| Registry | NCT04371237 |
|---|---|
| Status | Completed |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: none, basic science |
| Enrollment | 26 (Actual) |
| Sponsor | PepsiCo Global R&D (Industry) |
| Conditions | Muscle Recovery, Muscle Soreness, Glycogen Depletion |
| Interventions | Compression sleeve, Heat therapy, Glycogen-depleting exercise session, Nutrient Intake (beverage), Skeletal muscle biopsy (Device, other, procedure) |
| Dates | start 2018-09-19, primary completion 2019-12-21, completion 2019-12-21, first posted 2020-05-01, last updated 2021-03-10 |
| Locations | 1 site in United States |
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To determine if modalities designed to improve blood flow combined with post-exercise nutrient intake will improve replenishment of muscle glycogen better than nutrient intake alone. A secondary objective is to compare the effectiveness of heat therapy and intermittent pneumatic compression on glycogen replenishment.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Intermittent pneumatic compression | Experimental | Device: Compression sleeve; Other: Glycogen-depleting exercise session; Other: Nutrient Intake (beverage); Procedure: Skeletal muscle biopsy | IPC sleeve device on leg |
| Heat therapy | Experimental | Device: Heat therapy; Other: Glycogen-depleting exercise session; Other: Nutrient Intake (beverage); Procedure: Skeletal muscle biopsy | Custom water-circulating garment on leg |
Sex: All, ages: 18 Years to 35 Years, accepts healthy volunteers
Inclusion Criteria: 1. Subjects will be male and female participants in good health 2. 18-35 years of age 3. Currently performing cardiovascular or intermittent exercise at a moderate to high intensity at least 5 days per week for 60 minutes or longer per day. 4. Understanding of the procedures to be undertaken as part of the study 5. Willingness to participate in exercise testing and follow instructions provided by the experimenter 6. Informed, voluntary, written consent to participate in the study Exclusion Criteria: 1. History of deep vein thrombosis 2. Obesity (BMI > 30 kg/m2) 3. Hypertension (resting SBP > 140/90 mmHg) 4. Smoking 5. Pregnant, planning to become pregnant, or lactating 6. Supplements containing antioxidants including vitamin C and E and N-acetyl cysteine 7. Any medication 8. Lactose intolerance 9. Participation in another study within the previous 30 days or in a PepsiCo funded study within the past 6 months.
| Facility | City | Country | Status |
|---|---|---|---|
| Purdue University, Department of Health & Kinesiology | West Lafayette, Indiana | United States |