Audio-based intervention for reducing depression symptoms
Audio-based Mental Health Intervention Study
This study tests whether an audio program can help adults with moderate or higher depression feel better compared to a self-monitoring approach.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 126 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Penn State University Academic / other |
| Locations | 1 site (University Park, Pennsylvania) |
| Trial ID | NCT05555745 on ClinicalTrials.gov |
What this trial studies
This study evaluates an audio-based digital intervention aimed at alleviating depressive symptoms in adults. Participants with moderate or higher depression will be randomly assigned to either a behavioral activation intervention or a self-monitoring control intervention. The effectiveness of these interventions will be assessed at multiple time points, including baseline, mid-intervention, post-intervention, and follow-up. The study seeks to understand how these audio-based approaches can impact mental health outcomes.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 or older who exhibit moderate to severe depressive symptoms.
Not a fit: Patients with mild depression or those unable to engage with English-language audio content may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could provide an accessible and effective tool for individuals struggling with depression.
How similar studies have performed: Other studies have shown promise with audio-based interventions for mental health, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult age 18 or older * Score in the moderate or higher range on the BDI-FastScreen * Moderate or higher depression confirmed by DIAMOND interview * Proficient English reading, writing, and speaking ability * Able to provide consent * Provide informed consent Exclusion Criteria: * Below 18 years of age * Score below the moderate range on the BDI-FastScreen * DIAMOND interview does not confirm moderate or higher depression * Unable to read, write, and speak in English * Unable to provide consent * Do not provide informed consent
Where this trial is running
University Park, Pennsylvania
- The Pennsylvania State University — University Park, Pennsylvania, United States (Recruiting)
Study contacts
- Study coordinator: Gavin Rackoff, M.S.
- Email: gnr18@psu.edu
- Phone: 814-863-0115
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.