NCT00463138

Brief Summary

Researchers examined perceived satisfaction and perceived increase or decrease in symptoms among recipients of treatment at the Jerusalem Center for the Treatment of Psychotrauma, using self report methods. Researchers hypothesized that a significant number of recipients would report a decrease in their symptoms and general satisfaction with the treatment they received.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Apr 2007

Shorter than P25 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2007

Completed
18 days until next milestone

First Submitted

Initial submission to the registry

April 19, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

April 20, 2007

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2008

Completed
Last Updated

September 4, 2013

Status Verified

September 1, 2013

Enrollment Period

11 months

First QC Date

April 19, 2007

Last Update Submit

September 3, 2013

Conditions

Healthy

Keywords

perceived increase or decrease in symptoms post treatmentSatisfaction with the treatment

Outcome Measures

Primary Outcomes (1)

  • depressive symptoms, anxiety, PDS, which measures subjective response to trauma, symptoms, and and level of functioning.

    April 2007- March 2008

Secondary Outcomes (1)

  • level of family, friend, and other support, Self-Efficacy Scale

    Aprol 2007- March2008

Other Outcomes (1)

  • Traumatic Events Screening Inventory (TESI)

    April 2008- March 2008

Interventions

Crisis interventionBEHAVIORAL

Eligibility Criteria

Age12 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

All clients who were exposed to a traumatic event within the last 2 years and completed treatment at the Trauma Center within the last year

You may qualify if:

  • All clients who were exposed to a traumatic event within the last 2 years and completed treatment at the Trauma Center within the last year

You may not qualify if:

  • Clients under the age of 12

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Crisis Intervention

Intervention Hierarchy (Ancestors)

PsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Danny Brom, Ph.D

    Israel Center for the Treatment of Psychotrauma

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research director

Study Record Dates

First Submitted

April 19, 2007

First Posted

April 20, 2007

Study Start

April 1, 2007

Primary Completion

March 1, 2008

Study Completion

March 1, 2008

Last Updated

September 4, 2013

Record last verified: 2013-09