Psychological Distress Clinical Trial
Official title:
Testing the Effectiveness of an Online Behavioral Intervention in Reducing Loneliness
NCT number | NCT04112225 |
Other study ID # | 16 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | August 1, 2019 |
Est. completion date | March 25, 2020 |
Verified date | August 2020 |
Source | Happify Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will use a longitudinal randomized experimental design. Participants will be randomly assigned to either a positive affect skills intervention or a psychoeducation control group and assessed with questionnaires at baseline and immediately post 8-week intervention.
Status | Completed |
Enrollment | 890 |
Est. completion date | March 25, 2020 |
Est. primary completion date | March 25, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - No prior experience on the Happify platform (new user registration) - Located in the United States - Self reported loneliness/desire to be more connected to others Exclusion Criteria: - Participants who are under the age of 18, reside outside of the United States, have previously registered for Happify, or did not self report loneliness/desire to be more connected with others |
Country | Name | City | State |
---|---|---|---|
United States | Happify (an online platform -- study is entirely online) | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Happify Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Loneliness (Revised UCLA Loneliness Scale; Russell, Peplau, & Cutrona, 1980) | A 20-item scale designed to measure one's subjective feelings of loneliness as well as feelings of social isolation. | From start of 8-week intervention (baseline) to immediately post-intervention | |
Secondary | Depression Patient Health Questionnaire (PHQ-9; Kroenke, Spitzer, & Williams, 2001) | A 9-item measure of depressive symptoms | From start of 8-week intervention (baseline) to immediately post-intervention | |
Secondary | Generalized Anxiety Disorder Screener (GAD-7; Spitzer, Kroenke, Williams, & Löwe, 2006) | A 7-item measure of anxiety symptoms | From start of 8-week intervention (baseline) to immediately post-intervention | |
Secondary | Perceived Stress Scale (PSS: Cohen, Kamarck, & Mermelstein, 1983) | 10-item measure of perceived stress | From start of 8-week intervention (baseline) to immediately post-intervention | |
Secondary | Resilience(composite of Perceived Stress Scale [Cohen et al., 1983], Happify Scale [Carpenter et al., 2016] and Life Orientation Scale, Revised [Scheier & Carver, 1985]) | Composite score made of perceived stress, positive emotionality, and optimism. Perceived stress was measured using the Perceived Stress Scale (PSS; Cohen, Kamarck, & Mermelstein, 1983), a 10-item questionnaire that asks users to rate on a scale of 0 (never) to 4 (very often) how frequently they experience various symptoms of feeling stress. Positive emotionality was measured using the emotion subscale of the Happify Scale (HS-E; Carpenter, Crutchley, Zilca, Schwartz, Smith, Cobb, & Parks, 2016), which is a 4-item scale asking participants to rate the extent to which, over the past week, they have experienced positive and negative emotions that are activated or de-activated. Optimism was measured using the Life Orientation Scale, Revised (LOT-R; Scheier & Carver, 1985), a 6-item scale on which participants rate the extent to which they identify with optimistic or pessimistic beliefs. | From start of 8-week intervention (baseline) to immediately post-intervention |
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