Actively Recruiting

Phase Not Applicable
Age: 14Years - 17Years
All Genders
NCT03859297

Mechanisms of Rumination Change in Adolescent Depression

Led by Ohio State University · Updated on 2025-08-11

183

Participants Needed

3

Research Sites

513 weeks

Total Duration

On this page

Sponsors

O

Ohio State University

Lead Sponsor

U

University of Exeter

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will evaluate whether a newer treatment, rumination-focused cognitive behavioral treatment, which includes mindfulness and can be used to reduce ruminative habits, change ways in which key brain regions interact with each other (e.g.., often called connectivity), and whether these changes in habits and brain connectivity can reduce the risk for recurrence of depression in the next two years.

CONDITIONS

Official Title

Mechanisms of Rumination Change in Adolescent Depression

Who Can Participate

Age: 14Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Previous diagnosis of Major Depressive Disorder (full or partial remission for at least two weeks) confirmed by KSADSPL
  • Rumination Responsiveness Scale score above age and sex specific mean (T > 50)
  • Age 14 to 17 years at enrollment
  • Postpubertal as assessed by Petersen Pubertal Developmental Scale
  • Youth assent and parent consent obtained
  • Intellectual Quotient (IQ) above 75 as determined by WASI
Not Eligible

You will not qualify if you...

  • Suicidality with plan or intent currently or within past 3 months
  • Lifetime history of conduct disorder, autism, any psychotic disorder, or bipolar disorder
  • Eating disorder or alcohol/substance abuse within past 6 months
  • Current treatment or treatment in past 2 years with RF-CBT, CBT, or similar structured therapies
  • Presence of metal braces, retainers, tattoos with metal, or clothing with metal fibers
  • Claustrophobia
  • Current pregnancy or inadequate birth control in sexually active females
  • Use of psychotropic medications other than stable antidepressants
  • Antidepressant dose changes within past 4 weeks or medication changes within past 6 weeks

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Nationwide Children's Hospital

Columbus, Ohio, United States, 43205

Actively Recruiting

2

The Ohio State University

Columbus, Ohio, United States, 43210

Actively Recruiting

3

University of Utah

Salt Lake City, Utah, United States, 84108

Actively Recruiting

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Research Team

S

Scott A Langenecker, Ph.D.

CONTACT

C

Caty Escobar, M.S.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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