The Pacing (Guided Vs Unguided) Strategies Study
Completed · Not applicable
Conditions studied: Body Temperature Changes
In brief
The objectives of this study are to demonstrate that real time physiological status monitoring and the use of optimization techniques during exercise can have a positive impact on physiological status, and to collect metabolic flexibility profiles of young fit adults during rest and exercise.
Key facts
- Study ID
- NCT02310334
- Run by
- USDA Beltsville Human Nutrition Research Center
- People needed
- 23
- Starts
- 2014-08-01
- Expected to finish
- 2015-12-01
- Last updated by the study team
- 2016-02-24
Who can join
Age: 18 and older, up to 29. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Male and Female
- Ages 18 to 29 at the beginning of the study
- Relatively fit can run 2 miles in under 16 minutes
You may not qualify if…
- History of Skin Sensitivity to Nickel
- Hypertension
- Alcoholism
- Diabetes
- Pregnant
- Age >29
- Cannot run 2 miles in less than 16 minutes
- No regular weekly exercise
- Difficulty Swallowing Food or Large Pills
- Diverticulitis
- Inflammatory Bowel Disease
- Peptic Ulcer Disease
- Crohn's Disease
- Ulcerative Colitis
- Previous Gastrointestinal Surgery
- Possible Nuclear Magnetic Resonance Scan
- Women who have given birth during the previous 12 months
- Pregnant women or women who plan to become pregnant or become pregnant during the study
- Lactating women
- History or presence of kidney disease, liver disease, certain cancers, gastrointestinal, pancreatic, other metabolic diseases, or malabsorption syndromes
- History of bariatric or certain other surgeries related to weight control
- Smokers or other tobacco users (for at least 6 months prior to the start of the study)
- History of eating disorders or other dietary patterns which are not consistent with the dietary intervention (e.g., vegetarians, very low fat diets, high protein diets)
- Volunteers who have lost 10% of body weight within the last 12 months or who plan to initiate a weight loss program during the next 10 months
- Unable or unwilling to give informed consent or communicate with study staff.
Where it is running
- Beltsville Human Nutrition Research Center — Beltsville, Maryland, United States
Full record on ClinicalTrials.gov
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