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

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.

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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