Depression Clinical Trial
— EAITDASOfficial title:
Effectiveness and Acceptability of Internet-delivered Treatment for Depression, Anxiety and Stress in University Students: Protocol for an Open Feasibility Trial
| NCT number | NCT02614443 |
| Other study ID # | EAITDAS |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | October 2015 |
| Est. completion date | September 2017 |
| Verified date | September 2018 |
| Source | Silver Cloud Health |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aims of this study are to test the effectiveness and acceptability of internet-delivered
treatment for depression, anxiety and stress in university students. These data will inform
the methods for a future randomized controlled trial.
The trial will establish an initial estimate of the effectiveness of these online
interventions for students in terms of within-group effect sizes associated with changes in
depression, anxiety and stress from pre to post-intervention and follow-up. These data will
be used to estimate the sample size for a future trial to ensure that the study is
sufficiently powered. A conservative estimate using the 90% upper confidence limit will be
used to inform the sample size calculation of the definitive RCT.
Acceptability of the intervention to participants will be assessed using data on usage and
engagement with the intervention (e.g. percentage of participants completing each module,
average number of log ins, average time spent per session and total time spent on the
program). These data are acquired through the online SilverCloud system. Satisfaction with
will be assessed through the use of a post-intervention questionnaire on satisfaction with
accessing and using an online delivery format for treatment.
| Status | Completed |
| Enrollment | 120 |
| Est. completion date | September 2017 |
| Est. primary completion date | September 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Participants must be at least 18 years of age. Participants must have self-reported mild to severe symptoms of depression (5-27+) according to PHQ-9, self-reported mild to severe symptoms of anxiety (5-21+) according to GAD-7, or self-reported mild to severe symptoms of stress (15-34+) according to the stress sub-scale of DASS-21. Exclusion Criteria: - Students who currently are in face-to-face therapy at UCCS or BHS will be excluded. Students who score in the "red zone" in terms of risk of self-harm on the screening questions routinely used at UCCS will not be referred to the study. Students who score greater than 0 on the PHQ-9 self-harm item during the initial screening phase will be automatically directed to be further evaluated and alerted that a counselor will try to reach them. Based on this further evaluation, they may be recommended to seek help from their health/counseling service and may/may not be eligible to participate in the study. They will be telephoned within 1 working day and contacted by email if they cannot be reached by phone. |
| Country | Name | City | State |
|---|---|---|---|
| United States | University of Minnesota | Minneapolis | Minnesota |
| Lead Sponsor | Collaborator |
|---|---|
| Silver Cloud Health |
United States,
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* Note: There are 24 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Change in The Satisfaction with Treatment (SAT) Questionnaire | Satisfaction measure containing two qualitative questions asking participants to describe what they most liked and least liked about the online treatment. | Postintervention at 8 weeks and 3 month follow-up | |
| Primary | Change in Stress sub-scale of Depression Anxiety and Stress Scale-21 (DASS-21) | Composed of 7-item sub-scale measuring symptoms of stress. | Baseline, postintervention at 8 weeks and 3 month follow-up | |
| Primary | Change in Patient Health Questionnaire-9 (PHQ-9) | A self-report measure of depression that has been widely used in screening, primary care, and research. | Baseline, postintervention at 8 weeks and 3 month follow-up | |
| Primary | Change in Generalized Anxiety Disorder-7 (GAD-7) | Comprises 7 items measuring symptoms and severity of GAD based on the DSM-IV diagnostic criteria for GAD. | Baseline, postintervention at 8 weeks and 3 month follow-up |
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