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| ID | Type | Description | Link |
|---|---|---|---|
| A532007 | Other Identifier | UW- Madison | |
| SMPH/FAMILY MED/RES GRANTS | Other Identifier | UW- Madison | |
| Protocol Version 11/16/23 | Other Identifier | UW- Madison |
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The goal of this clinical trial is to see if a mobile phone app can deliver depression treatment to African Americans who are depressed. The main question it aims to answer is if this treatment is effective in reducing symptoms of depression.
Participants will attend six 90-minute weekly classes via an app on their phone, and will be asked to complete surveys every week. Participants can expect to be in the study for four months.
The Oh Happy Day Class-Digital Connections (OHDC-DC) is designed for African American adults experiencing clinical depression (CD). OHDC originally comprised of 13 treatment modules focused on culturally relevant strategies to increase knowledge of depression and healthy coping behaviors aimed at reducing symptoms of clinical depression and improving health outcomes.
The Oh Happy Day Class-Digital Connections (OHDC-DC) comprise of 5 core elements of the OHDC-DC:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Oh Happy Day Class-Digital Connections (OHDC-DC) | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| OHDC-DC | Behavioral | 90-minute-weekly cognitive behavioral psycho-education classes using a mobile phone app over a 6-week period |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Personal Health Questionnaire Depression Scale score | Using the 8 item Personal Health Questionnaire Depression Scale (PHQ-8), participants will rate how much they have been bothered by symptoms on a scale of 0-3 with a possible range of 0 to 24. Higher scores indicate greater degree of depression. | Baseline to one month post-intervention (approximately 12 weeks) |
| Change in Generalized Anxiety Disorder 7-item (GAD-7) score | Using the GAD-7 score, participants will rate how much they have been bothered by symptoms on a scale of 0-3 with a possible range of 0 to 24. Higher scores indicate greater degree of anxiety. | Baseline to one month post-intervention (approximately 12 weeks) |
| Change in Quick Inventory of Depressive Symptomatology (QIDS) | Using the 16-item QIDS, participants will rate how much they have been bothered by symptoms on a scale of 0-3 with a possible range of 0 to 27. Higher scores indicate greater degree of depression. | Baseline to one month post-intervention (approximately 12 weeks) |
| Satisfaction with intervention | Participants will rate their satisfaction with the intervention by answering a 9-item questionnaire with a scale of 1-7 (1= none of the time, 7= all of the time). Higher scores indicate greater satisfaction with the intervention. | 12 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Shari Barlow | Contact | 608-265-4348 | shari.barlow@fammed.wisc.edu |
| Name | Affiliation | Role |
|---|---|---|
| Earlise Ward, PhD | University of Wisconsin, Madison | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Wisconsin | Madison | Wisconsin | 53705 | United States |
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| ID | Term |
|---|---|
| D003863 | Depression |
| D003866 | Depressive Disorder |
| ID | Term |
|---|---|
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
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