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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03018639
Other study ID # DBT_dropout
Secondary ID
Status Completed
Phase N/A
First received January 9, 2017
Last updated January 11, 2017
Start date December 2012
Est. completion date August 2016

Study information

Verified date January 2017
Source Evangelisches Krankenhaus Bielefeld gGmbH
Contact n/a
Is FDA regulated No
Health authority Ethics Commission: Ethikkommission der Ärztekammer Westfalen-Lippe
Study type Observational

Clinical Trial Summary

Participants with Borderline pathology (≥ 3 DSM-IV-criteria) receiving an inpatient Dialectical Behavior Therapy (DBT) program completed a quality assurance questionnaire set assessing demographic information and pretreatment psychopathology during the days of their inpatient stay. Beyond that, changes of therapists were documented.


Recruitment information / eligibility

Status Completed
Enrollment 89
Est. completion date August 2016
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- three or more criteria for BPD as defined by DSM-IV (Borderline Personality characteristics; BPC)

Exclusion Criteria:

- inability to contract and consent,

- other severe mental disorders (bipolar disorder, acute psychosis),

- current alcohol,

- illicit or not prescribed drug use,

- simultaneous participation in other treatment studies,

- pregnancy or breastfeeding,

- an inability to negotiate a non-suicide agreement,

- ongoing traumatic contact with the perpetrator, and

- a Body Mass Index < 16.5.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Intervention

Behavioral:
Dialectical Behavior Therapy
DBT is a cognitive-behavioral treatment program that was developed to treat suicidal Patients with BPD (Linehan, 1993).

Locations

Country Name City State
Germany Research Department Bielefeld

Sponsors (1)

Lead Sponsor Collaborator
Evangelisches Krankenhaus Bielefeld gGmbH

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dropout 10 weeks No
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