Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06608498
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-19
Brief Title:
DMHI for At-Risk College Students
Sponsor:
None
Organization:
None
Study Overview
Official Title:
User-Centered Design of a Single-Module Digital Mental Health Intervention for College Students At Risk for Psychosis
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical trial is to learn if a single-session digital intervention SPARK Coping is acceptable usable and demonstrates a preliminary signal of efficacy in reducing symptom-related distress and increasing positive treatment-seeking attitudes among college students reporting subthreshold symptoms associated with risk for psychosis Research questions inclue
Does SPARK Coping reduce symptom-related distress and increase positive treatment seeking attitudes primary outcomes relative to a waitlist control condition
Does SPARK Coping increase adaptive coping and reduce internalized stigma primary targets relative to a waitlist control condition
Researchers will compare provision of SPARK Coping to a waitlist control condition and collect data from participants on each of the variables described above Participants will
Complete questionnaires and surveys remotely at the start of the study and two weeks later
Be offered access to the SPARK Coping intervention either after completion of their baseline assessment intervention arm or after two weeks waitlist control arm
Does SPARK Coping reduce symptom-related distress and increase positive treatment seeking attitudes primary outcomes relative to a waitlist control condition
Does SPARK Coping increase adaptive coping and reduce internalized stigma primary targets relative to a waitlist control condition
Researchers will compare provision of SPARK Coping to a waitlist control condition and collect data from participants on each of the variables described above Participants will
Complete questionnaires and surveys remotely at the start of the study and two weeks later
Be offered access to the SPARK Coping intervention either after completion of their baseline assessment intervention arm or after two weeks waitlist control arm
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None