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Energy Deficit for Energy Deficiency Syndrome
N/A
Waitlist Available
Research Sponsored by United States Army Research Institute of Environmental Medicine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 days
Awards & highlights
No Placebo-Only Group
Summary
This trialexamines how energy balance & energy deficit affects protein & carb oxidation when consuming protein & exercising. It tests effects in healthy adults.
Eligible Conditions
- Stress
- Energy Deficiency Syndrome
- Energy Deficiency
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Carbohydrate Oxidation during Steady-state Exercise
Muscle Protein Synthesis
Whole-body protein balance
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Group I: 60% Energy DeficitExperimental Treatment1 Intervention
Energy Deficit equal to 60% total daily energy requirements.
Group II: 40% Energy DeficitExperimental Treatment1 Intervention
Energy Deficit equal to 40% total daily energy requirements.
Group III: 20% Energy DeficitExperimental Treatment1 Intervention
Energy Deficit equal to 20% total daily energy requirements.
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Who is running the clinical trial?
United States Army Research Institute of Environmental MedicineLead Sponsor
64 Previous Clinical Trials
3,589 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have conditions like kidney disease, diabetes, or heart problems that affect your metabolism, heart, or digestion.You have been regularly doing aerobic or strength exercises for at least 2 days a week for the past 6 months, based on your self-report.You have had problems or complications when using lidocaine in the past.Your body weight is within a healthy range for your height.
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Research Study Groups:
This trial has the following groups:- Group 1: 20% Energy Deficit
- Group 2: 40% Energy Deficit
- Group 3: 60% Energy Deficit