Audio-based intervention for reducing depression symptoms

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• 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

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.