The Resilience Challenge: Fostering Emotional Resilience During a Time of National Stress
FERN
The Resilience Challenge: FERN (Fostering Emotional Resilience During a Time of National Stress)
1 other identifier
interventional
11,659
1 country
1
Brief Summary
The goal of this clinical trial is to examine the effects of an online positive psychological intervention on positive emotion, anxiety, depression, feelings of social isolation, sleep disturbance and a sense of meaning and purpose in the general public. The main question it aims to answer is: Will the practice of positive emotion skills via a self-guided online platform reduce feelings of anxiety, depression, social isolation, and sleep disturbance, as well as increase well-being, positive emotion, a sense of meaning and purpose, life satisfaction, and general self-efficacy? Participants will take part in an online positive psychological skill learning intervention for 6-8 weeks. Prior to beginning, immediately after, and 4 weeks after, participants will fill out measures of their wellbeing.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2024
Shorter than P25 for not_applicable
1 active site
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
September 11, 2024
CompletedFirst Posted
Study publicly available on registry
September 19, 2024
CompletedStudy Start
First participant enrolled
September 27, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2025
CompletedMay 7, 2025
May 1, 2025
4 months
September 11, 2024
May 2, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
PROMIS Positive Affect CAT
At baseline, after completion of 6-8 week intervention, and 4 weeks later
Secondary Outcomes (7)
PROMIS Depression CAT
At baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS Anxiety CAT
At baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS Meaning and Purpose CAT
At baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS Social Isolation CAT
At baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS Sleep Disturbance CAT
At baseline, after completion of 6-8 week intervention, and 4 weeks later
- +2 more secondary outcomes
Study Arms (1)
Resilience Challenge
EXPERIMENTALThe Resilience Challenge Study is an online program containing a series of positive emotion skills for individuals experiencing stress and distress during their everyday life. The online program specifically targets positive emotion and offers an array of skills in a self-guided online delivery platform. Participants will, over the course of 6-8 weeks, access weekly skill lessons, daily homework, and daily emotion reporting. The skill lessons will include: positive events, savoring, gratitude, everyday mindfulness, mindfulness meditation, positive reappraisal, self-compassion, personal strengths, and attainable goals.
Interventions
We previously have tested this online program in people facing health- and work-related stressors (e.g., dementia caregivers, healthcare workers), and in 2020 we enrolled adults in a test of the online program to support coping with the stress of the COVID pandemic. This intervention has been tailored for a widespread, public audience (e.g., we have added a few other safety measures including limits on public forum posting and have clarified wording on some of the intervention content to make it clearer and easier to understand).
Eligibility Criteria
You may qualify if:
- Over 18 years old, Access to device connected to the internet
You may not qualify if:
- Under 18 years old
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Northwestern University Feinberg School of Medicine
Chicago, Illinois, 06011, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Judith T Moskowitz
Northwestern University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Medical Social Sciences
Study Record Dates
First Submitted
September 11, 2024
First Posted
September 19, 2024
Study Start
September 27, 2024
Primary Completion
January 31, 2025
Study Completion
April 1, 2025
Last Updated
May 7, 2025
Record last verified: 2025-05