NCT00447252

Brief Summary

The present study will focus on several objectives in the framework of the family perspective and systemic understanding of the mourning process:

  1. 1.Identification of the psychological, social and practical needs of families that have lost a child to terrorism.
  2. 2.Deepening and extending the knowledge of how families cope with the loss of a child in a violent incident of a security-related nature.
  3. 3.Identification of risk and resilience factors within the family structure, and the nature of the relationships within the family.

Trial Health

55
Monitor

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

January 1, 2007

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 13, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 14, 2007

Completed
Last Updated

March 14, 2007

Status Verified

March 1, 2007

First QC Date

March 13, 2007

Last Update Submit

March 13, 2007

Conditions

Bereaved Families

Keywords

bereavementgrief

Eligibility Criteria

Age2 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • lost a son or daughter below the age of 18 as a result of a terrorist incident,
  • at least six months previously

You may not qualify if:

  • single-parent families
  • family members who suffer from mental retardation, disturbances because of addiction, or psychiatric disturbance from the psychotic or autistic spectra (schizophrenia, manic-depressive illness, psychotic disturbances, PDD).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Israel Center for the Treatment of Psychotrauma

Jerusalem, Israel

RECRUITING

Study Officials

  • Danny Brom, Ph.D

    The Israel Center for the Treatment of Psychotrauma

    STUDY DIRECTOR

Central Study Contacts

Danny Brom, Ph.d

CONTACT

+972-2-6449666dbrom@herzoghospital.org

Study Design

Study Type
observational
Observational Model
DEFINED POPULATION
Time Perspective
OTHER
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 13, 2007

First Posted

March 14, 2007

Study Start

January 1, 2007

Last Updated

March 14, 2007

Record last verified: 2007-03

Locations

IL(1)