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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00764400
Other study ID # R15DC009690
Secondary ID 3R15DC009690
Status Completed
Phase N/A
First received September 30, 2008
Last updated April 4, 2018
Start date August 2008
Est. completion date July 2013

Study information

Verified date April 2018
Source Old Dominion University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date July 2013
Est. primary completion date June 2013
Accepts healthy volunteers No
Gender All
Age group 21 Years to 90 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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.

Locations

Country Name City State
United States Old Dominion University Speech and Hearing Clinic Norfolk Virginia

Sponsors (2)

Lead Sponsor Collaborator
Old Dominion University National Institute on Deafness and Other Communication Disorders (NIDCD)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Daily Probe Picture Naming daily probes from three times per week for up to 3 months and one month posttreatment
Secondary Western Aphasia Battery pre-treatment and at treatment completion
Secondary Boston Naming Test pretreatment and at treatment completion
Secondary Discourse Sample pre-treatment and at treatment completion
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