Efficacy of Lifestyle Changes in Modifying Practical Markers of Wellness and Aging.
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|ClinicalTrials.gov Identifier: NCT00395837|
Recruitment Status : Completed
First Posted : November 3, 2006
Last Update Posted : November 3, 2006
|Condition or disease||Intervention/treatment||Phase|
|Aging||Behavioral: Aerobic exercise||Not Applicable|
A 10-week, randomized control study conducted in a wellness center in St. Petersburg, Florida. Adults age 21-65, exercising less than 3 days/week. 56 subjects were randomized to a control or an intervention group. Subjects followed a diet with >30 grams of fiber and <16 grams of saturated fat daily, and were taught to reach 70-85% of their maximum heart rate 5-6 days/week, and to perform strength training 3 days/week, plus were asked to participate in 10-20 minutes of stress management activities daily. The study was designed to determine body composition, maximal aerobic capacity (VO2 max), total cholesterol/high-density lipoprotein (TC/HDL), and cognition.
Specific aspects ofcognitive performance were noted to increase with increasing levels of aerobic activity, but not with strength training, dietary fiber change, or stress managment.
Having established that the treatment group would exercise at different levels of intensity, additional subjects were recruited, and the cognitive performance of no exercise, moderate aerobic exercise, and frequent aerobic exercise could be compared with specific domains of cognitive performance: memory, psychomotor speed, reaction time, attention, and cognitive flexibility. The St Anthony’s Institutional Review Board approved this research project.
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||56 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Efficacy of Lifestyle Changes in Modifying Practical Markers of Wellness and Aging|
|Study Start Date :||September 2004|
|Study Completion Date :||May 2006|
- Cognitive performance (memory, psychomotor speed, reaction time, attention, cognitive flexibility)
- Cholesterol profile
- Weight change
- Body fat change
- Changes in fitness (strength, flexibility, VO2max)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00395837
|United States, Florida|
|Carillon Wellness Center|
|St Petersburg, Florida, United States, 33716|
|Principal Investigator:||Steven C Masley||Medical Director|