NCT06597032

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

87
On Track

Trial Health Score

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

Enrollment
11,659

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

September 11, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 19, 2024

Completed
8 days until next milestone

Study Start

First participant enrolled

September 27, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2025

Completed
Last Updated

May 7, 2025

Status Verified

May 1, 2025

Enrollment Period

4 months

First QC Date

September 11, 2024

Last Update Submit

May 2, 2025

Conditions

Keywords

Positive AffectResilience ChallengePositive PsychologyStress

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

EXPERIMENTAL

The 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.

Behavioral: Resilience Challenge

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).

Resilience Challenge

Eligibility Criteria

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

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

Location

Study Officials

  • Judith T Moskowitz

    Northwestern University

    PRINCIPAL INVESTIGATOR

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

Locations