Skip to content

Development and testing of a suicide risk prevention program for people who use alcohol.

Development and feasibility testing of a suicide risk prevention intervention for alcohol users. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/111521
Enrollment
45
Registered
2026-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: F101- Alcohol abuse

Interventions

Intervention1: Suicide Risk Prevention Intervention for Alcohol Users: A structured behavioral intervention including psychoeducation, coping skills training, emotional regulation, and psychosocial su

Sponsors

JSS Academy of Higher Education Research Mysuru
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged 18 years and above diagnosed with Alcohol Use Disorder (AUD) according to clinical criteria. Participants must be identified at an elevated risk of suicide using the Columbia-Suicide Severity Rating Scale (C-SSRS), with eligibility restricted to individuals scoring 4 or higher (representing a severity threshold greater than 50%). Participants must demonstrate explicit willingness to actively participate in the behavioral intervention module and commit to the scheduled follow-up assessments.

Exclusion criteria

Exclusion criteria: 1.Individuals experiencing acute psychotic symptoms (e.g., hallucinations, delusions) or manic episodes, as these may interfere with participation and informed consent. 2.Individuals not meeting the AUD criteria or not at suicide risk as per C-SSRS. 3.Individuals with severe cognitive impairment, traumatic brain injury, severe neurological conditions, delirium tremens, or alcohol-related severe medical conditions (e.g., Wernicke s encephalopathy, advanced liver failure) that limit their ability to participate in behavioral interventions. 4.Primary dependence on substances other than alcohol (e.g., opioids, stimulants) as the main clinical concern. 5.Participants requiring immediate psychiatric hospitalization due to imminent or active suicide risk (e.g., active plan and means) will be excluded and referred for emergency care. 6.Severe or terminal illnesses (e.g., advanced liver disease, cancer) that would limit the participant s ability to attend sessions or complete follow-up. 7.Participants unwilling or unable to adhere to the structured suicide prevention protocol or complete required follow-ups.

Design outcomes

Primary

MeasureTime frame
Change in suicide risk scores measured using the Columbia-Suicide Severity Rating Scale (C-SSRS).Timepoint: Baseline, 5 weeks (immediate post-intervention), and 9 weeks (4 weeks post-intervention follow-up).

Secondary

MeasureTime frame
Changes in scores for alcohol dependence (SAD-Q), readiness to change (SOCRATES), depression (BDI-II), anxiety (BAI), coping strategies (Brief COPE), suicide stigma (SOSS), & perceived social support (MSPSS).Timepoint: Baseline, 5 weeks (immediate post-intervention), & 9 weeks (4 weeks post-intervention follow-up)

Countries

India

Contacts

Public ContactVedavathi

JSS Medical College and Hospital

pradeepkumarpc@jssuni.edu.in9964223388

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026