Assessment of a Physio-neuro Platform (SynPhNe) for Home-based Retraining of Hand Function in Stroke Survivors

🩺 Protocol Summary

The goal of this study is to: 1. Assess the usability of the SynPhNe device in a home environment. 2. Evaluate the efficacy of the SynPhNe home use device to improve motor hand function in chronic stroke subjects as compared to standard care alone.

Primary Research Facility: Spaulding Rehabilitation Hospital (Boston, Massachusetts)

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 Stroke?

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

Aged between 21 Years and 80 Years?

🔍 Protocol Specified Age Range: 21 Years to 80 Years

Able to attend required clinic visits at Spaulding Rehabilitation Hospital (Boston, Massachusetts)?

🔍 Logistical Requirement: Site at Spaulding Rehabilitation Hospital

📍 Primary Site Map

Site: Spaulding Rehabilitation Hospital — Boston, Massachusetts

💰 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.