A Study to Determine Whether Ongoing Assessment Aids Treatment

Overview

About this study

The purposes of this study are to summarize clinician evaluations of the NNDC battery in the single clinic where the adult battery is currently being administered to adolescents, to determine patient and clinician level of interest in using the NNDC battery in clinics where the adult battery is not currently being administered to adolescent patients (n=14), to measure change in evaluation 3 months post-implementation for any sites that begin administering the NNDC battery to adolescents, and to generate potential new Child and Adolescent Mood Disorders Interest Group (CAMDIG) research protocols for future consideration.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Children and adolescents ages 12-17 years old.
  • Diagnoses of any depressive or bipolar disorder.
  • Ability to read the questionnaire.

Exclusion Criteria:

  • Inability to speak English.

 

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Jarrod Leffler, Ph.D., L.P.

Closed for enrollment

Contact information:

Cynthia Stoppel CCRP

(507)284-5914

Stoppel.Cynthia@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20467304

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