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The First Twenty for Volunteer Firefighters

The First Twenty for Volunteer Firefighters

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03181321
Enrollment
419
Registered
2017-06-08
Start date
2014-11-01
Completion date
2018-04-30
Last updated
2018-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Cardiovascular Diseases, Occupational Injuries

Keywords

nutrition, fitness, cardiovascular disease, firefighters, obesity, injury

Brief summary

The purpose of this study is to assess the efficacy of an internet-based firefighter health and wellness program for volunteer fire departments.

Detailed description

A national sample of volunteer fire departments will be recruited for a 6 month, CRCT with a cross-over treatment design to determine the efficacy of The First Twenty (TF20), a wellness program focused on nutrition and fitness for firefighters. Modifications to the existing TF20 will be made to enhance the health coaching features and include tools for program evaluation. Study outcomes (changes in weight, BMI, body fat percentage, waist circumference, dietary intakes, blood pressure, and fitness activities) will be assessed pre- and post-intervention. This will be the first internet-based, occupationally tailored health and wellness program implemented for the volunteer fire service. TF20 will be an essential cost effective tool to address the epidemic of unhealthy body composition, nutrition and fitness among firefighters.

Interventions

The TF20 incorporates individual goal setting and health coaching, leveraging cultural aspects of the fire service and group cohesion to motivate behavior change. The TF20 focuses on the unique needs of FF with culturally relevant nutrition and fitness strategies. TF20 was primarily designed as a cost-effective, stand-alone program for departments which have no health promotion initiative. Program components include practical approaches to nutrition, fitness and mental health.

Sponsors

National Development and Research Institutes, Inc.
CollaboratorOTHER
The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

The investigators will conduct a 6 month, two-arm, CRCT: TF20 vs. Control (which will receive delayed treatment after 6 months). Eligible fire departments volunteering for the trial will be randomized to one of the two study treatment arms. Treatment outcomes will be assessed at baseline and 6 months by our staff.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* first responder within a participating fire department * willing to complete all assessments * internet accessibility through a computer, tablet or smartphone and ability to use devices appropriately

Exclusion criteria

\- not a first responder within a participating fire department

Design outcomes

Primary

MeasureTime frameDescription
Change in Body Mass Index (BMI)baseline, 6 monthsBMI from measured height and weight
Change in Body Fat Percentagebaseline, 6 monthsbody fat % from Tanita scale measurement
Change in Waist Circumferencebaseline, 6 monthswaist circumference from measured waist using a tape

Secondary

MeasureTime frameDescription
Change in Food and nutrient intake as assessed by the Food Frequency Questionnaire (FFQ)baseline, 6 monthsThe Food and Frequency Questionnaire (FFQ) is a self-administered, semi-quantitative, food frequency questionnaire developed by the principal investigator. The FFQ presents a food list, which contains items contributing most to selected nutrient intakes among firefighters and foods encouraged by the intervention. FFQ data will be used to calculate usual nutrient intakes using the Food Intake Analysis System (FIASMe).
Change in self reported physical activity and inactivitybaseline, 6 monthsSRPA

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026