall requiring medical treatment. The investigators hypothesize that the combined supplements of Calcium-HMB and Vitamin D will lead to decreased falls and to improved quality of life (QOL) for older adults. The investigators further hypothesize that the addition of a modest exercise regimen to these supplements will enhance the synergistic effects of both Calcium-HMB and Vitamin D. Subjects will consume the dietary supplement 2 times per day for 12 months. Tests will consist of the following: a) strength of subjects' legs and elbow by Isokinetic Dynamometer; b) body composition; c) hand-grip strength by hand-grip dynamometer; d) functional mobility, balance and agility (Get-Up and Get-Up-and-Go tests); e) filling out questionnaires; and g) having blood drawn for biochemical measurements. Testing will be performed at the baseline (0 months) and at 3, 6, 9, and 12 months.

NCT ID: NCT02034760 Completed - Sarcopenia Clinical Trials

Counteracting Age-related Loss of Skeletal Muscle Mass

CALM
Start date: January 10, 2014
Phase: N/A
Study type: Interventional

Up to approximately 205 (dependent on drop-out rate) healthy elderly individuals (at least 65 years old) are recruited as subjects. Upon inclusion, each individual will be randomized into one of the five groups stratified according to gender (M/F) and 30s chair stand (<16 OR ≥16). The five groups are: Heavy Resistance Training (N=30-35), Light Intensity Training (N=30-35), Protein Whey (N=40-50), Protein Collagen (N=40-50) and Carbohydrate (N=30-35). The individuals randomized into one of the supplementation groups (Protein Whey, Protein Collagen or Carbohydrate) will be blinded to the supplement content. Assessments will be performed at Baseline (before intervention start), and after 6 and 12 months of intervention and again at 18 months (after 6 months of follow up). The primary outcome is change in quadriceps muscle cross sectional area from Baseline to 12 months of intervention. The primary hypothesis is that by applying the intension-to-treat analysis, the Light Intensity Training group will increase quadriceps muscle cross sectional area just as much as the Heavy Resistance Training group. The two training groups will gain more muscle mass than the Protein Whey group, which will gain more than the Protein Collagen and the Carbohydrate groups that will loose quadriceps muscle cross sectional areas.

NCT ID: NCT02013466 Completed - Sarcopenia Clinical Trials

Amino Acid Bioavailability in Healthy Elderly After Intake of an Oral Nutritional Supplement

ArenA
Start date: October 2008
Phase: Phase 1
Study type: Interventional

In this study healthy older adults are requested to consume 4 different high-protein nutritional supplements. Each subject will visit the site 4 times and at every visit they will consume 1 of the 4 products after which a series of blood samples will be taken. The blood samples will be analyzed for amino acid bioavailability in the blood up to 4 hours after consumption.