NCT00099827

Brief Summary

The main objective of this research project is to describe the impact of depression on adolescent and family functioning compared to that of healthy adolescents and to understand the impact of Feedback and Patient Activation (FPA) on teen and family decision-making regarding seeking care for depressive disorders.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
368

participants targeted

Target at P75+ for phase_1 depression

Timeline
Completed

Started Oct 2003

Typical duration for phase_1 depression

Geographic Reach
1 country

8 active sites

Status
completed

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

October 1, 2003

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

December 21, 2004

Completed
Same day until next milestone

First Posted

Study publicly available on registry

December 21, 2004

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2006

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2006

Completed
Last Updated

October 18, 2011

Status Verified

October 1, 2011

Enrollment Period

2.9 years

First QC Date

December 21, 2004

Last Update Submit

October 14, 2011

Conditions

Depression

Keywords

Depression

Outcome Measures

Primary Outcomes (1)

  • Receipt of Care

    September 30, 2007

Secondary Outcomes (2)

  • Journal Article

    September, 2007

  • Journal Articles

    September, 2007

Interventions

EducationBEHAVIORAL

Individuals will receive information about depression

Eligibility Criteria

Age13 Years - 17 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Between the ages of 13-17
  • Attending School
  • Living with parent or guardian
  • Reads and writes English
  • Receiving care at a participating PCP office

You may not qualify if:

  • Pregnancy
  • Parents don't speak English or Spanish

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (8)

Family Care Specialists at White Memorial Medical Center

Los Angeles, California, 90033, United States

Location

Northeast Valley Health Corporation-San Fernando Valley High School

San Fernando, California, 91340, United States

Location

Children's National Medical Center Adolescent Health Clinic

Washington D.C., District of Columbia, 20010, United States

Location

Children's Pediatricians and Associates

Washington D.C., District of Columbia, 20037, United States

Location

Capital Medical Group

Chevy Chase, Maryland, 20815, United States

Location

Kaiser Mid-Atlantic

Kensington, Maryland, 20895, United States

Location

Kaiser Mid-Atlantic

Rockville, Maryland, 20852, United States

Location

Kaiser Mid-Atlantic-Camp Springs

Temple Hills, Maryland, 20748, United States

Location

MeSH Terms

Conditions

Depression

Interventions

Educational Status

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Study Officials

  • Audrey Burnam, PhD

    RAND

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
NONE
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

December 21, 2004

First Posted

December 21, 2004

Study Start

October 1, 2003

Primary Completion

September 1, 2006

Study Completion

September 1, 2006

Last Updated

October 18, 2011

Record last verified: 2011-10

Locations

US(8)