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Clinical Trials/NL-OMON48325
NL-OMON48325
Recruiting
Not Applicable

StayFine: a personalized monitoring and intervention app to prevent relapse of anxiety and mood disorders in youth and young adults - StayFine: relapse prevention of anxiety and mood disorders in youth

niversiteit Utrecht0 sites254 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
niversiteit Utrecht
Enrollment
254
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria at entry of the study:
  • \- Age of 13\-21 years
  • \- Daily access to a mobile phone with iOs or Android software
  • \- Adolescents do NOT currently meet criteria of a current anxiety disorder
  • (separation \-, social \- or generalized anxiety disorder, specific phobia, panic
  • disorder, agoraphobia) or depressive disorder (major depressive \-, persistent
  • depressive \-, disruptive mood dysregulation disorder or other specified
  • depressive disorder) based on a semi\-structured diagnostic interview (K\-SADS),
  • but DO meet the criteria for at least one previous episode of one or the

Exclusion Criteria

  • A potential subject who currently meets criteria of any of the following mental
  • health problems will be excluded from participation in this study:
  • \- alcohol or drug misuse
  • \- previous hypomania and/or mania
  • \- bipolar disorder
  • \- previous and/or current psychotic episode , Other exclusion criteria include:
  • \- only in remission of PTSD or OCD, or of another anxiety or mood disorder than
  • mentioned above at the inclusion criteria, namely premenstrual dysphoric
  • disorder, depressive disorder due to another medical condition,
  • substance/medication\-induced depressive disorder, unspecified depressive

Outcomes

Primary Outcomes

Not specified

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