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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01573689
Other study ID # VLeblanc - bereaved children
Secondary ID
Status Completed
Phase N/A
First received April 5, 2012
Last updated May 7, 2013
Start date September 2012
Est. completion date November 2012

Study information

Verified date May 2013
Source Université de Montréal
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The methodology of this clinical trial is based on the realisation of a group intervention with children who lost a parent. Interviews preintervention and postintervention with participants will be done as well. The purpose of this study is to answer the following question: "What are the benefits for children who are in the process of bereaving a parent to participate in a group work intervention based on the mutual aid model ?". The aim of the research is to explore the benefits for grieving children to participate in an group work intervention based on the mutual aid model. To do so, the research has three distinct objectives : 1) to develop and apply a program of group work interventions for grieving children based on the mutual aid model ; 2) to explore the extent to which participation in the group facilitates changes in the children's discourse about death and the loss of their parents, and 3) to examine, from the children's own perceptive, the possible impact that their participation in the group have on their experience of bereavement.


Recruitment information / eligibility

Status Completed
Enrollment 4
Est. completion date November 2012
Est. primary completion date November 2012
Accepts healthy volunteers No
Gender Both
Age group 8 Years to 12 Years
Eligibility Inclusion Criteria:

- Children between 8 and 12 years old.

- Children who had lost a parent within 3 months and two years before the beginning of the group intervention.

Exclusion Criteria:

- Children who experimented death of his parent by suicide.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Behavioral:
Group intervention based on mutual aid.
Development of a mutual aid group and his actualization on children between nine and twelve years old who had lost one of their parents.

Locations

Country Name City State
Canada Lumi-Vie Laval Quebec

Sponsors (1)

Lead Sponsor Collaborator
Université de Montréal

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mutual aid group intervention A mutual aid group intervention has been develop to help children who had lost a parent. The activities are based on the theoretical knowledge and needs of grieving children. 8 weeks No
Secondary Interview before the group intervention The interview aim is to know and to understand the experience of each participant about the death of their parent. one of 60 minutes No
Secondary Interview after the group intervention The aim of this interview is to ask questions about the death and the experience of the children after the end of the group intervention. Through the answers, we will find out about to understanding and the perceptions of the children about the group intervention. One of 60 minutes No