Does Cognitive Rehabilitation Demonstrate Benefits in the Group Setting With People Whom Have Experienced Brain Injury?
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Purpose
The purpose of this study is to determine whether there is benefit from providing cognitive rehabilitation in the group setting. Several standardized tools will be used to measure progress when a participant enters the group, leaves the group and at a one year follow-up.
| Condition | Intervention |
|---|---|
|
Brain Injuries |
Behavioral: Cognitive Group Therapy |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Efficacy of Group Based Cognitive Rehabilitation Following Acquired Brain Injury |
- provide evidence which supports cognitive therapy in a group setting
- less labor intensive
- cost effectiveness
- peer feedback is effective
| Enrollment: | 20 |
| Study Start Date: | March 2003 |
| Study Completion Date: | March 2008 |
| Primary Completion Date: | February 2007 (Final data collection date for primary outcome measure) |
This research study will look at the outcome benefits of providing cognitive rehabilitation, utilizing the group process. Criteria for selecting the appropriate participants, group format and structure, as well as use of standardized assessments. The assessments used: Three Step Calendar Approach, (Sohlberg and Mateer) Satisfaction With Life scale (SWLS), Community Integration Questionnaire (CIQ), Independent Living Scale, and the Vocational Independence Scale. The group setting provides an atmosphere to work on building communication skills through peer feedback and to develop psychological coping strategies. Techniques such as the problem solving format and a calendar system. Analysis and outcomes of 17 past group participants were analyzed supporting cognitive rehabilitation in the group setting.
Of the 20 participants, 3 chose not to be included.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- All participants involved in the Cognitive Rehabilitation Outpatient Group within the study time frame are eligible to be in the study.
Contacts and Locations| United States, Minnesota | |
| Mayo Clinic | |
| Rochester, Minnesota, United States, 55905 | |
| Principal Investigator: | Merri L Vitse | Mayo Clinic |
More Information
No publications provided
| Responsible Party: | Merri L Vitse, AS, Mayo Clinic |
| ClinicalTrials.gov Identifier: | NCT00166348 History of Changes |
| Other Study ID Numbers: | 1069-03 |
| Study First Received: | September 12, 2005 |
| Last Updated: | January 19, 2010 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Mayo Clinic:
|
Cognitive Rehabilitation |
Additional relevant MeSH terms:
|
Brain Injuries Brain Diseases Central Nervous System Diseases Nervous System Diseases |
Craniocerebral Trauma Trauma, Nervous System Wounds and Injuries |
ClinicalTrials.gov processed this record on May 22, 2013