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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01905267
Other study ID # 2012-0689
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2013
Est. completion date June 2017

Study information

Verified date October 2017
Source University of Illinois at Chicago
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date June 2017
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender All
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria:

- between the ages of 12 and 18

- history of major depressive disorder

Exclusion Criteria:

- braces

- afraid of small spaces

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Rumination-Focused Cognitive Behavior Therapy
This intervention targets rumination and other maladaptive forms of emotion regulation such as suppression and avoidance and provides skills training in effective coping strategies. Mindfulness is a key component of this intervention as a strategy for disengaging from one's thoughts. Strategies from Dialectical Behavior Therapy (DBT), such as the use of effective interpersonal skills, are also included as methods for regulating strong emotion. Rumination-Focused Cognitive Behavior Therapy is a structured, manual based program designed to be delivered weekly over eight weeks. Sessions are 60-90 minutes in length.

Locations

Country Name City State
United States University of Illinois at Chicago Pediatric Mood Disorders Program Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Illinois at Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Children's Depression Rating Scale - Revised clinician measure completed with adolescent and parent Total scores reported. Range is between 17-119 Higher scores mean higher depressive symptoms Baseline, 8 week
Secondary Change in Reynolds Adolescent Depression Scale Self report adolescent depression total score. Range is 30-120 with higher scores meaning greater depressive symptoms. Baseline, 8 week
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