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Active, not recruiting Not applicable

Abdominal Electrical Stimulation for Balance and Muscle Thickness in Stroke Patients

NCT07143630 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-08-28
Last updated
2026-04-15

Condition(s) studied

Stroke

Investigational drug(s) / intervention(s)

Neuromuscular Electrical StimulationCore Stabilization Exercises

Neuromuscular Electrical Stimulation: NMES will be applied to the abdominal muscles using a multichannel stimulator. Each session will last approximately 20 minutes, administered 5 times per week for a total of 15 sessions, in addition to core stabilization exercise program performed with the same frequency.

Core Stabilization Exercises: Participants will perform a structured core stabilization exercise program. The program will be administered 5 times per week for a total of 15 sessions.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * 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). Exclusion Criteria: * 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 balance problems prior to stroke. * Body mass index (BMI) ≥ 35 * Presence of a cardiac pacemaker. * Diagnosis of malignancy. * Epilepsy. * Pregnancy. * Open wound or infection in the area where stimulation will be applied. * Lack of cooperation or inability to follow instructions.

Primary outcome measure(s)

  • Change in Balance Performance (Berg Balance Scale) — Baseline and after 15 sessions (≈3 weeks)
    Balance will be assessed using the Berg Balance Scale (BBS; maximum score: 56, minimum score: 0). Higher scores indicate better balance, lower scores indicate worse balance.
  • Abdominal Muscle Thickness (Ultrasound) — Baseline and after 15 sessions (≈3 weeks)]
    Abdominal muscle thickness will be measured in millimeters by ultrasound at rest. Higher values indicate greater muscle thickness.

Trial sites (1)

FacilityCityRegionStatus
Başakşehir Çam and Sakura City Hospital Istanbul Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07143630 on ClinicalTrials.gov ↗ ← All trials in Turkey