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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06363409
Other study ID # 2023-1353
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2024
Est. completion date January 1, 2027

Study information

Verified date April 2024
Source San Diego State University
Contact Mark Kern, PhD, RD
Phone 619-594-1834
Email kern@sdsu.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the research is two-fold. One goal is to determine if post-exercise almond or cereal bar consumption can promote muscle gain as well as increasing muscular strength throughout an eight-week weight training program. The other goal is to assess the short-term effects of almonds or cereal bar on recovery that may explain the overall long-term adaptations.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date January 1, 2027
Est. primary completion date June 1, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - BMIs of 18.5-30 kg/m2 - participate in no more than 3 hours of structured exercise per week Exclusion Criteria: - weight training more than 30 min/week, - smoking, - use of medications known to impact inflammation, - musculoskeletal limitations, - use of supplements within 1 month of participation that are known to impact body composition, antioxidant or inflammatory status, - regular consumption of more than 2 servings of nuts per week, - unwillingness to refrain from recovery treatments during the study such as hydrotherapy, massage, stretching, compression garments, anti-inflammatory medications and topical applications.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cereal Bar as a recovery food snack
Cereal bar as a recovery snack food
Almond
Almond as a recovery snack food

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
San Diego State University

Outcome

Type Measure Description Time frame Safety issue
Primary delayed onset of muscle soreness measuring delayed onset of muscle soreness using visual analogue scale (VAS) baseline, 24 hour, 48 hour, and 72 hour after baseline
Primary markers of muscle damage Blood markers of muscle damage (creatine kinase (u/L)) Baseline, 24 hour, 48 hour and 72 hour after baseline
Primary changes in strength muscle cross-sectional area of the calf via peripheral quantitative computerized tomography (pQCT) Baseline and 8 weeks
Primary changes in body composition measuring body composition by dual energy x-ray absorptiometry (DXA) Baseline and 8 weeks
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