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The Resilience Challenge: Fostering Emotional Resilience During a Time of National Stress

The Resilience Challenge: FERN (Fostering Emotional Resilience During a Time of National Stress)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06597032
Acronym
FERN
Enrollment
11659
Registered
2024-09-19
Start date
2024-09-27
Completion date
2025-04-01
Last updated
2025-05-07

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

Conditions

Positive Affect, Stress

Keywords

Positive Affect, Resilience Challenge, Positive Psychology, Stress

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.

Interventions

BEHAVIORALResilience Challenge

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).

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Over 18 years old, Access to device connected to the internet

Exclusion criteria

* Under 18 years old

Design outcomes

Primary

MeasureTime frame
PROMIS Positive Affect CATAt baseline, after completion of 6-8 week intervention, and 4 weeks later

Secondary

MeasureTime frame
PROMIS Depression CATAt baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS Anxiety CATAt baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS Meaning and Purpose CATAt baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS General Life Satisfaction CATAt baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS Sleep Disturbance CATAt baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS General Self-Efficacy CATAt baseline, after completion of 6-8 week intervention, and 4 weeks later
PROMIS Social Isolation CATAt baseline, after completion of 6-8 week intervention, and 4 weeks later

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026