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Aging clinical trials

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NCT ID: NCT00427193 Completed - Aging Clinical Trials

CALERIE: Comprehensive Assessment of Long-Term Effects of Reducing Intake of Energy

Start date: May 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to test the hypothesis that two years of sustained 25% caloric restriction (CR) in men age 21-50 (inclusive) and women age 21-47 (inclusive) will slow aging and protect against age-related disease processes.

NCT ID: NCT00400062 Completed - Aging Clinical Trials

MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care

Start date: July 1, 2007
Phase:
Study type: Observational

This will be the first large cohort study to define the epidemiology of and identify modifiable risk factors for long-term CI and functional deficits of ICU survivors. The investigators will measure the independent contribution of risk factors such as delirium and exposure to sedative and analgesic medications to the incidence of long-term CI, controlling for established risk factors (e.g., age, pre-existing CI, and apoE genotype). Defining the contributions of these risk factors will make it possible to develop preventive and/or treatment strategies to reduce the incidence, severity and/or duration of long-term CI and improve functional recovery of patients with acute critical illness.

NCT ID: NCT00395837 Completed - Aging Clinical Trials

Efficacy of Lifestyle Changes in Modifying Practical Markers of Wellness and Aging.

Start date: September 2004
Phase: N/A
Study type: Interventional

To assess the impact of lifestylel changes upon measures of wellness and aging, in particular weight change, fitness measures, and cognitive performance. The hypothesis was that aerobic exercise would improve mental performance and measures of fitness.

NCT ID: NCT00383357 Completed - Aging Clinical Trials

Sleepiness and the Risk of Falling

Start date: August 2004
Phase: N/A
Study type: Interventional

The purpose of this project is to examine the impact of sleeping pills and waking up in the middle of the night on walking balance and cognitive function, to identify risk factors for falls in older adults. A significant percentage of falls, approximately 33 to 52 percent, occur during the nighttime and morning hours when people are normally sleeping; therefore, it is possible that sleep and sleeping medication related impairments in balance may contribute to this risk.

NCT ID: NCT00380562 Completed - Aging Clinical Trials

The Baltimore Experience Corps Study

Start date: July 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effectiveness of the Experience Corps program in preventing or delaying physical disability in older adults, by studying the effects of volunteerism on physical, social and cognitive well-being.

NCT ID: NCT00365794 Completed - Obesity Clinical Trials

Effects of Testosterone Gel on Carbohydrate and Lipid Metabolism In Elderly Obese Men

Start date: August 2006
Phase: Phase 2
Study type: Interventional

A. HYPOTHESES: In older men low testosterone levels, abdominal obesity and elevated fasting insulin who are at risk for the cardiovascular complications such as heart attack and stroke. 1. Supplemental testosterone will decrease abdominal adipose tissue and hepatic fat) and appendicular fat and intramyocellular lipid in peripheral muscles (IMCL). 2. Supplemental testosterone will improve insulin sensitivity by: 1. Decreasing hepatic glucose output (HGO), a measure of central insulin resistance 2. increasing peipheral glucose disposal (Rd), a measure of periperal insuln sensiivity 3. . Improving peripheral glucose disposal (Rd) by reducing IMCL 4. Increasing appendicular skeletal muscle mass B. OBJECTIVES: 1. Primary Objective: To determine the effects of supplemental testosterone to achieve testosterone levels in the upper normal physiologic range on central adipose tissue (abdominal and hepatic fat) and peripheral skeletal muscle fat (appendicular fat and IMCL). 2. Secondary Objectives: To determine the effects of supplemental testosterone to achieve testosterone levels in the upper normal physiologic range:on central insulin sensitivity ( hepatic glucose output ([HGO]) and peripheral insulin sensitivity (glucose disposal (Rd) Results of this study will provide greater understanding whether androgen therapy enhances insulin sensitivity by decreasing HGO, improving peripheral Rd and if these desired effects are achieved, whether they are due to reductions in abdominal fat or liver lipid, IMCL or effects of augmenting muscle mass per se. Results will generate hypotheses to investigate cellular and molecular mechanisms of androgen effects in persons at risk for the Metabolic Syndrome.

NCT ID: NCT00337974 Completed - Aging Clinical Trials

Computer-Based Training for Cognitive Enhancement: In Home Study

Start date: March 2005
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the effects of a computer-based training program on the memory and cognitive abilities of mature individuals undergoing healthy aging.

NCT ID: NCT00337909 Completed - Aging Clinical Trials

Computer-Based Training for Cognitive Enhancement: Classroom Study

Start date: September 2005
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the design and effectiveness of a computer-based training program on the memory and cognitive abilities of mature individuals undergoing healthy aging.

NCT ID: NCT00336232 Completed - Aging Clinical Trials

Determinants of Vitamin K Metabolism

Start date: May 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to learn how the body responds to different amounts of vitamin K in the diet in order to understand the roles that vitamin K may have in the body. We also need to determine if older adults need more or less vitamin K in their diet compared to younger adults in order to maintain normal body stores of vitamin K.

NCT ID: NCT00328055 Completed - Aging Clinical Trials

Comparison of an Easy to Read Advance Directive Versus a Standard Advance Directive

Start date: August 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the acceptability, usefulness, self-efficacy and comprehension of an easy-to-read advance directive form versus a standard advance directive form written at a post graduate reading level.