Agile Development of Innovative, Interactive Hazard Recognition and Mitigation Tools/Learning E-platforms for Workers Involved in Disaster Rescue and Recovery

July 11, 2024 updated by: William B Perkison, The University of Texas Health Science Center, Houston
The goal of this study is to assess Pocket Ark (PA), which is a mobile e-learning and assessment platform for use by flood remediation workers in the field. The purpose of the mobile application is to provide workers with real-time data to assist with making safe decisions during the planning phase in the flooded zone and provide a communications platform to improve logistics between operational bases and workers during and after the deployment to the flooded zone. Pocket Ark incorporates an action planner, scenario-based PPE training content, assessments (both knowledge and health-risk), personal security protection, and resource location features for workers involved in disaster rescue and recovery. Individual construction worker's readiness to be safely deployed to flooded and post-flood environments will be assessed.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

Enrolled participants will be asked to complete: 1) basic demographic and occupational health information; 2) a simulated wage contract with an employer; 3) a pre-behavioral capability test; and 4) a post flood disaster scenario, which is based on an actual flooding event that has occurred. Participants will be asked questions regarding their response to different challenges he/she might encounter in a post flood construction event and then the correct answer will be provided for learning. Information will be largely graphical, and workers can take the module over the course of several days. Educational material will be based on the Federal Emergency Management Agency (FEMA) Emergency Management Institute and the Center for Construction Research and Training disaster preparedness programs.

Finally, participants will complete: 5) a post behavioral capability test and 6) a brief medical questionnaire of the participant's medical history. Based on the results of the educational testing and the completed medical response, a Readiness Index will be calculated for the participant and relayed to both the participant and the worker advocacy organization. This readiness index will be derived from achieving a passing score of 70% of behavioral capability on the educational and scenario modules, successful completion of the health screening questionnaire, and successful completion of a wage contract.

A brief acceptability assessment and exit interview survey will be completed by participants, and it will assess the program's usefulness, evaluate for technical glitches encountered, request suggestions for future implementation, and derive ratings on PA perceived impact.

Additionally, a worker advocacy staff member who normally conducts disaster preparedness training and a member of the worker advocacy program upper management will be asked to go through the training and answer questions regarding program usability from their perspective.

Study Type

Interventional

Enrollment (Estimated)

64

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 Contact

Study Contact Backup

Study Locations

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Reconstruction workers
  • Affiliated members of the worker advocacy organization
  • Professional experience working in the construction industry
  • Have a 3- year or newer version cell phone capable of accessing the internet
  • Has not completed a Resilience Force training in the last 2 years

Exclusion Criteria:

  • inability to complete requested activities
  • lack of cell phone connectivity

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: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Pocket Ark
Pocket Ark (PA) is a mobile e-learning and assessment platform for use by flood remediation workers in the field. The purpose of this mobile application is to provide workers with real-time data to assist with making safe decisions during the planning phase in the flooded zone and provide a communications platform to improve logistics between operational bases and workers during and after the deployment to the flooded zone. Pocket Ark incorporates an action planner, scenario-based PPE training content, assessments (both knowledge and health-risk), personal security protection, and resource location features for workers involved in disaster rescue and recovery. Individual construction worker's readiness to be safely deployed to flooded and post-flood environments will be assessed.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of participants who have increased behavioral capability as assessed by a survey
Time Frame: baseline, after completion of Pocket Ark education (within 2 hours of baseline)
A survey will be used to assess the worker's procedural knowledge on the steps and skills to negotiate a contract and meet criteria for operational readiness for post-flood clean-up.
baseline, after completion of Pocket Ark education (within 2 hours of baseline)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Usability of the Pocket Ark mobile application as assessed by the Technology Acceptance Model (TAM)
Time Frame: after completion of Pocket Ark education (within 2 hours of baseline)
Total score on the Technology Acceptance Model (TAM) ranges from 5 to 25, with a lower the score indicating greater usability.
after completion of Pocket Ark education (within 2 hours of baseline)
Usability of the Pocket Ark mobile application as assessed by the System Usability Scale (SUS)
Time Frame: after completion of Pocket Ark education (within 2 hours of baseline)
Total score on the System Usability Scale (SUS) ranges from 0 to 100, with a higher score indicating greater usability.
after completion of Pocket Ark education (within 2 hours of baseline)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: William B Perkison, MD, The University of Texas Health Science Center, Houston

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 (Estimated)

July 11, 2024

Primary Completion (Estimated)

July 12, 2024

Study Completion (Estimated)

July 12, 2024

Study Registration Dates

First Submitted

May 8, 2023

First Submitted That Met QC Criteria

July 11, 2024

First Posted (Actual)

July 15, 2024

Study Record Updates

Last Update Posted (Actual)

July 15, 2024

Last Update Submitted That Met QC Criteria

July 11, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • HSC-SPH-23-0741
  • R44ES030580 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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