Family Involvement in The Treatment Of a Mentally Ill Relative
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00258167|
Recruitment Status : Unknown
Verified June 2008 by Lev-Hasharon Mental Healtlh Center.
Recruitment status was: Recruiting
First Posted : November 24, 2005
Last Update Posted : June 11, 2008
- 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".
|Condition or disease||Intervention/treatment||Phase|
|Families of Mentally Ill||Behavioral: filling the "Experience of Caregiving Inventory"||Not Applicable|
- 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 Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||50 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Family Involvement in The Treatment Of a Mentally Ill Relative|
|Study Start Date :||November 2005|
|Estimated Primary Completion Date :||November 2008|
|Estimated Study Completion Date :||November 2008|
Behavioral: filling the "Experience of Caregiving Inventory"
- Score on the "Experience of Caregiving Inventory" following 8 weeks of participation in the group. [ Time Frame: 8 weeks ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00258167
|Contact: Igor Oyffe, MDemail@example.com|
|Netanya, Israel, 42100|
|Contact: Igor Oyffe, MD 972-9-8981248 firstname.lastname@example.org|
|Contact: Shuvit Melamed, MSW +972-9-8981278 email@example.com|
|Principal Investigator: Igor Oyffe, MD|
|Sub-Investigator: Shuvit Melamed, MSW|
|Sub-Investigator: Michal Ferkel, MSW|
|Principal Investigator:||Igor Oyffe, MD||Lev-Hasharon Mental Healtlh Center|