Supportive Expressive Therapy for Depressed and Anxious Adolescents
1 other identifier
interventional
20
1 country
1
Brief Summary
The purpose of the study is to investigate the effectiveness of providing Supportive Expressive Therapy to adolescents who are depressed and/or anxious.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable depression
Started Jan 2004
Longer than P75 for not_applicable depression
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2004
CompletedFirst Submitted
Initial submission to the registry
September 26, 2006
CompletedFirst Posted
Study publicly available on registry
September 28, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2007
CompletedOctober 22, 2015
September 1, 2015
3.8 years
September 26, 2006
October 21, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
BDI
pre and post
MASC
pre and post
Measures collected at pre, post, and follow-up
pre and post
Secondary Outcomes (6)
YSR
pre and post
CBCL
pre and post
FAM
pre and post
CRI
pre and post
SSRS
pre and post
- +1 more secondary outcomes
Study Arms (1)
1
EXPERIMENTALset
Interventions
Eligibility Criteria
You may qualify if:
- year old, male \& female adolescents, primary diagnosis of depression or anxiety disorder.
- Clients with co-morbid diagnoses, suicidal ideation or taking medication would not necessarily be excluded if deemed able to partake in the proposed therapy.
- Medication dose needs to be stable for 4-6 weeks prior to starting therapy.
You may not qualify if:
- Clients who are actively psychotic, developmentally delayed, or have a diagnosis of bipolar disorder.
- Clients who are not fluent in English.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Centre for Addiction and Mental Health
Toronto, Ontario, M5T1R8, Canada
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- psychologist
Study Record Dates
First Submitted
September 26, 2006
First Posted
September 28, 2006
Study Start
January 1, 2004
Primary Completion
October 1, 2007
Study Completion
October 1, 2007
Last Updated
October 22, 2015
Record last verified: 2015-09