Actively Recruiting

Age: 18Years - 35Years
All Genders
NCT07052318

Developing a Music Listening mHealth Intervention for Stress Reduction in Early Recovery

Led by Washington State University · Updated on 2025-07-23

30

Participants Needed

1

Research Sites

58 weeks

Total Duration

On this page

Sponsors

W

Washington State University

Lead Sponsor

N

National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The overarching goal of this study is to develop and examine the feasibility of a music-listening intervention that can be deployed in "real time" to regulate emotions and reduce momentary stress among young adults within the first 12 months of recovery from alcohol use disorder. We design the study with two phases to address three aims: Phase I includes the first two aims. For Aim 1, we will conduct formative research with a sample of young adults (N = 30) who have are within 12 months of recovery to identify features of music selections that are most effective in reducing momentary stress in real-world, ambulatory settings. For Aim 2, we will focus on developing mobile health technology that uses passive sensing and machine learning to automatically predict moments of heightened stress in real-time and suggest specific musical selections when stress is detected. During Phase II (Aim 3), we will test the feasibility of a novel music-listening intervention among a second unique sample of young adults who are within 12 months of recovery from AUD (N = 30). This protocol refers only to Phase I of the larger study, which focuses on observing music listening preferences and physiological and mental stress among people in early recovery from alcohol use disorder.

CONDITIONS

Official Title

Developing a Music Listening mHealth Intervention for Stress Reduction in Early Recovery

Who Can Participate

Age: 18Years - 35Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subject can and has signed an Institutional Review Board (IRB) approved informed consent form (ICF).
  • Age 618 and 635 years.
  • In early-stage recovery for alcohol use (within 12 months)
  • Own a smartphone with a data plan
  • Not experiencing symptoms of severe depression
  • Not experiencing thoughts of suicide
  • Meets the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) diagnostic criteria for alcohol use disorder (AUD)
  • Not currently taking medication treatment for opioid use disorder (OUD)
  • Able to speak and read English
Not Eligible

You will not qualify if you...

  • Currently experiencing symptoms of severe depression
  • Currently experiencing thoughts of suicide
  • Currently taking medication treatment for opioid use disorder (OUD)
  • Are unable to provide voluntary informed consent.
  • Cannot read or speak English.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Washington State University Research Clinic

Spokane, Washington, United States, 99202

Actively Recruiting

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Research Team

A

Alex Schmidt

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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