NCT00962273

Brief Summary

The purpose of this study is to determine the effects of an interactive, computerized learning resource designed to increase resilience in hospital-based health care workers preparing for an influenza pandemic. The effects of the learning resource will be compared to a non-interactive learning resource condition and a control condition. It is hypothesized that (a) online pandemic-related education reduces absenteeism and interpersonal problems for healthcare workers (HCWs), and improves their pandemic self-efficacy in the short and long-term, and (b) an interactive format for online education is necessary for its benefits.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
118

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2009

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 18, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

August 19, 2009

Completed
1 month until next milestone

Study Start

First participant enrolled

October 1, 2009

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2010

Completed
Last Updated

August 19, 2010

Status Verified

August 1, 2010

Enrollment Period

9 months

First QC Date

August 18, 2009

Last Update Submit

August 17, 2010

Conditions

Keywords

health personnelcommunicable diseasesstress, psychologicalresilience, psychologicaldisaster planningeducationonline

Outcome Measures

Primary Outcomes (1)

  • Absenteeism

    32 weeks

Secondary Outcomes (2)

  • Pandemic self-efficacy

    32 weeks

  • Interpersonal problems

    32 weeks

Study Arms (3)

Pandemic Stress Vaccine - Interactive

EXPERIMENTAL
Behavioral: Interactive computerized learning resource

Pandemic Stress Vaccine - Didactic

ACTIVE COMPARATOR
Behavioral: Didactic computerized learning resource

Wait list

NO INTERVENTION

Some participants are assigned to an eight week waiting condition prior to the course commencing.

Interventions

In a series of interactive scenarios, participants can "see" themselves in stressful work situations that could arise during an influenza pandemic and reflect on effective ways to work out personal and interpersonal difficulties.

Pandemic Stress Vaccine - Interactive

In a non-interactive format (i.e., a series of audio presentations with accompanying PowerPoint-type slides) participants are given information on how to handle stressful work situations that could arise during an influenza pandemic.

Pandemic Stress Vaccine - Didactic

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • employee or professional staff of a hospital

You may not qualify if:

  • unable to read and write English

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mount Sinai Hospital

Toronto, Ontario, M5G 1X5, Canada

Location

Related Publications (1)

  • Maunder RG, Lancee WJ, Balderson KE, Bennett JP, Borgundvaag B, Evans S, Fernandes CM, Goldbloom DS, Gupta M, Hunter JJ, McGillis Hall L, Nagle LM, Pain C, Peczeniuk SS, Raymond G, Read N, Rourke SB, Steinberg RJ, Stewart TE, VanDeVelde-Coke S, Veldhorst GG, Wasylenki DA. Long-term psychological and occupational effects of providing hospital healthcare during SARS outbreak. Emerg Infect Dis. 2006 Dec;12(12):1924-32. doi: 10.3201/eid1212.060584.

MeSH Terms

Conditions

Stress, PsychologicalCommunicable Diseases

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorInfectionsDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • William J. Lancee, Ph.D.

    MOUNT SINAI HOSPITAL

    PRINCIPAL INVESTIGATOR
  • Robert G. Maunder, M.D.

    MOUNT SINAI HOSPITAL

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

August 18, 2009

First Posted

August 19, 2009

Study Start

October 1, 2009

Primary Completion

July 1, 2010

Study Completion

July 1, 2010

Last Updated

August 19, 2010

Record last verified: 2010-08

Locations