Skip to main content
OpenTrials
Completed

NCT Number: NCT02675270

Rehabilitation and Prophylaxis of Anomia in Primary Progressive Aphasia

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Georgetown University Medical Center, Washington D.C., District of Columbia, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Phonological

Behavioral

This treatment involves picture viewing and word repetition.

Orthographic

Behavioral

This treatment involves picture viewing, reading, and writing.

Semantic

Behavioral

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

Lexical

Behavioral

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

Untrained

Behavioral

These words are not trained during the treatment phase.

Primary outcomes

  1. Change in picture naming accuracy for words within each treatment condition during treatment

    Time frame: 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 outcomes

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

    Time frame: 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

    Time frame: 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.

Sponsors and collaborators

Lead sponsor

Georgetown University

Other

Collaborators

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

Registry information

Important dates

Study start
2011
Primary completion
2023
Study completion
2024
First posted
Feb 5, 2016
Registry last updated
Sep 25, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.