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Clinical Trials/NCT01905267
NCT01905267CompletedNot Applicable

Mindfulness Intervention to Study the Neurobiology of Depression

University of Illinois at Chicago2 sites in 1 country33 target enrollmentStarted: March 2013Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
33
Locations
2
Primary Endpoint
Change in Children's Depression Rating Scale - Revised

Study Overview

Brief Summary

The Pediatric Mood Disorders Program at the University of Illinois at Chicago is conducting a research study examining how mindfulness can help teenagers stay healthy and prevent depression relapse.

Detailed Description

Study involves:

  • Brain scan using fMRI technology
  • Questions about mood and behavior
  • Meeting with a clinician
  • Possibility of 8 weekly treatment sessions using mindfulness
  • Ongoing assessment of depression for next 2 years

Eligible participants will be compensated for their time.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
12 Years to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • between the ages of 12 and 18
  • history of major depressive disorder

Exclusion Criteria

  • afraid of small spaces

Arms & Interventions

Treatment

Experimental

Participants randomized to the experimental condition will receive 8 weeks of individual treatment with Rumination-Focused Cognitive Behavior Therapy

Intervention: Rumination-Focused Cognitive Behavior Therapy (Behavioral)

Control

No Intervention

Participants randomized to the control arm will complete questionnaires and receive mood monitoring for the duration of the study

Outcomes

Primary Outcomes

Change in Children's Depression Rating Scale - Revised

Time Frame: Baseline, 8 week

clinician measure completed with adolescent and parent Total scores reported. Range is between 17-119 Higher scores mean higher depressive symptoms

Secondary Outcomes

  • Change in Reynolds Adolescent Depression Scale(Baseline, 8 week)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rachel Jacobs

Research Assistant Professor, Licensed Clinical Psychologist

University of Illinois at Chicago

Study Sites (2)

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