Narrative Exposure Therapy in Women With Borderline Personality Disorder and Posttraumatic Stress Disorder

Sponsor
Evangelisches Krankenhaus Bielefeld gGmbH (Other)
Overall Status
Completed
CT.gov ID
NCT02517723
Collaborator
(none)
67
1
2
70
1

Study Details

Study Description

Brief Summary

Narrative Exposure Therapy (NET) is an evidence-based trauma-focussed treatment, suitable for survivors of prolonged and repeated exposure to traumatic stress and childhood adversity. Patients with Borderline Personality Disorder (BPD) often suffer from a comorbid Posttraumatic Stress Disorder (PTSD) caused by multiple traumatic events. Therapeutic aims are the reduction of PTSD-Symptoms in these patients via activation of associative neural networks related to traumatic experiences and habituation of fear and the placement of traumatic experiences in a reconstructed, detailed and consistent autobiography. This practice enables the processing of and coping with painful memories and the construction of clear contingencies of dangerous and safe conditions, generally leading to significant emotional recovery. The investigators assume that using NET the reduction of PTSD symptom severity is greater compared to treatment by Dialectical-Behavioral Therapy (DBT).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Narrative Exposure Therapy
  • Behavioral: Dialectical Behavior Therapy
  • Behavioral: Standard Inpatient Care
  • Other: Waiting List
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
67 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Randomized Controlled Clinical Trial (RCCT) to Test the Effectiveness of Narrative Exposure Therapy (NET) Versus Dialectical-Behavioral Therapy in Reducing Trauma Related Symptoms in Women Suffering From Borderline Personality Disorder (BPD) and Posttraumatic Stress Disorder (PTSD)
Actual Study Start Date :
Apr 1, 2014
Actual Primary Completion Date :
Jan 31, 2020
Actual Study Completion Date :
Jan 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: SIC + NET

Waiting List + Standard Inpatient Care + Narrative Exposure Therapy

Behavioral: Narrative Exposure Therapy
Narrative Exposure Therapy (NET) is based on Testimony Therapy in combination with cognitive behavioural exposure techniques and elements of client-centered counselling. The clients can restore their autobiographic memories about their traumatic experiences. In this way fragmentary memories are transformed into a coherent narrative structure. This practice enables the processing of painful emotions and the construction of clear contingencies of dangerous and safe conditions, generally leading to significant emotional recovery. Therapeutic aims are the reduction of PTSD-Symptomload via activation of fear-network and habituation of fear and the placement of traumatic experiences in a reconstructed, detailed and consistent autobiography. NET will be applied in eight sessions (90-120min/session) in a standardized, manualized manner.
Other Names:
  • NET
  • Behavioral: Standard Inpatient Care
    Unspecific group therapy that is identical in both groups (music therapy etc.)
    Other Names:
  • SIC
  • Other: Waiting List
    Treatment as usual in the community (no DBT, no exposure of trauma memories)

    Active Comparator: SIC + DBT

    Waiting List + Standard Inpatient Care + Dialectical Behavior Therapy

    Behavioral: Dialectical Behavior Therapy
    Dialectical behavior therapy is a cognitive behavioral treatment program developed by Marsha Linehan to treat suicidal clients meeting criteria for BPD. It directly targets suicidal behavior, behaviors that interfere with treatment delivery, and other dangerous, severe, or destabilizing behaviors. Via standard DBT patients improve behavioral capabilities, motivation for skillful behavior, generalization of gains to the natural environment, structuring the treatment environment so that it reinforces functional rather than dysfunctional behaviors. It also targets the therapist capabilities and motivation to treat patients effectively. Patients get weekly individual psychotherapy (1 h/wk), group skills training (3.75 h/wk), a weekly therapist consultation team meetings.
    Other Names:
  • DBT
  • Behavioral: Standard Inpatient Care
    Unspecific group therapy that is identical in both groups (music therapy etc.)
    Other Names:
  • SIC
  • Other: Waiting List
    Treatment as usual in the community (no DBT, no exposure of trauma memories)

    Outcome Measures

    Primary Outcome Measures

    1. Change from first investigation in Posttraumatic Symptom Severity at 18 months (Clinician-Administered PTSD Scale; CAPS) [first investigation (t1), after waiting list (3 months, t2), directly after therapy (3 months, t1), 1 year after therapy (15 months, t3)]

    Secondary Outcome Measures

    1. Change from first investigation in Borderline Symptome Severity at 18 months(Borderline Symptom Liste; BSL) [first investigation (t1), after waiting list (3 months, t2), directly after therapy (6 months, t3), 1 year after therapy (18 months, t4)]

    2. Change from first investigation in Severity of Dissociative Symptoms at 18 months (Fragebogen zu Dissoziativen Symptome ;FDS) [first investigation (t1), after waiting list (3 months, t2), directly after therapy (6 months, t3), 1 year after therapy (18 months, t4)]

    3. Change from first investigation in Severity of Depressive Symptoms at 18 months (Becks Depressions Inventar II, BDI-II) [first investigation (t1), after waiting list (3 months, t2), directly after therapy (6 months, t3), 1 year after therapy (18 months, t4)]

    4. Change from first investigation in Quality of Life at 12 months (WHO-Qualitiy of Life; WHOQOL) [first investigation (t1), after waiting list (3 months, t2), directly after therapy (6 months, t3), 1 year after therapy (18 months, t4)]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • age ≥ 18 years

    • DSM-IV-TR diagnoses of BPD and PTSD

    • legal competence

    • none or stable medication

    • illegal drug abstinence for at least the last 6 months

    • capacity to consent and contract

    Exclusion Criteria:
    • other severe mental disorders (e.g., bipolar disorder, acute psychosis)

    • simultaneous consumption of drugs

    • simultaneous participation in other treatment-studies

    • pregnancy or breastfeeding

    • lack of capability to negotiate a no-suicide agreement

    • suicide attempt or attempts during the 8 weeks prior to start of treatment

    • perpetrator-contact

    • Body Mass Index (BMI) < 16

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Clinic of Psychiatry, Evangelisches Krankenhaus Bielefeld Bielefeld Germany 33617

    Sponsors and Collaborators

    • Evangelisches Krankenhaus Bielefeld gGmbH

    Investigators

    • Study Director: Carolin Steuwe, M.Sc., Clinic of Psychiatry, Evangelisches Krankenhaus Bielefeld
    • Principal Investigator: Martin Driessen, Prof. Dr. med., Clinic of Psychiatry, Evangelisches Krankenhaus Bielefeld

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Prof. Dr. med. Martin Driessen, Martin Driessen, Prof. Dr. med., Evangelisches Krankenhaus Bielefeld gGmbH
    ClinicalTrials.gov Identifier:
    NCT02517723
    Other Study ID Numbers:
    • NET_BPS+PTBS
    First Posted:
    Aug 7, 2015
    Last Update Posted:
    Oct 8, 2021
    Last Verified:
    Oct 1, 2021
    Keywords provided by Prof. Dr. med. Martin Driessen, Martin Driessen, Prof. Dr. med., Evangelisches Krankenhaus Bielefeld gGmbH
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 8, 2021