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Combined Language and Arm Therapy for Chronic Stroke Survivors

Tests a combined language and robot-assisted arm program in adults with chronic stroke.

Plain-language title generated from the registry record
Registry title: Combined Aphasia and Robot-Assisted Arm Treatment for Chronic Stroke Survivors

Key facts

Where
Valhalla, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 90 years old?

Source: NCT07000019, who can take part

Where in United States

  • Westchester Medical Center / New York Medical CollegeValhalla, United StatesNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
New York Medical College
Trial code
NCT07000019
Record updated
31 May 2025
Original description
The goal of this clinical trial is to learn if a program that combines language and arm treatment can improve language and movement problems in people with chronic stroke. The mains questions it aims to answer are:Read full original descriptionShow less

Combined Aphasia and Robot-Assisted Arm Treatment for Chronic Stroke Survivors

The goal of this clinical trial is to learn if a program that combines language and arm treatment can improve language and movement problems in people with chronic stroke. The mains questions it aims to answer are:

* To determine the extent to which this combined treatment can improve language. * To determine the extent to which the combined treatment can improve arm movements.

Researchers will compare the effects of this combined treatment with treatment that targets arm movements alone.

Inclusion: Male or female patients between 18-90 years of age; Right-handed prior to stroke; English-speaking (monolingual); History of single left-hemisphere stroke at least 6 months prior to enrollment; Presence of aphasia and naming deficits on Western Aphasia Battery (WAB-R); Comprehension score above 4 on WAB-R; Unilateral upper limb paresis (Fugl-Meyer Upper Extremity score <56); Documentation of signed Informed Consent by the study participant.

Exclusion: Diagnosis or history of speech impairment prior to stroke; Inability to perform screening tasks due to severe language and/or cognitive impairment; Condition limiting passive movement in the range of motion required for robotic therapy (e.g. fixed contracture); Any medical or psychiatric condition that may impact participation or compliance with study procedures or activities in the opinion of the investigator; Severely limited speech output (score below 2 on spontaneous speech portion of WAB-R).

ClinicalTrials.gov NCT07000019