Influence of a Corrective Exercise Training Program on Measures of Functional Movement Among Active-Duty Firefighters

November 12, 2016 updated by: Kyle T Ebersole, University of Wisconsin, Milwaukee

The occupation of firefighting is considered to be one of the most dangerous occupations in the United States (U.S.). As such, a high prevalence of musculoskeletal injuries (MSKIs) have been observed among the firefighter population. This high rate of MSKI has created an extremely large financial impact on fire departments across the United States. Therefore, interest in developing methods of identifying those at risk for developing a future MSKI and interventions designed to prevent these MSKIs from happening has grown among both the firefighter population, as well as among researchers and practitioners.

Previous research has demonstrated relationships between MSKI and altered movement patterns. In addition, researchers have started to demonstrate the ability of functional movement assessments to predict future MSKI in various populations, including firefighters. Two of these functional movement assessments include the Functional Movement Screen (FMS) and the Movement Efficiency (ME) Test, which is a component of the Fusionetics Human Performance System. These assessments both quantify the overall functional movement quality of an individual by creating a composite movement score (i.e., Total FMS & Average ME Test scores, respectively).

In addition, various theoretical models of corrective exercise programming have been proposed. These programs are designed to restore optimal neuromuscular control and correct any identified neuromuscular imbalances observed during the movement assessment through the use of simple and easy-to-follow exercises. The Fusionetics Human Performance System utilizes one such model, with the goal of improving the functional movement quality of an individual by correcting the aforementioned neuromuscular deficiencies observed during the ME Test. Based on this framework, these corrective exercise programs theoretically lower the risk of MSKI of the individual as well.

However, there is currently a lack of research in the literature examining the influence of corrective exercise programming on functional movement quality among the active-duty firefighter population. As such, it remains unknown if a corrective exercise intervention is capable of significantly improving functional movement quality among active-duty firefighters. In addition, recent research suggests that various health and fitness measures are associated with functional movement quality. These measures include total body power output, lower extremity muscular strength, and core muscular endurance. As such, an examination of the influence of a corrective exercise intervention on measures of health and fitness among active-duty firefighters is warranted.

Study Overview

Status

Unknown

Study Type

Interventional

Enrollment (Actual)

51

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

    • Wisconsin
      • Milwaukee, Wisconsin, United States, 53205
        • Station 5

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

General Eligibility Criteria:

Participants will be considered eligible for this study if they:

  1. are fluent in speaking and writing English;
  2. are at least 18 years of age;
  3. they are an active-duty firefighter;
  4. are cleared by their fire department for full active-duty work; and
  5. have been an active-duty firefighter for at least 12 months (i.e., one year).

Inclusion Criteria:

Participants will be included into this study if they:

  1. do not suffer from chest pain or dizziness;
  2. have not been diagnosed with a heart condition;
  3. are not currently pregnant;
  4. have not had any serious ankle, knee, hip, back, or shoulder trauma that required medical attention in the past 3 months;
  5. have not had surgery on their ankle, knee, hip, back, or shoulder within the past year (12 months); or
  6. do not have any current bone, joint, or muscle abnormalities that require medical attention;
  7. have not been instructed by a physician or their Health and Safety Officer (HSO) to not participate in this study.

Exclusion Criteria:

1. Participants will be excluded from being placed into Phase 2 (i.e., the intervention portion) of this study if they are already engaged in a structured corrective exercise program. Furthermore, in order to ensure similar baseline functional movement quality between the CEP and CON groups, participants will be excluded from being placed into the intervention portion of this study if their Overall MET score is < 25 or > 75.

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: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Corrective Exercise Program
Participants in the Corrective Exercise Program (CEP) group (n = 28) will be given a four-week corrective exercise programming intervention.
Participants will be given a four-week corrective exercise protocol, with four corrective exercise sessions prescribed each week. Participants in the CEP Group will be required to complete a minimum of three of these four training sessions per week throughout the four-week corrective exercise program intervention. All corrective exercise programming will be created through the Fusionetics Human Performance System. This system, along with weekly compliance questionnaires, will also assess the compliance-level among the participants.
No Intervention: Control
The participants in the Control (CON) group (n = 28) will have their four-week corrective exercise programming intervention deferred for 4 weeks, and as such, will serve as the comparative group for the CEP group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Total Functional Movement Screen (FMS) Score
Time Frame: Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
The Functional Movement Screen (FMS) is a seven task movement screen test that will be scored on a 4-point scale (0-3, worst-best), for a total of 21 possible points.
Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
Change in Overall Movement Efficiency (ME) Test Score
Time Frame: Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
The Movement Efficiency (ME) Test, which is part of the Fusionetics Human Performance System, uses a 0-100 scale to score the functional movement quality of an individual.
Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
Change in Dynamic Balance Ability
Time Frame: Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
The dynamic balance ability of each participant will be assessed by utilizing the Y-Balance Test (YBT).
Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Range of Motion
Time Frame: Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
Passive range of Motion (PROM) for the foot, ankle, knee, hip, shoulder, and trunk will be bilaterally measured with a standard plastic goniometer (a kind of ruler).
Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
Change in Total Body Power Output
Time Frame: Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
Total body power output will be examined by performing a countermovement jump (CMJ), which is a field-test commonly utilized by practitioners to examine total body power output.
Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
Change in Lower Extremity Isometric Muscular Strength
Time Frame: Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
The isometric lower extremity muscular strength of each participant will be examined utilizing the Jackson Strength Evaluation System.
Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
Change in Core Muscular Endurance
Time Frame: Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)
The overall core muscular endurance of each participant will be examined through the use of a prone plank. Participants will perform a prone plank until volitional fatigue.
Pre-Intervention (Week 0), Mid-Intervention (Week 3), Post-Intervention (Week 5)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Kyle T. Ebersole, Ph.D., University of Wisconsin, Milwaukee

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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

July 1, 2015

Primary Completion (Anticipated)

May 1, 2017

Study Completion (Anticipated)

May 1, 2018

Study Registration Dates

First Submitted

August 27, 2015

First Submitted That Met QC Criteria

February 2, 2016

First Posted (Estimate)

February 3, 2016

Study Record Updates

Last Update Posted (Estimate)

November 15, 2016

Last Update Submitted That Met QC Criteria

November 12, 2016

Last Verified

November 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • 15.389

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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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