- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06172543
The Effects of Nutritional Supplementation on Occupational Performance in Firefighters
The Effects of Protein and Carbohydrate Supplementation, With and Without Creatine, on Occupational Performance in Firefighters
The purpose of this study was to assess the usefulness of protein and carbohydrate supplementation, with and without creatine, on occupational performance in firefighters. Research has examined the effects of adding creatine to whey protein and carbohydrates on training adaptations in resistance-trained individuals with mixed finding.
Furthermore, the ergogenic benefit of protein and carbohydrate supplementation, with or without creatine, in firefighters is largely unknown. Therefore, the primary aim of the current study was to examine the effects of protein and carbohydrate supplementation, with or without creatine, on occupational performance in firefighters.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Wisconsin
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La Crosse, Wisconsin, United States, 54601
- Fire Department
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being a firefighter between the ages of 18-55 years of age, and medically cleared for field duty.
Exclusion Criteria:
- Any current musculoskeletal or neurological condition that would prohibit the completion of performance testing.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Creatine Monohydrate Group
25 grams of Whey Protein Isolate + 25 grams of Carbohydrate Powder + 5 grams of Creatine
|
Participants were assigned to ingest a single serving daily of either A) a 25-gram dose of whey protein isolate + 25-gram dose of carbohydrate powder (ProCarb); or B) a 25-gram dose of Whey Protein Isolate + 25-gram dose of carbohydrate powder + 5-gram dose of creatine monohydrate (Creatine) for a 17-21-day period.
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Placebo Comparator: Non Creatine Group
25 grams of Whey Protein Isolate + 25 grams of Carbohydrate Powder only
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A 25-gram dose of whey protein isolate + 25-gram dose of carbohydrate powder (ProCarb)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time to completion
Time Frame: 24 Days
|
Time to completion for tasks including a hose carry, body drag, stair climb, and forcible entry (Keiser sled hammer) for time.
For the hose carry, firefighters advanced a 30.48 m section of a charged 4.45 cm hose line over a distance of 30.5 m in a straight line before flowing water for 2 seconds.
Rescue consisted of firefighters being instructed to grasp a mannequin (mass 50 kg, height: 180 cm) underneath the shoulders using a "seatbelt" grip and dragging the mannequin 30.5 m backward.
This test is known as the body drag.
Stair climb consisted of climbing four flights of stairs and returning to the bottom as quickly as possible.
In the forcible entry, firefighters struck a simulated forcible entry chopping device (Keiser FORCE Machine, Keiser Co., USA) using a 3.6 kg sledgehammer until completed.
The total time to complete each task was recorded, in addition to the total completion time for all tasks summed together.
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24 Days
|
Time Trial
Time Frame: 24 Days
|
A maximal effort, 3.5 km time trial on an air-braked cycle ergometer (Assault Bike, As-sault Fitness Products, Carlsbad, CA, USA).
|
24 Days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Andrew Jagim, PhD, Mayo Clinic
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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