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immi for Mental Health
N/A
Waitlist Available
Led By Jose A Bauermeister, PhD
Research Sponsored by University of Pennsylvania
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4-week follow-up
Awards & highlights
Study Summary
This study is evaluating whether a web application can help improve the mental health of sexual and gender minority youth.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4-week follow-up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4-week follow-up
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Coping Self-efficacy
Secondary outcome measures
Anxiety Symptoms
Cognitive and Behavioral Coping Skills
Depression Symptoms
+3 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: immiExperimental Treatment1 Intervention
The intervention is a novel and scalable web application designed to provide sexual and gender minority youth with tools for affirming their identity and coping with minority stress.
Group II: Online Resource websiteActive Control1 Intervention
The comparator is a website that includes a list of freely available web-based resources for sexual and gender minority youth.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
immi
2021
N/A
~270
Find a Location
Who is running the clinical trial?
University of PennsylvaniaLead Sponsor
2,009 Previous Clinical Trials
42,894,383 Total Patients Enrolled
1 Trials studying Mental Health
1,520 Patients Enrolled for Mental Health
HopeLab FoundationOTHER
6 Previous Clinical Trials
1,832 Total Patients Enrolled
Jose A Bauermeister, PhDPrincipal InvestigatorUniversity of Pennsylvania
3 Previous Clinical Trials
1,215 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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