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CompletedNCT06172543Updated Dec 15, 2023

The Effects of Nutritional Supplementation on Occupational Performance in Firefighters

An interventional study of Creatine Monohydrate and Control in Fatigue, sponsored by Ward Dobbs. Completed at 1 site in United States. Open to male participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-12-15.

Sponsored by Ward Dobbs · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Mar 2023, registered Nov 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
Male
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Study summary

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.

02

Conditions studied

  • Fatigue

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Keywords

  • Creatine
03

In context

Fatigue

1,860 studies on the registry are indexed under Fatigue; 376 are open to participants now.

This study's enrollment of 30 is below the median of 54 across 1,440 interventional studies indexed under Fatigue.

Browse Fatigue studies →

Lead sponsor

This is the only study on the registry with Ward Dobbs as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Being a firefighter between the ages of 18-55 years of age, and medically cleared for field duty.

Exclusion criteria

Exclusion Criteria:

  • Any current musculoskeletal or neurological condition that would prohibit the completion of performance testing.
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Creatine Monohydrate Group

    25 grams of Whey Protein Isolate + 25 grams of Carbohydrate Powder + 5 grams of Creatine

    Dietary Supplement: Creatine Monohydrate

  • Placebo comparator
    Non Creatine Group

    25 grams of Whey Protein Isolate + 25 grams of Carbohydrate Powder only

    Dietary Supplement: Control

Interventions

  • Dietary supplementCreatine Monohydrate

    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.

  • Dietary supplementControl

    A 25-gram dose of whey protein isolate + 25-gram dose of carbohydrate powder (ProCarb)

06

What researchers measure

Primary outcomes

  1. Time to completion

    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.

    Time frame: 24 Days

  2. Time Trial

    A maximal effort, 3.5 km time trial on an air-braked cycle ergometer (Assault Bike, As-sault Fitness Products, Carlsbad, CA, USA).

    Time frame: 24 Days

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Study locations

1 site
  • Fire Department
    La Crosse, Wisconsin 54601, United States
08

References and documents

Individual participant data

Plan to share: Undecided — Deidentified data is available upon request.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 15, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06172543
Lead sponsor
Ward Dobbs
Collaborators
Mayo Clinic, Des Moines University, Lindenwood University
Responsible party
Ward Dobbs (Assistant Professor, University of Wisconsin, La Crosse) — Sponsor-investigator
First posted
Dec 15, 2023
Start date
Mar 1, 2023
Primary completion
Aug 1, 2023
Completion
Aug 1, 2023
Last update
Dec 15, 2023

Study contacts

Andrew Jagim, PhD
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2023. You cannot join it, but the record below documents what was studied.

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