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Treatment for Word Retrieval Impairments in Aphasia

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2012 by Dr. Anastasia Raymer, Old Dominion University.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00764400
First Posted: October 2, 2008
Last Update Posted: May 21, 2012
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.
Collaborator:
National Institute on Deafness and Other Communication Disorders (NIDCD)
Information provided by (Responsible Party):
Dr. Anastasia Raymer, Old Dominion University
September 30, 2008
October 2, 2008
May 21, 2012
August 2008
June 2012   (Final data collection date for primary outcome measure)
Daily Probe Picture Naming [ Time Frame: daily probes from three times per week for up to 3 months and one month posttreatment ]
Daily Probe Picture Naming [ Time Frame: daily probes from pretreatment to one month posttreatment ]
Complete list of historical versions of study NCT00764400 on ClinicalTrials.gov Archive Site
  • Western Aphasia Battery [ Time Frame: pre-treatment and at treatment completion ]
  • Boston Naming Test [ Time Frame: pretreatment and at treatment completion ]
  • Discourse Sample [ Time Frame: pre-treatment and at treatment completion ]
  • Western Aphasia Battery [ Time Frame: pre- and post-treatment ]
  • Boston Naming Test [ Time Frame: pre- and post-treatment ]
  • Discourse Sample [ Time Frame: pre- and post-treatment ]
  • Communicative Effectiveness Index [ Time Frame: pre- and post-treatment ]
  • Functional Outcomes Questionnaire for Aphasia [ Time Frame: pre- and post-treatment ]
Not Provided
Not Provided
 
Treatment for Word Retrieval Impairments in Aphasia
Communication Outcomes for Naming Treatments in Aphasia
In this study the investigators are examining the effectiveness of two different speech therapy protocols for word retrieval impairments experienced by individuals with stroke-induced aphasia. One treatment involves errorless naming treatment and the other employs verbal plus gestural facilitation of word retrieval. Participants will receive one of the two treatments over several months. Before and after treatment the investigators will administer several tests and conversational samples to examine changes associated with the treatments. The investigators hypothesize that, whereas both treatments will lead to improvements in words rehearsed in therapy, communication outcomes in conversation will be broader for the verbal plus gestural protocol.
Not Provided
Interventional
Phase 1
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Investigator)
Primary Purpose: Treatment
Stroke
Behavioral: Word Retrieval Treatments for Aphasia
Speech therapy sessions take place 4 times per week for up to 90 minutes per session. Following a phase of baseline pre-testing, two phases of speech therapy will take place lasting up to 20 sessions per phase. Post-testing will take place immediately upon completion of the treatment phases and again at 1 month post study completion.
  • Experimental: Errorless Naming Treatment
    Intervention: Behavioral: Word Retrieval Treatments for Aphasia
  • Experimental: Verbal+Gestural Facilitation
    Intervention: Behavioral: Word Retrieval Treatments for Aphasia
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
16
July 2012
June 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • left hemisphere stroke >4 months earlier
  • aphasia with word retrieval impairments
  • >21 years of age right handed
  • speaker of English as the preferred language
  • >6 grade education

Exclusion Criteria:

  • history of developmental learning difficulties
  • history of prior neurological illnesses
  • chronic medical illnesses that restrict participation in speech therapy
  • alcohol or drug dependence
  • severe uncorrected impairments of vision or hearing
Sexes Eligible for Study: All
21 Years to 90 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00764400
R15DC009690( U.S. NIH Grant/Contract )
3R15DC009690 ( U.S. NIH Grant/Contract )
R15DC009690 ( U.S. NIH Grant/Contract )
No
Not Provided
Not Provided
Dr. Anastasia Raymer, Old Dominion University
Old Dominion University
National Institute on Deafness and Other Communication Disorders (NIDCD)
Principal Investigator: Anastasia M Raymer, PhD Old Dominion University
Old Dominion University
May 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP