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Blood flow restriction training for Healthy Subjects
N/A
Waitlist Available
Research Sponsored by University of South Carolina
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 baseline, week 3, and week 6
Awards & highlights
Study Summary
This trial is testing whether a minimal equipment training program with or without blood flow restriction training is more effective than traditional concurrent resistance and endurance training in improving Army Combat Fitness Test performance, laboratory measures of performance, and tendon architecture.
Eligible Conditions
- Healthy Subjects
- Military Operations
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, week 3, and week 6
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, week 3, and week 6
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Army Combat Fitness Test
Secondary outcome measures
Change in aerobic capacity
Body Weight Changes
Change in blood-based biomarkers
+6 moreTrial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: Minimal equipment resistance and endurance training with blood flow restrictionExperimental Treatment2 Interventions
Participants in this group undergo 6 weeks of concurrent resistance and endurance training using minimal equipment (i.e., sandbags, resistance bands, suspension trainers, weight vests, etc.) while wearing upper- and lower-body blood-flow restriction cuffs
Group II: Minimal equipment resistance and endurance trainingExperimental Treatment1 Intervention
Participants in this group undergo 6 weeks of concurrent resistance and endurance training using minimal equipment (i.e., sandbags, resistance bands, suspension trainers, weight vests, etc.)
Group III: Traditional equipment resistance and endurance trainingActive Control1 Intervention
Participants in this group undergo 6 weeks of concurrent resistance and endurance training using traditional equipment (i.e., power racks, barbells, dumbbells, etc.)
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Who is running the clinical trial?
United States Department of DefenseFED
859 Previous Clinical Trials
225,444 Total Patients Enrolled
University of South CarolinaLead Sponsor
210 Previous Clinical Trials
120,375 Total Patients Enrolled
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