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Enduring Happiness and Continued Self-Enhancement (ENHANCE) for COVID-19

A Randomized Controlled Trial of an Online Well-Being Intervention (The ENHANCE Program) for Improving Individuals Health and Well-Being During the COVID-19 Pandemic

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04602832
Acronym
EN-COVID-19
Enrollment
350
Registered
2020-10-26
Start date
2020-10-14
Completion date
2020-12-31
Last updated
2020-11-04

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

Conditions

Well-Being

Keywords

Health and Well-Being, Positive Psychology Intervention, Online Bibliotherapy

Brief summary

This study is a randomized controlled trial of an online, evidenced-based intervention (the ENHANCE program) that was modified to address the health and well-being challenges of COVID-19. Eligible participants will be randomized into the ENHANCE or Wait-List Control group over a 12-week period. ENHANCE participants will be introduced, and asked to practice, 10 evidenced-based principles and skills of happiness and well-being. Participants will complete an online survey about their health and well-being at baseline, midway (or 6 weeks), post-assessment (or at the end of the 12-week study), and 3-months following the end of the study.

Detailed description

The study is designed as a 12-week, two-armed, randomized controlled trail to assess the efficacy of a COVID-19-modified version of the Enduring Happiness and Continued Self-Enhancement (ENHANCE) program. The ENHANCE program represents a 12-week multi-construct, evidenced-based intervention for improving overall happiness and subjective well-being. The ENHANCE program was modified specifically to address the known health and well-being challenges of the COVID-19 pandemic. Eligible participants will be randomized into either the ENHANCE program or Wait-List Control (WLC) group. ENHANCE participants will be introduced to 10 evidenced-based principles that have been shown to improve health and well-being outcomes. Participants will be further guided to systematically practice these principles in their daily lives using a small-changes approach. WLC participants will be asked to continue life a usual, and provided some additional health and well-being resources that can be accessed online to support current, ongoing distress, if needed. Participants will be asked to complete an online survey about their emotional, social, and physical well-being at baseline (or at the start of the study), midway (or 6-weeks into the study), and at post-assessment (or at the end of the study period). At the end of the study period, all control participants will also be offered the full ENHANCE program. Investigators expect that participants receiving the ENHANCE program will show improvements across all negative (e.g., depression, anxiety) and positive (e.g., life satisfaction, quality of life) variables from baseline to post-study. Investigators further expect there to be immediate positive health and economic outcomes linked to active participation in the ENHANCE program (versus the WLC group). Investigators believe the impacts of this research will include (a) mitigating the risk of a severe onset of mental health problems related to anxiety, depression, post-traumatic stress, and suicide, (b) increasing positive mental health and well-being, and (c) increasing physical health in participants across time.

Interventions

OTHEREnduring Happiness and Continued Self-Enhancement (ENHANCE) for COVID-19

ENHANCE is a 12-session program designed to help improve subjective well-being, especially through the challenges of a pandemic. The ENHANCE program introduces and teaches people about the evidence-based principles and skills that have been shown across decades of research to improve overall health and well-being.

Sponsors

University of Virginia
CollaboratorOTHER
University of Utah
CollaboratorOTHER
University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Individuals who are fluent in English and are 19 years or older.

Exclusion criteria

* N/A

Design outcomes

Primary

MeasureTime frameDescription
Beck Depression Inventory - II (BDI-II)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline mood
Satisfaction With Life Scale (SWLS)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline satisfaction with life
Generalized Anxiety Disorder - 7 (GAD-7)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline anxiety
Patient Health Questionnaire (PHQ-9)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline mood
Perceived Stress Scale (PSS)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline stress
Positive and Negative Affect Scale (PANAS)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline affect
Health Anxiety Inventory Short-Form (HAI-SF)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline anxiety

Secondary

MeasureTime frameDescription
PTSD Checklist for the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (PCL-5)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline trauma-related distress
World Health Organization Quality of Life (WHOQOL - BREF)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline quality of life
European Quality of Life Group - 5 Dimensions - 5 Levels (EQ-5D-5L)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline quality of life
Meaning In Life Questionnaire (MLQ)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline meaning in life
Sleep Disorder Questionnaire (SDQ)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline sleep quality
Measure of Attachment Qualities (MAQ)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline attachment
University of California, Los Angeles Loneliness Scale (UCLA Loneliness Scale)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline loneliness
Insomnia Severity Index (ISI)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline sleep quality
Paffenbarger Physical Activity Questionnaire (PPAQ)Baseline, Mid-assessment (6 weeks), Post-assessment (3 months), Follow-up-assessment (6 months)Change from baseline physical activity

Countries

Canada

Outcome results

None listed

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