Satisfaction With eMotion in a Diverse Group of Women
Completed · Not applicable
Conditions studied: Cardiac Events, Emotions
In brief
The eMotion intervention, developed by the PI, provides training on multiple emotion regulation skills based on leading theories and evidence-based emotion regulation interventions. After initial pilot testing of eMotion, the investigators revised the intervention to make it more relevant to women from diverse backgrounds, as these women are disproportionately impacted by social determinants of health that complicate their recovery. It is important to revise the intervention to be acceptable to women from diverse backgrounds and to address their unique needs. The investigators want to explore if women from diverse backgrounds find the revised intervention relevant, meaningful, and easy to understand and apply to their lives. Their feedback will help investigators further revise the intervention to make it acceptable for this population.
Key facts
- Study ID
- NCT06404866
- Run by
- Indiana University
- People needed
- 5
- Starts
- 2024-06-05
- Expected to finish
- 2024-10-01
- Last updated by the study team
- 2025-08-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- First-time major cardiac event as documented in the medical record
- Lives independently
- Has at least mild symptoms of depression (determined by Patient Health Questionnaire-8 [PHQ-8] scores of 5 or greater) and/or at least mild symptoms of anxiety (determined by the General Anxiety Disorder [GAD-7] scores of 5 or greater).
You may not qualify if…
- Does not understand both spoken and written English
- In palliative care or hospice
- Legally blind
Where it is running
- Eskenazi Hospital — Indianapolis, Indiana, United States
Full record on ClinicalTrials.gov
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