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Aphasia Physical EXercise Study: Randomized Trial

Recruiting

High-intensity Exercise in Stroke Recovery: Randomized Trial

Who can join

Ages 18 to 80 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Aphasia following ischemic or hemorrhagic stroke
* Aphasia as determined by a standardized language test (Western Aphasia Battery Aphasia Quotient \< 93.8 at study intake)
* At least 6 months from the last stroke
* Proficient in English before the stroke
* At least 8 years of education
* Between the ages of 18 and 80
* Independent with ambulation without a device (single-point cane accepted)
* Medically stable with no contraindications to participate in regular physical exercise as determined by the patients' own primary care provider or other treating provider.

Exclusion Criteria:

* Prior history of dementia, neurologic illness (other than stroke), or recent (last 3 years) substance abuse
* Significant visual or hearing disabilities (e.g., neglect, uncorrected visual or hearing loss) that interfere with testing
* Self-report uncontrolled cardiorespiratory and/or metabolic disorders incompatible with exercise

About the study

The goal of this clinical trial is to evaluate the effects of a high-intensity exercise program on recovery in individuals with post-stroke aphasia. The high-intensity exercise program has been specifically designed for individuals with post-stroke aphasia and includes an interval training full-body workout, which can increase cardiovascular fitness, improve muscle strength and motor performance, and maximize cognitive and language gains. The main question this study aims to answer is:

• Does participation in a high-intensity exercise program lead to changes in physical health, language, cognitive, motor recovery, psychological and/or psychosocial domains?

Participants will be randomly assigned to either a high-intensity exercise program (target intervention) or a low-intensity exercise program (control intervention) delivered over 12-weeks in a group setting.

Outcome measures will be collected once immediately after the intervention period and once during the following 12-week maintenance period to capture short- and long-term effects of the exercise program.

What is being tested

Sponsor: University of California, Berkeley · Participants: 120 · Started: Dec 1, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07281313

Locations in the U.S.

CaliforniaUniversity of California, Berkeley, Berkeley
California State University, East Bay, Hayward
University of California, San Francisco, San Francisco
University of San Francisco, San Francisco

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.