- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05745246
Firefighters Preventing Cancer Online Training Program
Firefighters Preventing Cancer: Cluster Randomized Trial of an Online Training Program for Cancer Prevention Behaviors in Volunteer Firefighters
The goal of this two-arm, Cluster Randomized Trial is to evaluate an e-health training program for volunteer firefighters to reduce their risk of exposures to carcinogens and to increase their understanding and intentions of behavior towards cancer prevention. One arm will receive an online e-health intervention for six months and the other arm will be considered as a waitlist control group which will be placed on a waitlist and receive the online treatment program some months later.
The project aims to evaluate the firefighters by measurement of current behavior, perceived importance, future behavioral intentions and perceived barriers for implementing decontamination behaviors at baseline, after the intervention and after 3-month follow-up before and after the intervention.
The intervention consists of three components:
- a novel health information strategy, 90SecondFire Cancer health letters
- a brief on-line course
- a problem-solving asynchronous bulletin board to mobilize existing knowledge
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Firefighters face a serious risk of exposure to carcinogens from products of combustion. Modern materials burn hotter and may be even more toxic than older wood construction. Preventing the increased risk of cancer in volunteer firefighters has raised attention as they are more vulnerable to carcinogen exposure.
The goal of this two-arm, Cluster Randomized Trial is to evaluate an e-health training program for volunteer firefighters to reduce their risk of exposures to carcinogens and to increase their understanding and intentions of behavior towards cancer prevention. One arm will receive an online e-health intervention for six months and the other arm will be considered as a waitlist control group which will be placed on a waitlist and receive the online treatment program some months later. Up to 800 volunteer firefighters from approximately 40 volunteer fire departments in Canada will be recruited for both arms.
The project aims to evaluate the firefighters by measurement of current behavior, perceived importance, future behavioral intentions and perceived barriers for implementing decontamination behaviors at baseline, after the intervention and after 3-month follow-up through an online validated survey: Firefighter Exposure to Carcinogens Scale (FECS).
The intervention consists of three components:
- a novel health information strategy, 90SecondFire Cancer health letters
- a brief on-line course
- a problem-solving asynchronous bulletin board to mobilize existing knowledge
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Nova Scotia
-
Halifax, Nova Scotia, Canada
- IWK Health Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Departments will be screened to meet the following criteria
- Be a Volunteer Department
- Be located in Canada
- Consent to participate in the study via the Chief or delegate
Participant in the CRT study must meet all the following criteria to be eligible to proceed with the study:
- Be a volunteer firefighter
- Working for an all-volunteer fire department that has joined the study
- Live in Canada
- Has access to internet
- Be able to read, write and understand English or French
- Consent to participate in the study
Exclusion Criteria:
The exclusion for Departments
- Not a volunteer Department in other words to be a composite department with some volunteers and some career fire fighters or a department that has not joined the study
- Not located in Canada
- Not Consent to be in the study via the Chief or delegate
Any of the following criteria will exclude individuals from proceeding to consent:
- NOT a volunteer firefighter
- Working for a composite department with some volunteers and some career fire fighters or a department that has not joined the study
- Does NOT live in Canada
- Does not have access to internet
- Is NOT able to read, write and understand English or French
- Does NOT consent to participate in the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Group
This arm will receive the online e-health intervention for six months. The intervention consists of three sections:
|
|
|
No Intervention: waitlist control group
This group will be placed on a waitlist and will receive the online treatment program after six months.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Volunteer Firefighters' Intention to engage in reducing exposure and undertaking decontamination behaviour
Time Frame: Baseline, After 6 month intervention and 3-month follow-up
|
In order to measure the changes in firefighter's intention during the study, the data will be collected by an online survey: Firefighter Exposure to Carcinogens Scale.
The dimensions will be rated on a Likert scale.
min :0 Max 4 ; The higher score does not mean a better outcome.
|
Baseline, After 6 month intervention and 3-month follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Volunteer Firefighters' practice and perceived importance towards reducing exposure and undertaking decontamination behavior for cancer prevention
Time Frame: Baseline, After 6 month intervention and 3-month follow-up
|
The data will be collected by an online survey: Firefighter Exposure to Carcinogens Scale .
The dimensions will be rated on a Likert scale.
min :0 Max 4 ; The higher score does not mean a better outcome.
|
Baseline, After 6 month intervention and 3-month follow-up
|
|
Volunteer firefighters' and their departments' perceived barriers in the development of reducing exposure and undertaking decontamination behaviors
Time Frame: Baseline, After 6 month intervention and 3-month follow-up
|
The data will be collected by an online survey: Firefighter Exposure to Carcinogens Scale .
The dimensions will be rated on a a Likert scale.
min :0 Max 4 ; The higher score does not mean a better outcome.
|
Baseline, After 6 month intervention and 3-month follow-up
|
|
Comparing and detecting any association between the regular volunteer firefighters and the management team towards cancer prevention
Time Frame: Baseline, After 6 month intervention and 3-month follow-up
|
The data will be collected by an online survey: Firefighter Exposure to Carcinogens Scale .
The dimensions will be rated on a Likert scale.
min :0 Max 4 ; The higher score does not mean a better outcome.
|
Baseline, After 6 month intervention and 3-month follow-up
|
|
Comparing characteristics of different volunteer Departments (Clusters) such as size and location of Department in terms of their future intention, current practice and perceived importance towards cancer prevention
Time Frame: Baseline, After 6 month intervention and 3-month follow-up
|
The data will be collected by an online survey: Firefighter Exposure to Carcinogens Scale .
The dimensions will be rated on a Likert scale.
min :0 Max 4 ; The higher score does not mean a better outcome.
|
Baseline, After 6 month intervention and 3-month follow-up
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1028192
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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