- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07475988
Adapting a Telehealth Intervention for Suicide Prevention Among Patients With Alcohol Use Disorder in Tanzania (IDEAS-AUD)
March 12, 2026 updated by: Duke University
Adapting a Telehealth Intervention for Suicide Prevention Among Patients With Alcohol Use Disorder in Tanzania: IDEAS-AUD
Together, alcohol use and suicide account for approximately 4 million deaths per year, with a considerable burden on low and middle-income countries.
Tanzania is among the world's most underserved nations for mental health treatment, with very little capacity to treat suicidality or alcohol use disorders.
In this study, the researchers will adapt an evidence-based intervention for suicide prevention to address the unique needs of people with alcohol use disorders in Tanzania, and rigorously pilot test the intervention to assess its feasibility and acceptability in a Tanzanian emergency department.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Globally, alcohol use disorders (AUD) cause 3.3 million deaths each year and account for nearly 100 million disability-adjusted life years (DALYs).
Alcohol use is also one of the most prominent risk factors for death by suicide, as people with AUD have a lifetime risk of suicide more than 7 times higher than the general population.
In preliminary studies at Kilimanjaro Christian Medical Centre (KCMC) in Tanzania, 7% of patients with AUD met criteria for comorbid depression, 7% were experiencing suicidal thoughts or behavior, and nearly half reported challenges in social support.
Unfortunately, Tanzania is also among the most underserved nations in the world for mental health treatment, with fewer than 1 psychologist or psychiatrist per 1 million people and very little capacity to intervene for suicide risk or AUD.
Given this shortage in treatment, there is a critical need for innovative, resource-efficient treatments for suicide prevention among people with AUD.
In Tanzania, 91% of the population owns a cellular phone and nearly 50% use mobile internet, yet telehealth interventions have been largely unexplored, representing a major missed opportunity for delivering evidence-based interventions.
By adapting an evidence-based Motivational Interviewing intervention, MI-SafeCope, the team developed IDEAS for Hope, a telehealth intervention for suicide prevention in HIV care in Tanzania.
In the current grant, the researchers propose to revisit this process by adapting MI-SafeCope, with lessons learned from the HIV study, to reduce suicide risk among people with AUD who are presenting for care in the KCMC Emergency Department (ED).
The resulting intervention, IDEAS-AUD, will address suicide risk with a four-pillared approach: reducing alcohol-related harm, building social support, enhancing emotional health, and addressing social determinants of health.
The pillars are integrated with Motivational Interviewing-enhanced safety planning and referral for local psychiatric care as appropriate.
The long-term goal is to create evidence-based, accessible, and cost-effective treatments for mental health and substance use treatment in low-resource settings.
The objectives of this proposal are to: 1) adapt IDEAS-AUD for the AUD population in Kilimanjaro, Tanzania; 2) rigorously evaluate the acceptability and feasibility of IDEAS-AUD; and 3) develop the intervention package, along with a trialability evaluation, for a future implementation evaluation and clinical trial.
In Aim 1 of the current study, the researchers will identify drivers of suicide risk and desired intervention characteristics to prevent suicide in the AUD population at KCMC.
In Aim 2, the study team will adapt an evidence-based suicide prevention intervention to existing AUD care, guided by a community coalition.
In Aim 3, the investigators will pilot test the telehealth intervention to assess its feasibility and acceptability for reducing suicide risk in the KCMC AUD population.
By the end of this proposed project, the researchers will have a framework-guided, culturally- and resource-adapted, piloted protocol for IDEAS-AUD, including screening tools, programmatic, and implementation components.
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Brandon Knettel, PhD
- Phone Number: 9196601218
- Email: brandon.knettel@duke.edu
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- 18 years of age or older
- screen positive for alcohol use disorder (AUDIT >=8)
- have had suicidal thinking (C-SSRS item indicating "actual thoughts of suicide") in last 30 days
- clinically sober
- medically stable
- have the physical and cognitive capacity to provide consent and complete study procedures
- able to communicate in Swahili or English
Exclusion Criteria:
- prisoners
- decline or unable to complete informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: IDEAS-AUD
3 sessions of telehealth-delivered counseling
|
Telehealth-delivered counseling to reduce suicide risk among people with Alcohol Use Disorder (AUD) who are presenting for care in the KCMC Emergency Department (ED).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acceptability of intervention
Time Frame: 3 months
|
Acceptability of Intervention Measure (AIM).
Four items scored from 1-Completely disagree to 5-Completely agree.
Scores are summed for a total score of 4 to 20, with higher scores indicating greater acceptability.
|
3 months
|
|
Enrollment feasibility as measured by the percentage of ED patients with documented screening for study eligibility
Time Frame: up to 1 year
|
up to 1 year
|
|
|
Enrollment feasibility as measured by the number of eligible participants who declined enrollment
Time Frame: up to 1 year
|
up to 1 year
|
|
|
Enrollment feasibility as measured by the time needed to enroll 30 eligible participants
Time Frame: up to 1 year
|
up to 1 year
|
|
|
Retention feasibility as measured by the number of participants retained for follow-up
Time Frame: session 2 (2 weeks), session 3 (4 weeks), and 3 months
|
session 2 (2 weeks), session 3 (4 weeks), and 3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Brandon Knettel, PhD, Duke University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
August 1, 2027
Primary Completion (Estimated)
March 1, 2029
Study Completion (Estimated)
March 1, 2029
Study Registration Dates
First Submitted
March 12, 2026
First Submitted That Met QC Criteria
March 12, 2026
First Posted (Actual)
March 17, 2026
Study Record Updates
Last Update Posted (Actual)
March 17, 2026
Last Update Submitted That Met QC Criteria
March 12, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pro00118645
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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