Does Cognitive Rehabilitation Demonstrate Benefits in the Group Setting With People Whom Have Experienced Brain Injury?
Efficacy of Group Based Cognitive Rehabilitation Following Acquired Brain Injury
1 other identifier
interventional
20
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2003
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2003
CompletedFirst Submitted
Initial submission to the registry
September 12, 2005
CompletedFirst Posted
Study publicly available on registry
September 14, 2005
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2008
CompletedJanuary 20, 2010
January 1, 2010
3.9 years
September 12, 2005
January 19, 2010
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
provide evidence which supports cognitive therapy in a group setting
less labor intensive
cost effectiveness
peer feedback is effective
Interventions
Eligibility Criteria
You may qualify if:
- All participants involved in the Cognitive Rehabilitation Outpatient Group within the study time frame are eligible to be in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Mayo Cliniclead
- Nicloe Holzworth, OTR/Lcollaborator
- Bergequist, Thomas, Ph.D.collaborator
- Brown, Allen, M.D.collaborator
- Sue Lepore, OTR/Lcollaborator
- Walter Stobaugh. LICSWcollaborator
Study Sites (1)
Mayo Clinic
Rochester, Minnesota, 55905, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Merri L Vitse
Mayo Clinic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 12, 2005
First Posted
September 14, 2005
Study Start
March 1, 2003
Primary Completion
February 1, 2007
Study Completion
March 1, 2008
Last Updated
January 20, 2010
Record last verified: 2010-01