- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06363409
The Acute and Accumulative Effects of Snack Foods on Exercise Recovery
April 9, 2024 updated by: San Diego State University
The Acute and Accumulative Effects of Almonds on Exercise Recovery
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.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Mark Kern, PhD, RD
- Phone Number: 619-594-1834
- Email: kern@sdsu.edu
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Cereal bar arm
weight lifting exercise and post-exercise cereal bar consumption
|
Cereal bar as a recovery snack food
|
Experimental: Almond arm
weight lifting exercise and post-exercise almond consumption
|
Almond as a recovery snack food
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
delayed onset of muscle soreness
Time Frame: baseline, 24 hour, 48 hour, and 72 hour after baseline
|
measuring delayed onset of muscle soreness using visual analogue scale (VAS)
|
baseline, 24 hour, 48 hour, and 72 hour after baseline
|
markers of muscle damage
Time Frame: Baseline, 24 hour, 48 hour and 72 hour after baseline
|
Blood markers of muscle damage (creatine kinase (u/L))
|
Baseline, 24 hour, 48 hour and 72 hour after baseline
|
changes in strength
Time Frame: Baseline and 8 weeks
|
muscle cross-sectional area of the calf via peripheral quantitative computerized tomography (pQCT)
|
Baseline and 8 weeks
|
changes in body composition
Time Frame: Baseline and 8 weeks
|
measuring body composition by dual energy x-ray absorptiometry (DXA)
|
Baseline and 8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mark Kern, PhD, RD, San Diego State University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 1, 2024
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
January 1, 2027
Study Registration Dates
First Submitted
April 2, 2024
First Submitted That Met QC Criteria
April 9, 2024
First Posted (Actual)
April 12, 2024
Study Record Updates
Last Update Posted (Actual)
April 12, 2024
Last Update Submitted That Met QC Criteria
April 9, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2023-1353
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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