Family Involvement in The Treatment Of a Mentally Ill Relative

Not Applicable

• Conditions: Families of Mentally Ill

• Registration Number: NCT00258167
• Lead Sponsor: Lev-Hasharon Mental Healtlh Center

Brief Summary

* Research demonstrates that the families of the seriously mentally ill are burdened by this caregiving role and by their responsibilities

* Research also demonstrates that family interventions are effective and that they have a potential to reduce family burden, as well as to improve the condition of the mentally ill patients.

* We assume that the sibling group intervention would be effective in reducing the family burden of the siblings, and that this reduction would be reflected in their replies to the "Experience of Caregiving Inventory".

Detailed Description

* The group for siblings is an intervention which is carried out in the outpatient clinic of Lev HaSharon Mental Health Center in cycles which last eight weeks;

* Every group cycle will include between 10-14 participants, all siblings of persons with mental illness. The patients themselves (ill siblings) are either hospitalized in Lev HaSharon Mental Health Center, or are outpatients in the Lev HaSharon Mental Health Outpatient Unit, or in the community at large.

* The group is an ongoing group: short term intensive group intervention in a dynamic orientation. Veteran participants of each cycle are welcome to re-join at following cycles, and at the same time new participants can join at the beginning of each cycle.

* Participants will be asked to fill the "Experience of Caregiving Inventory" twice: first time before the first meeting of a particular cycle of sibling group and second time: after the last (eighth) meeting of this group cycle.

Study Timeline

• Study Start: 2005-11
• Study First Submitted: 2005-11-23
• Study First Submitted QC: 2005-11-23
• Study First Posted: 2005-11-24
• Status Verified: 2008-06
• Last Update Submitted: 2008-06-10
• Last Update Posted: 2008-06-11
• Primary Completion: 2008-11
• Study Completion: 2008-11

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• siblings of persons with mental illness

Exclusion Criteria

• persons junior then 18 years old

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Score on the "Experience of Caregiving Inventory" following 8 weeks of participation in the group.	8 weeks

Trial Locations

Locations (1)

Lev-HasharonMHC; 🇮🇱 Netanya, Israel