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Depression Outcomes Study of Exercise (DOSE)

Primary Purpose

Unipolar Depression

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Public Health Dose of Exercise (PHD)
Low Dose Exercise (LD)
Sponsored by
National Institute of Mental Health (NIMH)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Unipolar Depression focused on measuring adolescents, exercise, depression, dose response, pilot study

Eligibility Criteria

12 Years - 21 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Primary Diagnosis of DSM-IV Major Depression Disorder (MDD)
  • Child Depression Rating Scale Revised > or = 40 at final screen
  • 12 to 21 years of age
  • On a stable dose of antidepressants or ADHD medication only
  • Physically capable of exercise according to AHA and ACSM standards
  • Able to pass illicit drug screen
  • Perform < 20 minutes per day of moderate to vigorous physical activity
  • Parental consent and participant assent
  • Denver metropolitan area including Jefferson county

Exclusion Criteria:

  • Chronic disease that would limit exercise
  • Other psychiatric illness
  • Suicidal or homicidal
  • Concurrent psychotherapy
  • Two previous failed SSRI trials or a failed trial of CBT
  • Current pregnancy or breastfeeding

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Public Health Dose of Exercise (PHD)

    Low Dose Exercise (LD)

    Arm Description

    17.5 kcal per kilogram per week

    7.0 kcal per kilogram per week

    Outcomes

    Primary Outcome Measures

    Child Depression Rating Scale-Revised (CDRS-R)

    Secondary Outcome Measures

    Beck Depression Inventory (BDI)
    The Multidimensional Anxiety Scale for Children (MASC)
    Adolescent Stress Questionnaire (ASQ)

    Full Information

    First Posted
    August 20, 2009
    Last Updated
    March 13, 2013
    Sponsor
    National Institute of Mental Health (NIMH)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00964054
    Brief Title
    Depression Outcomes Study of Exercise
    Acronym
    DOSE
    Official Title
    Adapting Exercise Treatment for Depression to Adolescents: A Pilot Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2012
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2012 (undefined)
    Primary Completion Date
    January 2013 (Actual)
    Study Completion Date
    February 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    National Institute of Mental Health (NIMH)

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This pilot study may yield important research findings on how to adapt exercise treatment for depression among adolescents. Potential public health benefits from this study include a reduction of adolescent depression and problems associated with untreated depression in young adults including suicide, substance abuse, cigarette smoking, teen pregnancy, impaired psychosocial functioning and school failure. In addition, because this study prescribes physical activity as a treatment for depression, additional public health benefits may include a reduction in chronic diseases such as obesity, diabetes and heart disease, all of which are associated with sedentary behavior.
    Detailed Description
    Adolescent depression is a major public health problem in the United States and throughout the world. Major depressive disorder (MDD) in adolescence is common with point prevalence rates of 3% to 9%. In the U.S., it is estimated that by the time adolescents reach the age of 17, 14% will have experienced at least one episode of major depressive disorder. Effective treatments of adolescent depression are clearly needed despite the fact that in the past 10-15 years, there has been a dramatic increase in studies of the efficacy of medications, primarily the selective serotonin reuptake inhibitors (SSRIs) and of cognitive behavioral therapy (CBT). Medications and CBT rarely result in complete and lasting remission of symptoms, and residual symptoms are associated with a high rate of relapse. In most studies, a positive response is defined as a 30-50% improvement in symptoms and/or a global rating that the subject is much or very much improved. In adults, exercise has been used as a mono-therapy and as an augmentation therapy with antidepressant medication. Our recently completed randomized trial of exercise treatment in adults found response and remission rates of 46% and 42%, in those randomized to a public health dose of exercise. In adolescents, data on the use of exercise to treat MDD is relatively sparse. A 2006 Cochrane review of exercise to prevent and treat depression in adolescents found a small effect size in support of exercise, but the conclusion is based on evidence from a small number of randomized clinical trials of low methodological quality. In this exploratory R34, the specific aims of this application are to: 1) Develop a detailed Manual of Procedures (MOP) to conduct an acute-phase randomized trial of exercise to treat adolescent depression; 2) Develop estimates of recruitment yield from tests of various recruitment strategies; and, 3) Pilot test trial methodologies in (n=40) adolescents diagnosed with depression to ascertain estimates of treatment effect sizes, adherence and drop-out rates. To achieve these aims, the project is organized into 3 phases. Phase I will be the development of the first draft MOP that will adapt procedures developed from a previous trial examining two doses of exercise in treatment of adult MDD. Phase II will test specific recruitment methodologies to determine recruitment yields for each strategy and will pilot test screening procedures developed in Phase I. Phase III will be a pilot test of the intervention and will include development of baseline and outcome measures of exercise and depression; development and implementation of the experimental exercise treatment; and determination of the effects of exercise on depressive symptoms. Following the pilot study, we will finalize all procedures for the MOP and obtain estimates of effect sizes, adherence and drop out rates. These data will allow us to specify all study procedures necessary to meet standards of high methodological quality for a future, larger-scale, controlled study of exercise in depressed youth and will provide us with needed experience.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Unipolar Depression
    Keywords
    adolescents, exercise, depression, dose response, pilot study

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    InvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    9 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Public Health Dose of Exercise (PHD)
    Arm Type
    Experimental
    Arm Description
    17.5 kcal per kilogram per week
    Arm Title
    Low Dose Exercise (LD)
    Arm Type
    Active Comparator
    Arm Description
    7.0 kcal per kilogram per week
    Intervention Type
    Other
    Intervention Name(s)
    Public Health Dose of Exercise (PHD)
    Other Intervention Name(s)
    Exercise, Physical Activity
    Intervention Description
    17.5 kcal per kilogram per week
    Intervention Type
    Other
    Intervention Name(s)
    Low Dose Exercise (LD)
    Other Intervention Name(s)
    Exercise, Physical Activity
    Intervention Description
    7.0 kcal per kilogram per week
    Primary Outcome Measure Information:
    Title
    Child Depression Rating Scale-Revised (CDRS-R)
    Time Frame
    repeated measures, 12-weeks
    Secondary Outcome Measure Information:
    Title
    Beck Depression Inventory (BDI)
    Time Frame
    repeated measures, 12 weeks
    Title
    The Multidimensional Anxiety Scale for Children (MASC)
    Time Frame
    baseline and 12 weeks
    Title
    Adolescent Stress Questionnaire (ASQ)
    Time Frame
    baseline and 12 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    12 Years
    Maximum Age & Unit of Time
    21 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Primary Diagnosis of DSM-IV Major Depression Disorder (MDD) Child Depression Rating Scale Revised > or = 40 at final screen 12 to 21 years of age On a stable dose of antidepressants or ADHD medication only Physically capable of exercise according to AHA and ACSM standards Able to pass illicit drug screen Perform < 20 minutes per day of moderate to vigorous physical activity Parental consent and participant assent Denver metropolitan area including Jefferson county Exclusion Criteria: Chronic disease that would limit exercise Other psychiatric illness Suicidal or homicidal Concurrent psychotherapy Two previous failed SSRI trials or a failed trial of CBT Current pregnancy or breastfeeding
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Andrea L Dunn, PhD
    Organizational Affiliation
    Klein Buendel, Inc.
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Depression Outcomes Study of Exercise

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