Affect Management Group for Adult Survivors of Childhood Trauma

NCT ID: NCT00383006

Last Updated: 2009-06-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

PHASE1

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-05-31

Study Completion Date

2008-05-31

Brief Summary

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Problems of self regulation, e.g. emotional dysfunction, represent a core symptom of adult patients with traumatic childhood experiences. The study intends to evaluate the efficiency of a 14-week group therapy for adult survivors of relational trauma in childhood. Main interventions are psychoeducation about the sequelae of childhood trauma, teaching of skills for affect regulation and techniques for activating resources. The hypothesis is that the group therapy significantly improves the participant's capacity in emotion management and self-soothing.

Detailed Description

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Problems of self regulation, e.g. emotional dysfunction, represent a core symptom of adult patients with traumatic childhood experiences. Since sufficient capacity for self soothing and emotional regulation are essential for trauma exposure, modern trauma therapy concepts are phase-oriented, beginning with working on "stabilization". The study intends to evaluate the efficiency of a 14-week group therapy for adult survivors of relational trauma in childhood. Main interventions are psychoeducation about the sequelae of childhood trauma, teaching of skills for affect regulation and techniques for activating resources. Inclusion criteria are clinical significant problems with self-regulation and the presence of childhood trauma. Outcome measures are based on self-rating questionnaires, clinical interviews and an experimental computer-task at timepoint pre-, post- and 3-month-follow-up. There is no control condition in the pilot-study phase.

Conditions

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Stress Disorders, Post-Traumatic

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Skills for affect regulation (behavior)

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Adults with moderate to severe relational trauma in childhood (emotional, sexual or physical abuse, emotional or physical neglect)
* DSM-IV diagnosis of posttraumatic stress disorder

Exclusion Criteria

* Severe dissociation
* Environmental safety problems
* Ongoing enmeshment with perpetrators
* Psychotic disorders
* Severe depression
* Acute suicidality
* Substance abuse
* Severe cognitive decline
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Zurich

OTHER

Sponsor Role lead

Principal Investigators

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Christoph Mueller, MD

Role: PRINCIPAL_INVESTIGATOR

Department of Psychiatry, University Hospital, 8091 Zurich, Switzerland

Michael Rufer, MD

Role: PRINCIPAL_INVESTIGATOR

Department of Psychiatry, University Hospital, 8091 Zurich, Switzerland

Locations

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Department of Psychiatry, University Hospital

Zurich, Canton of Zurich, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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PSYUNIZH26092006

Identifier Type: -

Identifier Source: org_study_id

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