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Completed

NCT Number: NCT02417051

The Efficacy of a Brief Resilience Training Program for Hurricane Sandy Disaster Responders

The goal of this project is to adapt and test the efficacy of the National Institute of Environmental Health and Safety (NIEHS) Disaster Worker Resilience Training (DWRT) Program for Superstorm Sandy responders. The DWRT is a brief, 4-5 hour training program designed to improve resilience for stress reactions in active emergency responders. A total of 120 participants will be recruited. 60 will receive the DWRT, and 60 will be assigned to a waitlist control condition. A three-month assessment period will be utilized to enable us to evaluate the effects of the intervention. Participants assigned to the waitlist condition will be offered the option to participant in the course following completion of the 3 month wait period. It is hypothesized that, participants attending the DWRT program, as compared to those in the waitlist condition, will show increased resilience at three months post-intervention as indicated by lower perceived stress, greater posttraumatic growth, more positive health behaviors (e.g., sleep, nutrition, exercise), and fewer new PTSD and depression symptoms. It is predicted that participants attending the DWRT program, as compared to those in the waitlist condition, will demonstrate greater awareness of the mental health effects of disasters, including the symptoms of PTSD and depression. It is predicted that, participants attending the DWRT program, as compared to those in the waitlist condition, will endorse more positive attitudes towards mental health care, including willingness to seek treatment if needed.

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Key information

Conditions

Psychological Stress Behavior Behavioral Symptoms Personal Satisfaction Psychological Well-Being Stress, Psychological

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

This project is a scientific collaboration between the World Trade Center (WTC) Health Program at Stony Brook University (SBU), the Epidemiology Program at North Shore-LIJ Health System (NSLIJ), and Rutgers University. The goal is to adapt and test the efficacy of the National Institute of Environmental Health and Safety (NIEHS) Disaster Worker Resilience Training (DWRT) Program for Sandy responders by leveraging data from the ongoing projects and the expertise of collaborators at these sites. The DWRT program was originally designed for and piloted with responders to the 2010 Deep Water Horizon oil spill. Knowledge from the ongoing Sandy projects will be used to tailor this intervention to address Sandy-specific risk factors and unique features of the responder communities in the New York Metropolitan area. Responders identified from ongoing projects at SBU (N=1500, 50% anticipated eligible) and other current local disaster responders will be targeted for enrollment. The objectives are to: (1) to adapt the DWRT program for this population; (2) recruit and randomly assign responders (N = 120) to the DWRT program or a waitlist control condition; (3) assess the efficacy of this intervention to enhance resilience over a three month period; and (4) host forums with community stakeholders to share information on this program and its outcomes. The expected outcomes are: (1) efficacy data on the DWRT program, and (2) qualitative data on the acceptability of this intervention to Sandy responders. The products are: (1) a final report; (2) articles for publication; (3) abstracts for national conferences; and (4) a training manual, participant workbook, and presenter materials.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participated as a volunteer or professional in Hurricane Sandy relief efforts.
  • Report that they are still an active disaster responder (i.e., they may be called upon to participate in future disaster relief efforts) as either a volunteer or professional.

Exclusion criteria

  • An inability to comprehend the intervention in English.

Treatment and study plan

Disaster Worker Resiliency Training

Behavioral

The Disaster Worker Resilience Training (DWRT) Program is a 4 hour program which consists of a participant training manual, an instructor-training manual, and a digital presentation. It uses adult training techniques that emphasize active participation in individual and group experiential learning activities. The curriculum is organized into a preface and four chapters, each with action oriented learning objectives. Overall program objectives include a demonstrate an ability to: 1) Recognize signs and symptoms of disaster work-related stress, 2) Obtain support through employer and community resources, and 3) Build resilience by using stress reduction and coping strategies.

Other names: Disaster Worker Resilience Training (DWRT) Program

Primary outcomes

  1. Perceived Stress

    Time frame: 3 months post-intervention

    Perceived Stress Scale (PSS; Cohen, Karmarck, and Mermelstein, 1983).

Secondary outcomes

  1. Post-Traumatic Stress Disorder Symptoms

    Time frame: 3 months post-intervention

    PTSD Checklist for DSM-5 (PCL-5; Weathers, Litz, Keane, Palmieri, Marx, & Schnurr, 2013).

  2. Depression Symptoms

    Time frame: 3 months post-intervention

    Patient Health Questionnaire-9 (PHQ-9; Spitzer, Kroenke, & Williams, 1999).

  3. Mental Illness Stigma

    Time frame: 3 months post-intervention

    Attitudes Towards Mental Illness Questionnaire (ATMIQ).

  4. Attitudes Towards Seeking Professional Help

    Time frame: 3 months post-intervention

    Attitudes Towards Seeking Professional Help Survey (ATSPH; Bacon, Fischer & Farina, 1995).

  5. Post-traumatic Growth

    Time frame: 3 months post-intervention

    Post-Traumatic Growth Inventory-Short Form (PTGI-SF; Cann et al., 2010).

  6. Health Promoting Behaviors

    Time frame: 3 months post-intervention

    Health Promoting Lifestyles Profile-II (HPLP-II; Walker, Sechrist, & Pender, 1995).

Sponsors and collaborators

Lead sponsor

Stony Brook University

Other

Collaborators

  • Department of Health and Human Services
  • Northwell Health
  • Rutgers University

Registry information

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Apr 15, 2015
Registry last updated
Dec 16, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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