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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00494520
Other study ID # R01DC006934-01
Secondary ID
Status Completed
Phase N/A
First received June 28, 2007
Last updated September 15, 2017
Start date July 2004
Est. completion date June 2009

Study information

Verified date April 2014
Source Georgetown University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Adults who sustain brain damage due to stroke, traumatic injury or surgery may develop difficulty finding words. This study compares the effectiveness of two behavior-based programs to improve picture naming ability in these individuals.


Description:

Difficulty finding words is common in patients with aphasia subsequent to left hemisphere stroke. This study will compare two cognitive therapies for the treatment of acquired word finding difficulties. The therapies use different types of cues. All participants will receive both therapies. Participants in this study will undergo a comprehensive and detailed assessment of language and other cognitive skills. The two treatments will be compared for their efficacy.


Recruitment information / eligibility

Status Completed
Enrollment 78
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Word finding difficulty subsequent to stroke, traumatic brain injury, brain surgery or other brain damage occuring at least 6 month prior to participation

- Ability to attend 2 sessions per week for several months at Georgetown University in Washington, DC

Exclusion Criteria:

- History of learning disabilities

- Best corrected vision less than 20/40

- Corrected hearing within functional limits

- Less than 10 years formal education

- Significant memory or comprehension problems

Study Design


Intervention

Procedure:
Errorful training condition
Errorful training condition: Participant saw a picture and named it without any cues. If an error was produced, the cue with the least amount of information was provided (e.g. for "pumpkin", "pu"). Cues with increasing information were provided until the picture was correctly named (e.g. for "pumpkin": "pump", "pumpki", then "pumpkin"). Once the correct name was provided, the trial ended.
Errorless training condition
Errorless learning (EL) condition: Participant saw a picture with its name, and repeated the word. The participant continued to name the picture as the auditory cues provided less and less of the word (e.g. for "banana" she would hear "banan", "bana" then "ba" and finally no cue). If an error was produced at any stage, the whole word was presented, the participant repeated it, and the trial ended.

Locations

Country Name City State
United States Georgetown University Medical Center Washington, D.C. District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Georgetown University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improved picture naming of trained words. Overall accuracy of named trained items Following conclusion of word treatment.
Secondary Improved picture naming of trained words. Overall accuracy of named trained items At 6 months after conclusion of word treatment
Secondary Improved picture naming of untrained words. Overall accuracy of named untrained items Following conclusion of word treatment.
Secondary Improved picture naming of untrained words. Overall accuracy of named untrained items At 6 months after conclusion of word treatment
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