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Outcome of Crisis Intervention for Subjects With Borderline Personality Disorder or Post-Traumatic Stress Disorder

Study of Outcome With an Intervention From the Cape Cod Model of Psychotherapy for Subjects in a Behavioral Crisis and With the Diagnosis of Borderline Personality Disorder (BPD) or Post-Traumatic Stress Disorder (PTSD)

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00269139
Enrollment
40
Registered
2005-12-23
Start date
Unknown
Completion date
Unknown
Last updated
2006-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Borderline Personality Disorder, Post-Traumatic Stress Disorders

Keywords

Behavioral crisis, Perception of social crisis, Repetition compulsion, Intrusive mental events, Uncontrollable urges

Brief summary

Dr. Laddis will test a hypothesis about the nature and the management of behavioral crises in patients with borderline personality disorder (BPD) or post-traumatic stress disorder (PTSD). The term behavioral crisis is used strictly for periods of uncontrollable urges to repeat mental or outward activity, e.g., flashbacks, cutting, binging on food, drugs or sex, with no intervals to rethink one's priorities or to consider others' direction. The clinical hypothesis states, in two steps, that: 1. the perception of a life crisis precedes and then underlies every behavioral crisis; 2. the behavioral crisis resolves promptly and all symptoms end if the clinicians engage the patient about his management of the life crisis that underlies the symptoms.

Detailed description

Subjects in the experimental group will be treated by Dr. Laddis after their admission to a crisis stabilization unit (CSU) or to an inpatient unit (IPU) for a behavioral crisis. Subjects will be included at random, as assigned to Dr. Laddis according to his routine duties at those units. Subjects in the control group will receive treatment for behavioral crisis according to the preference of the clinical staff at other comparable units. That treatment will constitute treatment as usual. Clinicians in the control settings will not be informed about the experimental hypothesis, the clinical intervention and the contingent outcomes. The subjects will be tested for the results of treatment 12-24 hours after composition of a treatment plan. The testing will be done with the Brief Psychiatric Rating Scale (BPRS), as well as with a set of criteria devised by Dr. Laddis to measure the outward behavior and the mental events during behavioral crisis. The patients and the attending frontline staff will be interviewed also about their beliefs in regard to what, among the clinicians' interventions, made a difference for the course of the behavioral crisis, for better or for worse. The raters will be trained for interrater reliability and they will not be informed about the hypothesis.

Interventions

BEHAVIORALCrisis resolution

Sponsors

Laddis, Andreas, M.D.
Lead SponsorINDIV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed with BPD or PTSD, with a structured interview according to the current diagnostic manual * In behavioral crisis

Exclusion criteria

* Brain damage * Currently intoxicated with alcohol or drugs or in withdrawal

Design outcomes

Primary

MeasureTime frame
Brief Psychiatric Rating Scale (BPRS) scores
Scores on Client Observation and Client Interview, tools designed for this study

Secondary

MeasureTime frame
Patient interview and ratings for the value of the clinicians' interventions
Staff interview and ratings for their own interventions

Countries

United States

Contacts

Primary ContactAndreas Laddis, MD
andreas.laddis@dmh.state.ma.us508-320-7895

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026