- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00567242
Treating Intention In Aphasia: Neuroplastic Substrates
April 30, 2012 updated by: University of Florida
The purpose of this study is to determine if an "intentional act" improves treatment response for patients with nonfluent aphasia.
The treatment involves naming pictures and saying members of categories.
The "intentional act" requires initiating picture naming or category member trials with a left-hand movement sequence.
Nonfluent aphasia is a disorder of language production in which patients with damage to the brain's language system have trouble initiating and maintaining spoken communication.
All patients participating in the study take part in functional MRI scans to determine how treatments affect brain systems.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A new treatment manipulating intention substrates for language production in "nonfluent" aphasia patients was developed.
The intention component involves initiating word-finding trials with a complex left-hand movement.
The study addresses (1) whether or not the intention manipulation (complex left-hand movement) makes a unique contribution to treatment outcome and (2) whether or not the intention manipulation helps to shift word production mechanisms from the left to the right frontal lobe.
All study participants take part in functional magnetic resonance imaging (fMRI) scans of word-finding before and after treatment and at 3-month follow-up to measure changes in lateralization of frontal lobe activity during word finding.
Only patients with a substantial degree of left frontal activity on the pre-treatment fMRI scan can participate.
There are three specific aims: (1) to determine if repetitive initiation of word production with a complex left-hand movement leads to increased right-hemisphere lateralization of frontal activity and if these changes can be attributed to the intention component of treatment, (2) to determine whether activity in posterior perisylvian cortices that is entrained to right frontal activity shows a greater increase in right-hemisphere lateralization from pre- to post-treatment fMRI when the intention component is included in treatment, and (3) to determine whether onset of hemodynamic responses (HDRs) in right motor/premotor cortex becomes more closely associated with the temporal onset of participants' spoken responses across treatment when the intention component is included in treatment.
If successful, the treatment can provide a new treatment vehicle for increasing language function in patients with "nonfluent" aphasia.
Study Type
Interventional
Enrollment (Actual)
14
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Florida
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Gainesville, Florida, United States, 32610
- University of Florida
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Jacksonville, Florida, United States, 32216
- Brooks Center for Rehabilitation Studies
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Jacksonville, Florida, United States, 32209
- University of Florida/Shands Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 95 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Nonfluent aphasia caused by stroke
- Moderate to severe word-finding problems
- 6 or more months post stroke
- Right handed prior to stroke
- All strokes in left hemisphere
- Native English speaker
- Capable of following verbal directions
Exclusion Criteria:
- Severe impairment of word comprehension
- Brain injury or disease in addition to stroke
- Drug or alcohol abuse within past 6 months
- Schizophrenia or other psychiatric disorder necessitating hospitalization
- History of learning disability
- Claustrophobia
- Cardiac pace-maker
- Ferrous metal implants not attached to bone, metal fragments in body
- Profound hearing loss
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Word-finding with intention component
Treats word-finding (picture naming, category member generation) with an intention manipulation (complex left-hand movement to initiate word-finding trials)
|
Word-finding trials (picture-naming) with intention manipulation (initiating word-finding trials with a complex left-hand movement).
8 (or more) baseline sessions over 4 days followed by 30 treatment sessions (2 sessions/day, 5 days/week for 3 weeks).
Other Names:
|
|
Active Comparator: Word-finding with no intention component
Word-finding trials similar to intention mediated treatment, but without intention manipulation
|
Word-finding trials with no intention manipulation.
8 (or more) baseline sessions in 4 days followed by 30 treatment sessions (2 sessions/day, 5 days/week for 3 weeks).
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lateralization of Frontal Lobe (and Posterior Perisylvian) Activity During Word Production
Time Frame: immediately post-treatment scan minus pre-treatment baseline scan
|
Functional MRI laterality indices (LIs)were calculated for lateral frontal, medial frontal, and posterior perisylvian cortex regions of interest (ROIs): L=number of active voxels in left hemisphere ROI and R=number of active voxels in right hemisphere ROI using the following formula: (L-R)/(L+R).
