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Standardized Adaptive Music Medicine for Suicidality

Standardized Adaptive Music Medicine for Suicidality

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07610785
Acronym
STAMM-S
Enrollment
28
Registered
2026-05-28
Start date
2026-06-01
Completion date
2027-05-01
Last updated
2026-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicidal Thoughts and Behaviors

Keywords

Suicidality, Music-based intervention, Music

Brief summary

The primary goal of this clinical trial is to test if music-based intervention (STAMM-S) works for individuals with suicidal thoughts or behaviors. The main questions it aims to answer are: * Can implementing specific music to listen to for 20 minutes a day for 25 days improve suicidality? * Can implementing education around the psychology of the medicine of music improve mental health outcomes? Participants will: * Listen to music given to them by the study team for 20 minutes a day for 25 days * Receive musical psychoeducation on how to improve mood using music

Interventions

BEHAVIORALSTAMM-S

Participants will undergo the STAMM-S treatment, which involves music generated using machine learning to move to a more positive affect. They will also receive education on how to best use the music assigned to improve their mood.

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
14 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

1. Age 14-35 years 2. Suicidal ideation (C-SSRS categories 1-3 within the past month) 3. normal sensitivity to music reward on the Barcelona Music Reward Questionnaire. Score \>65

Exclusion criteria

1. imminent or acute suicide risk (C-SSRS categories 4-5). 2. Co-morbid substance use disorder. 3. Co-morbid psychotic disorder. 4. current participation in another trial

Design outcomes

Primary

MeasureTime frameDescription
Change in Suicidality via Beck Scale for Suicidal Ideation (BSS/BSSI) ScoreBaseline, week 1, week 2, week 3, and post-trial interview (up to 25 days).A 19-item scale with each item scoring from 0-2 rating an individual's suicidal thoughts, intent, and ideation. The total score ranges from 0 to 38. A higher score indicates more intense suicidal ideation and a low score indicates less intense suicidal ideation.
Change in Generalized Anxiety Disorder Status via Generalized Anxiety Disorder-7 (GAD-7) ScoreBaseline, week 1, week 2, week 3, and post-trial interview (up to 25 days).A 7-item measure scaled 0-3 per item that measures symptoms of Generalized Anxiety Disorder. 0 would be no sign of anxiety and 3 would indicate high level of anxiety over the last two weeks.
Change in Depression Status via Patient Health Questionnaire-9 (PHQ-9) ScoreBaseline, week 1, week 2, week 3, and post-trial interview (up to 25 days).A 9-item questionnaire that measures symptoms of depression on a 0-3 scale over the last two weeks. 0 would indicate "not at all", 1 would indicate "several days", 2 would indicate "most of the days", and a 3 would indicate "nearly every day".

Secondary

MeasureTime frameDescription
Change in Music Listening Purpose via Healthy-Unhealthy Music Scale (HUMS) - Healthy ScoreBaseline, end of study (up to 25 days).Participants respond to a 5-question survey. The scale ranges from 5 to 25. For the healthy scale, a higher rating means a healthier use of music.
Change in Music Listening Purpose via Healthy-Unhealthy Music Scale (HUMS) - Unhealthy ScoreBaseline, end of study (up to 25 days).Participants respond to an 8-question survey. The scale ranges 8 to 40. A higher rating for the unhealthy scale indicates a more maladaptive use of music.
Acceptability Scale ScoreAt the end of the intervention (25 days after enrollment).A 7-question questionnaire on a scale of 0-7 covering the 7 core components on intervention acceptability, where a 0 would indicate total unacceptability and 7 would equal total acceptability. Single participant rating of 4 or greater will be interpreted as satisfactory acceptability.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORDaniel L. Bowling, PhD

Stanford University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 29, 2026