Promoting Recovery Processes in Women With Borderline Personality Disorder Using a Dynamic Cognitive Intervention
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|ClinicalTrials.gov Identifier: NCT01531634|
Recruitment Status : Unknown
Verified February 2012 by Hillel Yaffe Medical Center.
Recruitment status was: Not yet recruiting
First Posted : February 13, 2012
Last Update Posted : February 13, 2012
The field of psychiatric rehabilitation focuses on creating a personal narrative and developing coping strategies and environmental supports. The concept of recovery is person-centered and emphasizes the person's ability to change and to live meaningful life. The strengths approach has a central role in the recovery concept, emphasizing the person's abilities and potential. A preserved cognitive ability can be a significant strength in the recovery process.
Research had shown growing support for the use of cognitive-behavioral approaches as the most effective therapy for people with borderline personality disorder, using structured interventions. A central focus in cognitive therapy is the change of maladaptive schemes. The dynamic-cognitive intervention (DCI) is based on the understanding of structural cognitive modifiability and suggests the use of mediated learning in order to enhance sense of competence and develop better psychological coping skills.
The present study will focus on women diagnosed with borderline personality disorder, with normative cognitive ability seen as a strength as opposed to their emotional ability. This study will examine the effects of a Dynamic Cognitive Intervention on recovery measures and on symptoms severity.
The study will include 30 women aged 18-45 years. Participants will be randomly assigned to an intervention group and a control group. All participants will be assessed before and after intervention using Recovery Assessment Scale, Hope Scale and The Brief Symptom Inventory.
The intervention designed for this study is based on the principles of the Dynamic Cognitive Intervention. The intervention tools that will be used include: a. Instrumental Enrichment tools. b. life events analysis. c. Stories, lyrics and movie clips. d. Worksheets. The intervention encompasses 12 sessions of 1.5 hours, with a routine structure.
The results are expected to contribute to the understanding of the impact of a dynamic cognitive intervention in women diagnosed with borderline personality disorder.
|Condition or disease||Intervention/treatment|
|Borderline Personality Disorder||Behavioral: Dynamic Cognitive Intervention Group|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||30 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Promoting Recovery Processes in Women Diagnosed With Borderline Personality Disorder Using a Dynamic Cognitive Intervention|
Active Comparator: Dynamic Cognitive Intervention Group
Twelve Meetings of Dynamic Cognitive Intervention.
Behavioral: Dynamic Cognitive Intervention Group
Twelve meetings of a Dynamic Cognitive Intervention group.
Other Name: DCI
|No Intervention: No Additional Intervention|
- Change in Recovery Assessment Scale [ Time Frame: Change from baseline in Recovery Assessment Scale at 12th meeting (6 up to 12 weeks) ]A baseline Recovery Assessment Scale will be used on the first intervention group meeting. Recovery Assessment Scale will be used again on the last (i.e. 12th) intervention group meeting.
- Change in Hope Scale [ Time Frame: Change from baseline in Hope Scale at 12th meeting (6 up to 12 weeks) ]A baseline Hope Scale will be used on the first intervention group meeting. Hope Scale will be used again on the last (i.e. 12th) intervention group meeting.
- Change in Brief Symptom Inventory [ Time Frame: Change from baseline in Brief Symptom Inventory at 12th meeting (6 up to 12 weeks) ]A baseline Brief Symptom Inventory will be used on the first intervention group meeting. Brief Symptom Inventory will be used again on the last (i.e. 12th) intervention group meeting.
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): NCT01531634
|Contact: Orly Tsabar, B.O.T.||firstname.lastname@example.org|
|Day Center for Mentally Ill||Not yet recruiting|
|Principal Investigator: Orly Tsabar, B.O.T.|
|Principal Investigator:||Orly Tsabar, B.O.T.||Tel Aviv University|