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Clinical Trials/NCT02397187
NCT02397187
Unknown
Not Applicable

The Assessment of the Efficacy of a Structured, Dimension-based, STI (Short Term Intervention) in De-compensated Personality-disorder, Hospitalized, Patients

Shalvata Mental Health Center0 sites20 target enrollmentMarch 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Personality Disorders
Sponsor
Shalvata Mental Health Center
Enrollment
20
Primary Endpoint
Questionnaires
Last Updated
11 years ago

Overview

Brief Summary

The assessment of the efficacy of a structured, dimension-based, STI (Short Term Intervention) in de-compensated Personality-disorder, hospitalized, patients

Detailed Description

The current study attempts to design a short-term intervention aimed at stabilizing decompensate personality disorder patients in hospitalization. The study is structured as a pilot study, thus will enroll 20 patients only. Patients, upon being hospitalized and after signing the consent to participate in the study, will be randomized to two groups: The first will be treated by the novel, LOOP, concept' the other will be TAU, as routinely done with PersDis patients in the investigators facility. The outcome parameters will be changes in series of questionnaires filled upon being enrolled and at the end of the intervention. Another outcome parameter will be readmission rates in the post-intervention period (3 months). The LOOP conceptualizes the psyche by a three-dimension structure: the space (the potential of experiencing, the "place" where the investigators experiences occur), the content (the experiences themselves; action, thoughts, feelings, experiences and being) and the order (the relationship between the various contents). The LOOP intervene with these three dimensions by a structures scheme, aimed at allowing the patient to quickly reclaim the responsibility on his psyche, stabilize and initiate long-term rehabilitation processes.

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
March 2016
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Cluster 2 diagnosis
  • No suicide attemts 1 month prior to admission
  • Regularly treated
  • An active support system
  • No urgent need for Rx changes

Exclusion Criteria

  • Drug abuse
  • An active Axis 1 diagnosis that requires change in Rx
  • Unable to read/write fluently

Outcomes

Primary Outcomes

Questionnaires

Time Frame: up to 28 days

Questionnaires filled upon being enrolled and at the end of the intervention

Readmission rates

Time Frame: 3 months

Readmission rates in the post-intervention period (3 months).

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