Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Combined electrical stimulation and brain stimulation to help with foot drop after stroke

Official title: Combined Functional Electrical and Transcranial Direct Current Stimulation for Foot Drop: A Case Series

Run by Saint Joseph's University, Philadelphia · NCT07592221 · Data updated 2026-11-12

This study tests whether using both transcranial direct current stimulation (tDCS) and functional electrical stimulation (FES) together helps people who have trouble lifting their toes after a stroke.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorSaint Joseph's University, Philadelphia
Academic / other
Locations1 site (Philadelphia, Pennsylvania)
StatusRecruiting
StartedNovember 1, 2026
Main results expectedDecember 31, 2028
Study endsAugust 30, 2029
Registry record updatedOctober 22, 2026
Trial IDNCT07592221 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older who are at least six months post-stroke, can walk for 15 minutes (with or without an assistive device) and have foot drop without current rehabilitative care.

Probably not a fit

Individuals who cannot understand/tolerate the stimulation protocol or who have conditions like peripheral neuropathy or a history of seizures may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will examine if pairing tDCS with FES during physical therapy improves toe clearance and ankle movement in stroke survivors with foot drop. Participants will receive noninvasive brain stimulation on the scalp and electrical stimulation on the leg, along with leg-strengthening exercises. The goal is to see if the combination provides added benefit over standard therapy in reducing foot drop. The study is conducted at Saint Joseph's University in Philadelphia and is open to adults who are at least six months post-stroke and can walk for 15 minutes unaided or with a cane. Safety monitoring and specific eligibility criteria are applied to ensure appropriate inclusion and exclusion.

Why it matters

Potential benefit: If successful, participants may experience better toe clearance and improved walking ability due to more effective foot dorsiflexion.

How similar studies have gone: Previous work in related approaches has shown promise for combining neuromodulation with electrical stimulation to aid motor recovery, but this specific combination for foot drop post-stroke is exploratory.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria: To participate, you must be:

* 18 years or older
* Have had 1 or more strokes (\> 6 months) affecting ankle dorsiflexion.
* Discharged from all rehabilitative services.
* Can walk independently with/without using an assistive device such as a cane without an ankle-foot orthosis (AFO) for 15 minutes.

Exclusion Criteria: You must not have:

* An inability to repeat and understand 2-step commands.
* Peripheral neuropathy
* Damage to the skull or scalp, such as a fracture History of seizures or epilepsy Extremely high or low blood pressure or heart rate Chest pain or shortness of breath when you are resting Botox injections to your leg or foot in the last 4 months

Where it's running

  • Saint Joseph's University
    Philadelphia, Pennsylvania, United States
    Recruiting

Study contacts

  • Principal investigator: Gregory Thielman, EdD — Saint Joseph's University
  • Study coordinator: Greg Thielman, EdD
  • Email: gthielman@sju.edu
  • Phone: 8562667863

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.