Rehabilitation and Prophylaxis of Anomia in Primary Progressive Aphasia

Sponsor
Georgetown University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02675270
Collaborator
National Institute on Deafness and Other Communication Disorders (NIDCD) (NIH), National Institute on Aging (NIA) (NIH), Johns Hopkins University (Other)
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Study Details

Study Description

Brief Summary

The goal of this study is to remediate word-finding problems in patients who have Primary Progressive Aphasia (PPA) or Alzheimer's Disease and to delay the further progression of word-finding impairment. The current approach is novel in that it contains a prophylaxis component in which the investigators attempt to strengthen neural connections that remain functional, making them more resistant to degradation as the disease progresses. While the study is specific in its targeting of word-finding problems, a successful outcome would bode well for other studies aimed at prevention or reversal of declining cognitive functions in dementia. One set of participants with PPA will receive practice with picture naming in two conditions: viewing the picture and repeating the name; and viewing the picture with its written name, plus reading and writing the name. Another set of participants with PPA or Alzheimer's Disease will be trained in two different conditions: learning about the word's semantic features (meaning); and learning about the word's lexical features (letters and sounds). Naming of pictures trained in each of these conditions will be compared, at three time intervals post-training, with naming of pictures tested before the study but never trained. It is predicted that the pairing of the picture with its written name, combined with the motor task of writing the name, will result in a greater ability to name the picture at a later date than simple practice viewing the picture and repeating the name. Furthermore, it is predicted that participants who have difficulty understanding concepts will be more likely to respond to semantic treatment, while participants who have difficulty connecting words with concepts will be more likely to respond to lexical treatment.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Phonological
  • Behavioral: Orthographic
  • Behavioral: Semantic
  • Behavioral: Lexical
  • Behavioral: Untrained
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
84 participants
Allocation:
Non-Randomized
Intervention Model:
Sequential Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Actual Study Start Date :
Nov 1, 2011
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Phonological, Orthographic, Untrained

Behavioral: Phonological
This treatment involves picture viewing and word repetition.

Behavioral: Orthographic
This treatment involves picture viewing, reading, and writing.

Behavioral: Untrained
These words are not trained during the treatment phase.

Experimental: Semantic, Lexical, Untrained

Behavioral: Semantic
This treatment involves learning about the semantic features (meaning) of each trained word.

Behavioral: Lexical
This treatment involves learning about the lexical features (letters and sounds) of each trained word.

Behavioral: Untrained
These words are not trained during the treatment phase.

Outcome Measures

Primary Outcome Measures

  1. Change in picture naming accuracy for words within each treatment condition during treatment [baseline, 7 months]

    The change in picture naming accuracy for trained words will be compared with the change in picture naming accuracy for words that were tested at baseline but never trained during the treatment phase.

Secondary Outcome Measures

  1. Change in picture naming accuracy for words within each treatment condition between baseline and first follow-up assessment [baseline, 14 months]

    The change in picture naming accuracy for trained words will be compared with the change in picture naming accuracy for words that were tested at baseline but never trained during the treatment phase.

  2. Change in picture naming accuracy for words within each treatment condition between baseline and second follow-up assessment [baseline, 21 months]

    The change in picture naming accuracy for trained words will be compared with the change in picture naming accuracy for words that were tested at baseline but never trained during the treatment phase.

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of Primary Progressive Aphasia (PPA; including Frontotemporal Dementia, Semantic Dementia, or a similar condition) or Diagnosis of Alzheimer's Disease

  • At least 10 years of education

  • Ability to follow spoken instructions

  • Medically stable

  • First language is English, or fluent in English since childhood

  • Willing to participate over a period of two years

Exclusion Criteria:
  • No history of additional neurological problems

  • No history of substance abuse or psychiatric problems

Contacts and Locations

Locations

Site City State Country Postal Code
1 Georgetown University Medical Center Washington District of Columbia United States 20057
2 Johns Hopkins University Baltimore Maryland United States 21287

Sponsors and Collaborators

  • Georgetown University
  • National Institute on Deafness and Other Communication Disorders (NIDCD)
  • National Institute on Aging (NIA)
  • Johns Hopkins University

Investigators

  • Principal Investigator: Aaron Meyer, PhD, Georgetown University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Aaron Meyer, PhD, Assistant Professor, Georgetown University
ClinicalTrials.gov Identifier:
NCT02675270
Other Study ID Numbers:
  • R01DC011317
First Posted:
Feb 5, 2016
Last Update Posted:
Aug 3, 2022
Last Verified:
Aug 1, 2022

Study Results

No Results Posted as of Aug 3, 2022