LIs could vary from -1 (completely right lateralized) to +1 (completely left lateralized).
Then, change in LIs was calculated by subtracting the pre-treatment from the post-treatment and 3-mo follow-up LI.
It was expected the intention manipulation would show a rightward shift in LI.
|
immediately post-treatment scan minus pre-treatment baseline scan
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Picture Naming Probe Scores (% Accuracy)
Time Frame: trend for time series of 8 baseline + 30 treatment sessions
|
Improvement for the time series from 8 baseline sessions through 30 treatment sessions for naming probes was computed with the C statistic using Tryon's (1982, 1983) formula for each subject.
C statistics were converted to Z scores, using the formula provided by Tryon (1982).
Z scores indicated treatment change for each subject, with a positive and significant Z score indicating substantive treatment gains.
Z scores were then compared between groups with a t statistic.
It was expected that the intention manipulation would lead to greater treatment gains than when it was not used.
|
trend for time series of 8 baseline + 30 treatment sessions
|
|
Category Member Generation Probe Scores (% Accuracy)
Time Frame: trend for time series of 8 baseline + 30 treatment sessions
|
Improvement for the time series from 8 baseline sessions through 30 treatment sessions for naming probes was computed with the C statistic using Tryon's (1982, 1983) formula for each subject.
C statistics were converted to Z scores, using the formula provided by Tryon (1982).
Z scores indicated treatment change for each subject, with a positive and significant Z score indicating substantive treatment gains.
Z scores were then compared between groups with a t statistic.
It was expected that the intention manipulation would lead to greater treatment gains than when it was not used.
|
trend for time series of 8 baseline + 30 treatment sessions
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Bruce Crosson, PhD, University of Florida
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Crosson B, Fabrizio KS, Singletary F, Cato MA, Wierenga CE, Parkinson RB, Sherod ME, Moore AB, Ciampitti M, Holiway B, Leon S, Rodriguez A, Kendall DL, Levy IF, Rothi LJ. Treatment of naming in nonfluent aphasia through manipulation of intention and attention: a phase 1 comparison of two novel treatments. J Int Neuropsychol Soc. 2007 Jul;13(4):582-94. doi: 10.1017/S1355617707070737. Epub 2007 May 18.
- Crosson B, McGregor K, Gopinath KS, Conway TW, Benjamin M, Chang YL, Moore AB, Raymer AM, Briggs RW, Sherod MG, Wierenga CE, White KD. Functional MRI of language in aphasia: a review of the literature and the methodological challenges. Neuropsychol Rev. 2007 Jun;17(2):157-77. doi: 10.1007/s11065-007-9024-z. Epub 2007 May 25.
- Gopinath K, Crosson B, McGregor K, Peck K, Chang YL, Moore A, Sherod M, Cavanagh C, Wabnitz A, Wierenga C, White K, Cheshkov S, Krishnamurthy V, Briggs RW. Selective detrending method for reducing task-correlated motion artifact during speech in event-related FMRI. Hum Brain Mapp. 2009 Apr;30(4):1105-19. doi: 10.1002/hbm.20572.
- Conway T, Heilman KM, Gopinath K, Peck K, Bauer R, Briggs RW, Torgesen JK, Crosson B. Neural substrates related to auditory working memory comparisons in dyslexia: an fMRI study. J Int Neuropsychol Soc. 2008 Jul;14(4):629-39. doi: 10.1017/S1355617708080867.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2007
Primary Completion (Actual)
September 1, 2009
Study Completion (Actual)
September 1, 2009
Study Registration Dates
First Submitted
November 30, 2007
First Submitted That Met QC Criteria
November 30, 2007
First Posted (Estimate)
December 4, 2007
Study Record Updates
Last Update Posted (Estimate)
May 3, 2012
Last Update Submitted That Met QC Criteria
April 30, 2012
Last Verified
April 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01DC007387-01A1 (U.S. NIH Grant/Contract)
- R01DC007387 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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