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Not yet recruiting Not applicable NCT06950060

AMPLIFI: Adaptive Modulation of Plasticity Through Lactate and Fitness Interventions

No applicable phase (e.g. observational)
Conditions: Stroke, Chronic Aging Cognitive Decline Motor Dysfunction Neuroplasticity

Sponsor: University of Alabama at Birmingham

trial.available_in: БГ
Overview
The AMPLIFI study (Adaptive Modulation of Plasticity through Lactate and Fitness Interventions) investigates how short-term aerobic exercise influences brain plasticity and learning in older adults and stroke survivors. The study compares three groups: one performing aerobic cycling at an intensity that elevates lactate levels, one performing low-intensity exercise, and one receiving health education without exercise. All participants will complete motor learning tasks and undergo brain-stimulation testing using transcranial magnetic stimulation (TMS) to assess how well the brain responds to training. The goal is to understand whether different types of exercise can improve brain function, movement, and memory, and how the body's response to exercise (like lactate levels) might support brain health. This research may help identify low-cost, non-invasive interventions-such as targeted exercise-that improve motor and cognitive outcomes in aging and stroke recovery.
Description
The AMPLIFI study is a mechanistic clinical trial designed to investigate the neurophysiological effects of acute aerobic exercise on cortical plasticity and motor learning in older adults and individuals with chronic stroke. Participants are randomized into one of three groups: (1) moderate-to-high intensity aerobic exercise at lactate threshold, (2) moderate intensity aerobic exercise, (3) low-intensity aerobic exercise, or (4) education-only control. The primary outcome measure is cortical inhibition, assessed using transcranial magnetic stimulation (TMS) measures including short-interval intracortical inhibition (SICI), long-interval intracortical inhibition (LICI), and intracortical facilitation (ICF). Secondary outcomes include performance on upper extremity motor tasks, measures of verbal and executive function, and blood lactate levels. Participants complete three sessions over 2-3 weeks, including baseline assessments, VO2 max testing, multiple blood draws, and cognitive and motor testing. The exercise intervention is delivered via stationary cycling at intensities tailored using individual VO2 max data and lactate monitoring. Genetic and biochemical assays will be performed on blood samples to explore associations between metabolic and neural response. This study will clarify how lactate-related exercise intensity impacts cortical inhibition and whether those effects support improvements in motor learning. Findings may help define the mechanisms by which exercise promotes neuroplasticity and support individualized rehabilitation strategies for aging and post-stroke populations.
Who can participate
Inclusion Criteria: For All Participants: * Able to provide informed consent * Right-handed (for TMS consistency) * English-speaking * Clearance for moderate-intensity aerobic exercise * Able to safely sit and pedal a stationary cycle ergometer * No contraindications to TMS (e.g., no metal in skull, pacemakers, or seizure history) Younger Adults (18-35): * No history of neurological or psychiatric conditions * Not currently on medications that affect the central nervous system Older Adults (60-85): * No diagnosis of dementia * Independent in activities of daily living * No stroke history Stroke Survivors (40-85): * At least 6 months post-stroke (chronic phase) * Medically stable and cleared for aerobic exercise * Able to engage in motor learning task (with or without hemiparetic adaptations) Exclusion Criteria: * History of epilepsy or seizures * Current substance abuse or uncontrolled psychiatric disorder * Severe cardiovascular disease or unstable medical condition * Pregnancy * Contraindications to TMS or exercise testing (e.g., implanted neurostimulators, severe hypertension) * Participation in another interventional trial within the past 30 days
Interventions
High intensity cycling
BEHAVIORAL
Low-intensity cycling
BEHAVIORAL
Health education session
BEHAVIORAL
Moderate Intensity Aerobic Exercise
BEHAVIORAL
Locations 1
United States (1)
CH19 933 19th St S
Birmingham , Alabama
Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
85 Years
Healthy volunteers
No
Start date
14.05.2026
Completion date
01.01.2030
Registry ID
NCT06950060
Source
clinicaltrials.gov
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