Status:

COMPLETED

E-Mental Health Adolescent Depression Program (LEAP)

Lead Sponsor:

Patricia Steele

Collaborating Sponsors:

Alberta Centre for Child, Family & Community Research

Alberta Health Services, Calgary

Conditions:

Depression

Eligibility:

All Genders

13-24 years

Phase:

NA

Brief Summary

The purpose of this project is to explore the potential value and practicality of an innovative depression intervention for young people. More specifically, the objectives of this project are: 1. to ...

Detailed Description

Depression in adolescents and young adults is a prevalent illness in Canada and presents a high burden for those affected and their families. In Canada, depressive disorders are on the rise and their ...

Eligibility Criteria

Inclusion

  • 13-24 years of age
  • meet DSM-IV-TR criteria for major depressive disorder (mild-moderate severity) based on the Children's Depression Rating Scale-Revised or the Hamilton Depression Rating Scale
  • ability to comply with study intervention, provision of informed assent and/or parental consent

Exclusion

  • In order to avoid confounding through a change in the use of mood altering substances or therapies and through underlying medical conditions, patients will be excluded for any of the following reasons:
  • change in use of pharma-therapeutic or herbal treatment for depression in the last three month OR during the first 2 months of trial participation (mild to moderately depressed patients who have not had a change in their treatment in the last three months will be eligible to participate if it is foreseeable that their current treatment will continue unchanged for the first 2 months of trial participation)
  • patients currently undergoing a specific psycho-therapeutic treatment that has been shown to be effective for depression (such as Cognitive Behavioral Therapy (CBT) or Interpersonal Therapy (IPT)) or planning to start such therapy in the next two months
  • change in the use of medications that have mood altering effects in the last 3 months OR during the first 2 months of trial participation
  • history of bipolar disorder, psychotic disorder or psychotic episodes, personality disorder, multiple suicide attempts; history of ADD/ADHD permitted if stabilized (no longer meets DSM-IV-TR criteria for active ADD/ADHD) for at least 2 months; stabilized treated ADD/ADHD permitted if on regular long acting medication and agree to continue
  • uncontrolled medical conditions in the last 3 months (assessed by qualified physician)
  • high suicide risk
  • DSM-IV-TR diagnosis of substance dependence (except nicotine, caffeine) within past 12-months
  • history of tx resistance to ≥ 2 antidepressant medications when treated for an adequate period with a therapeutic dose
  • recent deaths in the family

Key Trial Info

Start Date :

January 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2012

Estimated Enrollment :

63 Patients enrolled

Trial Details

Trial ID

NCT00985686

Start Date

January 1 2010

End Date

September 1 2012

Last Update

July 29 2015

Active Locations (1)

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1

Canadian Institute of Natural and Integrative Medicine (CINIM)

Calgary, Alberta, Canada, T2M 3T1