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Clinical Trials/NCT02999360
NCT02999360
Completed
Not Applicable

Aerobic Exercise and Aphasia Treatment

NYU Langone Health1 site in 1 country8 target enrollmentDecember 19, 2016
ConditionsAphasia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aphasia
Sponsor
NYU Langone Health
Enrollment
8
Locations
1
Primary Endpoint
The Aphasia Communication Outcome Measure (ACOM) (Hula et al., 2015)
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of the study is to determine if speech therapy can be enhanced by Aerobic Exercise (AE). Investigators will use a single subject design to determine if aphasia therapy result in greater gains when combined with aerobic exercise.

Detailed Description

Aim 1: To test the feasibility of a research study that combines speech therapy with aerobic exercise (AE). Participants will be alternately assigned to receiving AE during during a 30 minute break from speech therapy. Aim 2: To test the preliminary efficacy of combining speech therapy with AE to promote language improvements in aphasia. These data will inform the design of a large, controlled clinical trial

Registry
clinicaltrials.gov
Start Date
December 19, 2016
End Date
September 20, 2019
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Aphasia severity based on Western Aphasia Battery-Revised (WAB-R) aphasia quotient(AQ)\>
  • An AQ of 51-75 correlates to moderate aphasia severity and an AQ of 76 and above correlates to mild aphasia severity. Only participants with mild to moderate aphasia (WAB AQ\>50) will be included. The Aphasia Quotient (AQ) is an essential summary value of the individual's aphasic deficit and is proportional to the severity of aphasia regardless of the type of aphasia or etiology of aphasia. Type of aphasia is not an inclusionary/exclusionary criterion because the focus is on language recovery regardless of aphasia type.
  • The inclusionary criterion regarding etiology is aphasia post ischemic stroke; no specific location of stroke is required.
  • Associated cognitive deficits are not a part of the inclusionary/exclusionary criteria because aphasia is a language disorder and the treatment is a language treatment.
  • English is primary language (patient report). Participant may have exposure to another language however English is the native language and primary language used for communication premorbidly.
  • At least 9 months post CVA (patient report and confirmed by medical records review when records available). The participant must be at least 9 months post stroke, which is considered to be the chronic stage therefore there is no restriction on the maximum number of months/years post stroke.
  • Able to participate in AE based on MD screening that follows recommendations for exercise in stroke patients .
  • Have a history of only one stroke.
  • Independent in walking (with or without assistive device).
  • Medically stable.

Exclusion Criteria

  • MD considers participant unable to comply with study requirements.
  • MD evaluates medication history and determines if current medications will have a negative impact and if so MD will not recommend patient inclusion.
  • Mood will first be screened by the Beck Depression Inventory screen and then assessed with the Beck Depression Inventory (BDI) if the participant does not pass the screening. This is a 21-item self-report assessment designed specifically to identify depression. The items are scored 0 (no problem) to
  • Thus, the possible score is between 0 -
  • A score of 9 or lower is the usual threshold to separate depressed from non-depressed subjects. If a subject scores 10 or higher the subject will not be included in the study and the MD will discuss with the subject the possibility of a referral for a psychiatric evaluation.
  • Stroke due to intracranial hemorrhage primarily due to bleeding from ruptured aneurysm or arteriovenous malformation.
  • Progressive stroke (primary progressive aphasia diagnosis)
  • Comorbid neurological diagnosis (e.g. MS, PD, dementia)
  • Unable to perform the required exercises due to a) medical, b) musculo-skeletal, or c) neurological problems (for details see below, a-c)
  • medical problems: unstable cardiovascular condition, or other serious cardiac conditions (for example, anyone meeting New York Heart Association Class IV criteria, hospitalization for myocardial infarction or heart surgery within 120 days, severe cardiomyopathy or documented serious and unstable cardiac arrhythmias)

Outcomes

Primary Outcomes

The Aphasia Communication Outcome Measure (ACOM) (Hula et al., 2015)

Time Frame: 24 Weeks

Patient-reported outcome measure of communicative functioning for persons with aphasia

The Boston Naming Test

Time Frame: 24 Weeks

The examiner begins with Item 1 and continues through Item 60, unless the patient is in distress or refuses to continue. The patient is told to tell the examiner the name of each picture and is given about 20 seconds to respond for each trial. The examiner writes down the patient's responses in detail, using codes. If the patient fails to give the correct response, the examiner at her or his discretion may give the patient a phonemic cue, which is the initial sound of the target word. After the patient completes the test, the examiner scores each item + or - according to the response coding and scoring procedures

Study Sites (1)

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