Emotional Reaction and Self Injury in Patients With Borderline Personality Disorder and Healthy Controls

Sponsor

Katharina Bachmann (Other)

Overall Status

Unknown status

CT.gov ID

NCT03149926

Collaborator

(none)

Enrollment

Location

Anticipated Duration (Months)

7.5

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The current study investigates the emotional response of patients with borderline personality disorder and healthy controls on stimuli associated with self-injury.

Condition or Disease	Intervention/Treatment	Phase
Borderline Personality Disorder Emotions	Other: Stimuli presentation

Study Design

Study Type:

Observational

Anticipated Enrollment :

60 participants

Observational Model:

Other

Time Perspective:

Other

Official Title:

Emotional Reaction of Patients With Borderline Personality Disorder (BPD)on Stimuli Connected to Self-injury - A Comparison Between Patients With BPD and a Healthy Control Group.

Anticipated Study Start Date :

Jun 1, 2017

Anticipated Primary Completion Date :

Dec 1, 2017

Anticipated Study Completion Date :

Feb 1, 2018

Arms and Interventions

Arm	Intervention/Treatment
Patients with Borderline Personality Disorder	Other: Stimuli presentation Different stimuli associated with self-injury are presented. Participants have to rate the emotional effect elected by the stimuli.
Healthy controls	Other: Stimuli presentation Different stimuli associated with self-injury are presented. Participants have to rate the emotional effect elected by the stimuli.

Arm

Intervention/Treatment

Patients with Borderline Personality Disorder

Other: Stimuli presentation

Different stimuli associated with self-injury are presented. Participants have to rate the emotional effect elected by the stimuli.

Healthy controls

Other: Stimuli presentation

Different stimuli associated with self-injury are presented. Participants have to rate the emotional effect elected by the stimuli.

Outcome Measures

Primary Outcome Measures

Emotional reaction [one session of 90min]
Patients comparded to healthy controls will show a stronger emotional reaction on the stimuli. Patients more severely affected will show a stronger emotional reaction compared to less affected patients.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 60 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Patients that are able to use skills and have some therapy experiences.

Exclusion Criteria:

Severe psychiatric comorbidity e.g. psychosis, severe depression, suicidality

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Department of Psychiatry and Psychotherapy - University Hospital, University of Oldenburg	Bad Zwischenahn		Germany	26160

Sponsors and Collaborators

Katharina Bachmann

Investigators

Principal Investigator: Alexandra Philipsen, Prof., Department of Psychiatry and Psychotherapy - University Hospital, University of Oldenburg, Oldenburg, Germany

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Katharina Bachmann, Psychologist Msc., University of Oldenburg

ClinicalTrials.gov Identifier:

NCT03149926

Other Study ID Numbers:

UOldenburg2

First Posted:

May 11, 2017

Last Update Posted:

May 12, 2017

Last Verified:

May 1, 2017

Individual Participant Data (IPD) Sharing Statement:

Undecided

Plan to Share IPD:

Undecided

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Personality Disorders

Borderline Personality Disorder

Self-Injurious Behavior

Study Results

No Results Posted as of May 12, 2017