Cognitive Therapy to Improve Word Finding

Sponsor
Georgetown University (Other)
Overall Status
Completed
CT.gov ID
NCT00494520
Collaborator
(none)
78
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2
59
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Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Errorful training condition
  • Procedure: Errorless training condition
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
78 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Learning Paradigms in Aphasia Rehabilitation
Study Start Date :
Jul 1, 2004
Actual Primary Completion Date :
Jun 1, 2009
Actual Study Completion Date :
Jun 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Experimental: Errorful training condition

A type of anomia rehabilitation paradigm which allows for errors. The intervention involves providing minimal auditory cues to allow for errors in picture naming.

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.

Experimental: Errorless training condition

A type of anomia rehabilitation paradigm in which the situation surrounding the performance of the desired task (i.e., picture naming) is controlled to prevent errors. The intervention involves providing maximal auditory cues to prevent errors in picture naming.

Procedure: 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.

Outcome Measures

Primary Outcome Measures

  1. Improved picture naming of trained words. [Following conclusion of word treatment.]

    Overall accuracy of named trained items

Secondary Outcome Measures

  1. Improved picture naming of trained words. [At 6 months after conclusion of word treatment]

    Overall accuracy of named trained items

  2. Improved picture naming of untrained words. [Following conclusion of word treatment.]

    Overall accuracy of named untrained items

  3. Improved picture naming of untrained words. [At 6 months after conclusion of word treatment]

    Overall accuracy of named untrained items

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Georgetown University Medical Center Washington, D.C. District of Columbia United States 20057

Sponsors and Collaborators

  • Georgetown University

Investigators

  • Principal Investigator: Rhonda B. Friedman, Ph.D., Georgetown University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Georgetown University
ClinicalTrials.gov Identifier:
NCT00494520
Other Study ID Numbers:
  • R01DC006934-01
First Posted:
Jun 29, 2007
Last Update Posted:
Sep 19, 2017
Last Verified:
Apr 1, 2014
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Georgetown University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 19, 2017