Fact CheckerSign in

NCT06997744Not yet recruiting

TENS for Limb Function in Stroke: Design and Rationale for a Randomized Trial

Comparative Effects of 2Hz Versus 100Hz Transcutaneous Electrical Nerve Stimulation on Upper Limb Motor Function Post-Stroke: Design and Rationale for a Randomized Trial

Source: ClinicalTrials.gov · Last updated 28 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study tests whether slow or fast electrical nerve stimulation (TENS) works better to improve arm movement in people recovering from a stroke. Participants will receive TENS on their weak arm three times a week for eight weeks. The results will help find the best TENS setting to support stroke recovery.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
156 (estimated)
First submitted
21 May 2025
Start date
1 Oct 2025
Primary completion date
30 Sept 2027
Lead sponsor
CHENGNING Song
Diseases
Stroke
NCT number
NCT06997744

What you commit to

  • Study type: Interventional
  • Planned participants: 156
  • From 1 Oct 2025 to the primary completion date, 30 Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current participation in another clinical trial or drug study

Other illness

  • Uncontrolled medical, cardiovascular, or orthopedic conditions
  • Contraindications to TENS (e.g., implanted cardiac pacemaker, skin allergies)

Other

  • Receptive aphasia preventing informed consent or cooperation
  • Significant peripheral neuropathy affecting upper limbs
  • Severe contractures in the shoulder, elbow, wrist, or fingers

Who the study is looking for

  • Age 18 to 85 years
  • Clinical diagnosis of stroke (ischemic or hemorrhagic) within the past 10 days to 2 months
  • Presence of voluntary movement in the non-paretic arm and at least minimal antigravity movement in the paretic shoulder
  • At least 5 degrees of active wrist extension on the paretic side
  • Able to provide informed consent

Age in the registry: 40 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fuyong People's Hospital, Bao'an District, Shenzhen
Coordinator of this site? Confirm its status
ShenzhenChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.