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NCT07143630Active, not recruiting

Abdominal Electrical Stimulation for Balance and Muscle Thickness in Stroke Patients

Effects of Abdominal Electrical Stimulation on Balance and Ultrasound-Measured Muscle Thickness in Stroke Patients: A Prospective Randomized Controlled Trials

Source: ClinicalTrials.gov · Last updated 15 Apr 2026

Brief summary (registry, in English)

Stroke is a leading cause of balance impairment and trunk muscle weakness, which restricts independence in daily activities. Neuromuscular electrical stimulation (NMES) is a safe rehabilitation method to activate muscles. This study will evaluate the effects of NMES applied to the abdominal muscles on balance and ultrasound-measured muscle thickness in stroke patients. The findings may provide evidence for new treatment strategies to enhance trunk function and improve quality of life after stroke.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
2 (estimated)
First submitted
20 Aug 2025
Start date
28 Aug 2025
Primary completion date
11 Apr 2026
Lead sponsor
Başakşehir Çam & Sakura City Hospital
Diseases
Stroke
NCT number
NCT07143630

What you commit to

  • Study type: Interventional
  • Planned participants: 2
  • From 28 Aug 2025 to the primary completion date, 11 Apr 2026
  • 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

  • Presence of balance problems prior to stroke.

Other illness

  • History of hemiplegia on the contralateral side of the body.
  • Medically unstable condition.
  • History of orthopedic or neurological disease that may cause balance impairment.
  • Presence of a cardiac pacemaker.
  • Diagnosis of malignancy.
  • Epilepsy.
  • Open wound or infection in the area where stimulation will be applied.

Other

  • Body mass index (BMI) ≥ 35
  • Pregnancy.
  • Lack of cooperation or inability to follow instructions.

Who the study is looking for

  • Age between 18 and 65 years.
  • At least 1 month since the onset of stroke.
  • Ability to maintain sitting balance without support.
  • Ability to stand with or without support.
  • Voluntary agreement to participate in the study (signed informed consent).

Age in the registry: 18 years to 65 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
Başakşehir Çam and Sakura City Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

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