Transcranial Direct Current Stimulation for Post-stroke Fatigue

🩺 Protocol Summary

The investigators hypothesize that delivery of anodal tDCS to the left frontal head region will reduce fatigue severity following stroke.

Primary Research Facility: Weill Cornell Medicine, 525 E. 68th St, Baker Pavilion, F-2106 (New York, New York)

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

Diagnosed with, undergoing evaluation for, or seeking treatment related to Fatigue?

🔍 Study Population / Focus Area (Source: Protocol Primary Condition)

Aged 18 Years or older?

🔍 Protocol Specified Minimum Age: 18 Years

Able to attend required clinic visits at Weill Cornell Medicine, 525 E. 68th St, Baker Pavilion, F-2106 (New York, New York)?

🔍 Logistical Requirement: Site at Weill Cornell Medicine, 525 E. 68th St, Baker Pavilion, F-2106

📍 Primary Site Map

Site: Weill Cornell Medicine, 525 E. 68th St, Baker Pavilion, F-2106 — New York, New York

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.