Anxiety Clinical Trial
Official title:
Randomized Control Trial of Online Mental Health Promotion Program for University Students
Verified date | May 2023 |
Source | University of California, Los Angeles |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study was a randomized controlled trial of an original online mental health promotion program. This study aimed to: 1) establish program effectiveness by examining symptom change between conditions and 2) examine predictors of symptom change. The program was previously tested in open trial feasibility study by the same Principal Investigator and has since been rebuilt as informed by feasibility findings and participant qualitative feedback. Participants were randomly assigned to either a waitlist condition or eight weeks of the intervention condition. Baseline, posttest, and follow-up electronic surveys collected self-reported symptoms of stress, anxiety, and depression. Motivational variables were also assessed at baseline and then tested as moderators of intervention effects.
Status | Completed |
Enrollment | 1631 |
Est. completion date | March 18, 2018 |
Est. primary completion date | March 18, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - enrolled as a student at UCLA (Fall 2017 - Winter 2018) Exclusion Criteria: - concurrent enrollment in a similar online anxiety and depression treatment study on campus - invalid data reporting (e.g., straight-lined responses to surveys) -- post hoc exclusion |
Country | Name | City | State |
---|---|---|---|
United States | University of California, Los Angeles | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Los Angeles |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Subjective Happiness Scale | This 4-item self-report measure assesses subjective happiness. Individual items are rated 1 to 7, with total scores ranging 4 - 28. Higher scores at posttest relative to baseline indicate improvement. | [Time Frame: Baseline to Posttest (~8 weeks)] | |
Other | Patient Health Questionnaire-9 | This 9-item self-report measure assesses symptoms of major depressive disorder. Individual items are rated 0 (Not at all) to 3 (Nearly every day), with total scores ranging 0 - 27. Lower scores at posttest relative to baseline indicate improvement. | [Time Frame: Baseline to Posttest (~8 weeks)] | |
Primary | Depression Anxiety and Stress Scale (DASS-21) | This 21-item self-report measure assesses symptoms of depression, anxiety, and stress. Individual items are rated 0 (Did not apply to me at all) to 3 (Applied to me very much or most of the time), with total scores ranging 0 - 63. Lower scores at posttest relative to baseline indicate improvement. | [Time Frame: Baseline to Posttest (~8 weeks)] | |
Secondary | Program Adherence | This outcome was assessed based on number of modules with 1+ skills practice log. Skills practice logs were recorded as behavioral data, stored within the online platform's database of user account activity. | [Time Frame: Baseline to Posttest (~8 weeks)] | |
Secondary | Program Satisfaction | This 5-item measure was adapted from the Client Satisfaction Questionnaire. Individual items are rated 1 (Poor) to 4 (Excellent), with total scores ranging 5 - 20. Higher scores indicate more satisfaction. | Posttest (~8 weeks) |
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