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Clinical Trials/NCT05636072
NCT05636072
Recruiting
Not Applicable

The WISER Study: Web Based Methods for Enhancing Resilience

Duke University1 site in 1 country8,000 target enrollmentNovember 1, 2022
ConditionsBurnout

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Burnout
Sponsor
Duke University
Enrollment
8000
Locations
1
Primary Endpoint
Change in Emotional Exhaustion as measured by the 5-item Emotional Exhaustion Scale
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

This is a research study to find out if web-based resilience tools can increase well-being.

Enrolled participants will try out one or more brief positive psychology tools. The tools ask participants to reflect on positive experiences or to do an activity (e.g., write a letter of gratitude). The study is entirely online and participants will be prompted to participate via email or text messages.

The study team is interested in the effects of the tools on stress, depression, and burnout in adults. A set of brief surveys are administered before and after using the tool, and again at follow-up periods (e.g., 1, 3, 6 and 12 months). Surveys are collected electronically using the secure, HIPAA-compliant survey software.

There is no direct benefit to participants for participating in this research study aside from the potential to experience improvements in well-being. Risks are minimal and include the potential to feel emotional or psychological distress when asked questions related to burnout.

Registry
clinicaltrials.gov
Start Date
November 1, 2022
End Date
December 31, 2027
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adults 18 and over are considered eligible for the study. A sub-sample will include employees (including but not limited to frontline caregivers, support staff and management) of the Duke University Health System, as well as external health systems. All participants will be invited to participate in one or more of the online tools. The investigators will allow the participation of any clinical areas/healthcare worker groups whose leaders express interest in building resilience. The investigators are targeting healthcare workers for recruitment in the study, but adults 18+ are eligible to participate in any of these tools. Identification as a healthcare worker or not is part of data collection in every tool.

Exclusion Criteria

  • Adults who are not proficient in English, do not have basic computer skills, or who have prohibitive vision or hearing disabilities will be excluded from this study as they will be incapable of full participation in the intervention and/or the survey process.

Outcomes

Primary Outcomes

Change in Emotional Exhaustion as measured by the 5-item Emotional Exhaustion Scale

Time Frame: Baseline, Day 8, and 1, 6, and 12 month follow-ups

Survey scores are measured on a 1-5 Likert-like agreement scale.

Secondary Outcomes

  • Change in Emotional Recovery as measured by the 4-item Emotional Recovery Scale(Baseline, Day 8, and 1, 6, and 12 month follow-ups)
  • Change in Work-life Integration as measured by the 7-item Work-life Integration Scale(Baseline, Day 8, and 1, 6, and 12 month follow-ups)

Study Sites (1)

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