NCT05636072

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.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
8,000

participants targeted

Target at P75+ for not_applicable

Timeline
19mo left

Started Nov 2022

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress70%
Nov 2022Dec 2027

Study Start

First participant enrolled

November 1, 2022

Completed
22 days until next milestone

First Submitted

Initial submission to the registry

November 23, 2022

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 5, 2022

Completed
5.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

April 8, 2026

Status Verified

April 1, 2026

Enrollment Period

5.2 years

First QC Date

November 23, 2022

Last Update Submit

April 7, 2026

Conditions

Keywords

BurnoutWell-beingBehavioral Health

Outcome Measures

Primary Outcomes (1)

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

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

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

Secondary Outcomes (2)

  • 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 Arms (2)

Treatment Immediately

EXPERIMENTAL

Participants will engage in well-being tools immediately for 1-week.

Behavioral: WISER

Waitlist Control

NO INTERVENTION

Participants will wait 1 week to begin the well-being tools.

Interventions

WISERBEHAVIORAL

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

Treatment Immediately

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Duke University Health System

Durham, North Carolina, 27707, United States

RECRUITING

Related Publications (5)

  • Seligman ME, Steen TA, Park N, Peterson C. Positive psychology progress: empirical validation of interventions. Am Psychol. 2005 Jul-Aug;60(5):410-21. doi: 10.1037/0003-066X.60.5.410.

    PMID: 16045394BACKGROUND
  • Profit J, Adair KC, Cui X, Mitchell B, Brandon D, Tawfik DS, Rigdon J, Gould JB, Lee HC, Timpson WL, McCaffrey MJ, Davis AS, Pammi M, Matthews M, Stark AR, Papile LA, Thomas E, Cotten M, Khan A, Sexton JB. Randomized controlled trial of the "WISER" intervention to reduce healthcare worker burnout. J Perinatol. 2021 Sep;41(9):2225-2234. doi: 10.1038/s41372-021-01100-y. Epub 2021 Aug 9.

    PMID: 34366432BACKGROUND
  • Adair KC, Kennedy LA, Sexton JB. Three Good Tools: Positively reflecting backwards and forwards is associated with robust improvements in well-being across three distinct interventions. J Posit Psychol. 2020;15(5):613-622. doi: 10.1080/17439760.2020.1789707. Epub 2020 Jul 9.

    PMID: 34295357BACKGROUND
  • Sexton JB, Adair KC, Cui X, Tawfik DS, Profit J. Effectiveness of a bite-sized web-based intervention to improve healthcare worker wellbeing: A randomized clinical trial of WISER. Front Public Health. 2022 Dec 8;10:1016407. doi: 10.3389/fpubh.2022.1016407. eCollection 2022.

    PMID: 36568789BACKGROUND
  • Sexton JB, Adair KC. Well-Being Outcomes of Health Care Workers After a 5-Hour Continuing Education Intervention: The WELL-B Randomized Clinical Trial. JAMA Netw Open. 2024 Sep 3;7(9):e2434362. doi: 10.1001/jamanetworkopen.2024.34362.

    PMID: 39298170BACKGROUND

MeSH Terms

Conditions

Burnout, Psychological

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehavior

Study Officials

  • John B Sexton, PhD

    Duke

    PRINCIPAL INVESTIGATOR

Central Study Contacts

John B Sexton, PhD

CONTACT

Kathryn C Adair, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Waitlist control group Randomized Control Design
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 23, 2022

First Posted

December 5, 2022

Study Start

November 1, 2022

Primary Completion (Estimated)

December 31, 2027

Study Completion (Estimated)

December 31, 2027

Last Updated

April 8, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Only the research team will be accessing the data.

Locations