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Sustainability Strategies for Suicide Prevention (Sust-AIns Trial)
N/A
Waitlist Available
Led By Emily E. Haroz, PhD
Research Sponsored by Johns Hopkins Bloomberg School of Public Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Over the age of 18
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Sust-AIns Trial Summary
This trial will test different ways to help mental and behavioral health programs stay effective in tribal communities, using a mix of qualitative and quantitative methods.
Who is the study for?
This trial is for adults over 18 who speak English and are knowledgeable about implementing suicide prevention programs. Participants must be able to attend study meetings and assessments. Those under the influence, with active psychosis or mania, or any condition preventing informed consent cannot join.Check my eligibility
What is being tested?
The study tests sustainment strategy interventions designed to keep evidence-based mental and behavioral health programs running in tribal communities. It uses a combination of qualitative and quantitative research methods to evaluate these strategies.See study design
What are the potential side effects?
Since this trial focuses on sustainability strategies rather than medical treatments, traditional side effects associated with medications are not applicable here.
Sust-AIns Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am over 18 years old.
Sust-AIns Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Program Sustainability Assessment Tool
Sust-AIns Trial Design
1Treatment groups
Experimental Treatment
Group I: InterventionExperimental Treatment1 Intervention
Interrupted time series design
Find a Location
Who is running the clinical trial?
Johns Hopkins Bloomberg School of Public HealthLead Sponsor
410 Previous Clinical Trials
2,116,902 Total Patients Enrolled
Emily E. Haroz, PhDPrincipal InvestigatorJohns Hopkins Bloomberg School of Public Health
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am not under the influence, do not have active psychosis or mania, and can fully consent.I am over 18 years old.
Research Study Groups:
This trial has the following groups:- Group 1: Intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is this experiment presently enrolling participants?
"Based on what is posted on clinicaltrials.gov, this medical trial has stopped recruiting participants as of the last edit from October 4th 2022. While no longer open to enrollment, there are currently 168 other trials actively looking for qualified individuals."
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