Impact of Team-Based Training on Compliance and Physical Fitness in Firefighters

November 30, 2024 updated by: Shen Xin

Research Objectives: This study aims to develop a team-based training model specifically tailored for firefighters, focusing on improving their cardiovascular fitness, physical attributes, and fostering sustainable health behaviors. The ultimate goal is to reduce the risk of injuries associated with the physically demanding tasks they perform during their duties.

Research Hypotheses:

Firefighters participating in the team-based training model will demonstrate significant improvements in key fitness parameters, such as cardiorespiratory fitness, muscular strength, endurance, and body composition compared to those engaged in traditional training.

The team-based approach will enhance adherence to physical training among firefighters, leading to more consistent participation and improved health outcomes.

This clinical study is a randomized controlled trial that involved 42 firefighters who were divided into two groups: one receiving a team-based training intervention for six months and the other continuing with conventional exercises. The team training incorporated aerobic, resistance, and functional exercises, emphasizing teamwork and peer support to motivate participants. Key fitness measures, including cardiorespiratory fitness, strength, endurance, flexibility, and body mass index (BMI), were assessed before and after the intervention.

The study hypothesized that the team-based training model would not only enhance fitness levels but also improve adherence to training routines among firefighters, ultimately contributing to better health and safety during their demanding work.

Study Overview

Study Type

Interventional

Enrollment (Actual)

40

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 Locations

    • Hunan
      • Changsha, Hunan, China, 410000
        • Changsha Fire Brigade

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

No

Description

Inclusion Criteria:

Firefighters aged 18 to 50 years. Currently active duty within the selected brigade. Capable of performing physically demanding tasks without medical restrictions. Written informed consent provided by participants.

Exclusion Criteria:

Firefighters with any cardiovascular, respiratory, or musculoskeletal conditions that could hinder participation or affect fitness outcomes.

Individuals recovering from recent injuries or surgeries. Firefighters enrolled in external training programs that may impact baseline health assessments.

Any participant who refuses to provide informed consent.

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: Team-Based Training Intervention for Firefighter Fitness and Adherence
This arm involves a six-month team-based training intervention designed to improve firefighters' physical fitness and exercise adherence. The program includes aerobic, resistance, and functional exercises tailored to the demands of firefighting tasks. Sessions are conducted in small groups to foster teamwork and peer support, with participants receiving real-time feedback and guidance from certified professionals. The aim is to enhance cardiovascular fitness, strength, endurance, and overall health behaviors, while reducing injury risks. Participants track their progress using the Gymsmart (Pro X) app to monitor activity levels and adjust intensity for optimal results.

Spanning six months, the program incorporated aerobic training, resistance training, and functional exercises essential for rescue operations. Each training session was led by certified professionals who emphasized adherence to safety protocols and provided real-time feedback.

Central to the training process was the significance of teamwork and mutual support, with sessions conducted in small groups focused on shared objectives. This framework fostered a collaborative environment that promoted peer support and motivated participants to actively engage in their fitness regimen. The group setting enabled firefighters to encourage one another and share individual progress, thereby enhancing their sense of responsibility and belonging.

Experimental: Control group
The control group maintained their old habits
The control group will maintain their original daily habits without any intervention behaviors for them

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximal oxygen consumption (VO2max)
Time Frame: Baseline, 3 months, and 6 months following the intervention.
This primary outcome measure assesses changes in cardiorespiratory fitness among firefighters participating in the team-based training program. Fitness is evaluated using the Gerkin treadmill protocol, which estimates maximal oxygen consumption (VO2max).
Baseline, 3 months, and 6 months following the intervention.
Body composition
Time Frame: Baseline, 3 months, and 6 months following the intervention.
measured using the Inbody770 bioelectrical impedance analyzer, with BMI calculated as weight (kg) divided by height squared (m²);
Baseline, 3 months, and 6 months following the intervention.
Muscular strength
Time Frame: Baseline, 3 months, and 6 months following the intervention.
Grip strength is assessed using a hand dynamometer, with the maximum value recorded from three attempts for each hand.
Baseline, 3 months, and 6 months following the intervention.
Muscular endurance
Time Frame: Baseline, 3 months, and 6 months following the intervention.
Muscular endurance is evaluated through maximum push-ups and sit-ups performed within standardized time limits (2 minutes for push-ups and 3 minutes for sit-ups).
Baseline, 3 months, and 6 months following the intervention.
Flexibility
Time Frame: Baseline, 3 months, and 6 months following the intervention.
Flexibility is assessed using a modified sit-and-reach test, measuring the distance reached beyond the toes while seated.
Baseline, 3 months, and 6 months following the intervention.
Exercise adherence
Time Frame: Baseline, 3 months, and 6 months following the intervention.
Adherence is assessed by tracking the completion of daily training sessions, defined as performing more than 50% of the prescribed exercises and sets.
Baseline, 3 months, and 6 months following the intervention.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

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 (Actual)

March 10, 2024

Primary Completion (Actual)

September 10, 2024

Study Completion (Actual)

September 11, 2024

Study Registration Dates

First Submitted

October 29, 2024

First Submitted That Met QC Criteria

November 30, 2024

First Posted (Estimated)

December 5, 2024

Study Record Updates

Last Update Posted (Estimated)

December 5, 2024

Last Update Submitted That Met QC Criteria

November 30, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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