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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01343550
Other study ID # PHS6019
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date February 2011
Est. completion date August 2011

Study information

Verified date February 2011
Source State University of New York - Upstate Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that a creativity skills group for Borderline Personality Disorder can reduce symptoms of BPD, depression, and anxiety.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 2011
Est. primary completion date August 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18 years of age or older - participant self-reports clinical diagnosis of Borderline Personality Disorder - currently seeing an individual therapist on a regular basis

Study Design


Intervention

Other:
creativity group
This is a creativity group intervention. There will be 4 groups. Each group has one session per week. Each session is a duration of two hours.

Locations

Country Name City State
United States SUNY Upstate Medical University Syracuse New York

Sponsors (1)

Lead Sponsor Collaborator
State University of New York - Upstate Medical University

Country where clinical trial is conducted

United States, 

References & Publications (2)

Gunderson JG. Borderline personality disorder: ontogeny of a diagnosis. Am J Psychiatry. 2009 May;166(5):530-9. doi: 10.1176/appi.ajp.2009.08121825. Review. — View Citation

Jacob GA, Gabriel S, Roepke S, Stoffers JM, Lieb K, Lammers CH. Group therapy module to enhance self-esteem in patients with borderline personality disorder: a pilot study. Int J Group Psychother. 2010;60(3):373-87. doi: 10.1521/ijgp.2010.60.3.373. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Borderline Evaluation of Severity Over Time (BEST) baseline, 5th week, post-intervention (week 8)
Secondary Beck Depression Inventory (BDI) baseline, week 5, week 8
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