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The WISER Study: Web Based Methods for Enhancing Resilience

The WISER Study: Web Based Methods for Enhancing Resilience

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05636072
Enrollment
8000
Registered
2022-12-05
Start date
2022-11-01
Completion date
2027-12-31
Last updated
2026-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burnout

Keywords

Burnout, Well-being, Behavioral Health

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.

Interventions

BEHAVIORALWISER

Participants will engage in one or more positive psychology well-being tool(s).

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Waitlist control group Randomized Control Design

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Emotional Exhaustion as measured by the 5-item Emotional Exhaustion ScaleBaseline, Day 8, and 1, 6, and 12 month follow-upsSurvey scores are measured on a 1-5 Likert-like agreement scale.

Secondary

MeasureTime frameDescription
Change in Emotional Recovery as measured by the 4-item Emotional Recovery ScaleBaseline, Day 8, and 1, 6, and 12 month follow-upsSurvey scores are measured on a 1-5 Likert-like agreement scale.
Change in Work-life Integration as measured by the 7-item Work-life Integration ScaleBaseline, Day 8, and 1, 6, and 12 month follow-upsSurvey scores are measured with a 1-4 frequency of behaviors scale.

Countries

United States

Contacts

CONTACTJohn B Sexton, PhD
bryan.sexton@duke.edu+1 919 681 4949
CONTACTKathryn C Adair, PhD
Kathryn.C.Adair@duke.edu+1 919 681 4949
PRINCIPAL_INVESTIGATORJohn B Sexton, PhD

Duke

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 9, 2026