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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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07143630
Enrollment
2
Registered
2025-08-27
Start date
2025-08-28
Completion date
2026-04-11
Last updated
2026-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

postural balance, balance impairment, rehabilitation, neuromuscular electrical stimulation, abdominal muscle

Brief 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.

Detailed description

Stroke is a leading cause of long-term disability and frequently results in impaired balance and trunk muscle weakness, limiting independence in daily life. Abdominal muscles are essential for postural stability, and their weakness may adversely affect mobility and functional outcomes in stroke patients. Neuromuscular electrical stimulation (NMES) is a safe rehabilitation method used to promote muscle contraction and improve strength. While NMES has shown positive effects on limb muscles, its impact on abdominal muscles and balance remains insufficiently studied. In this prospective randomized controlled trial, participants will be randomly allocated into two groups. The control group will perform core stabilization exercises, while the intervention group will receive core stabilization exercises combined with abdominal NMES. Balance will be assessed using validated clinical scales, and abdominal muscle thickness will be measured by ultrasound. The study aims to determine the additional effects of abdominal NMES on balance, trunk control, and functional recovery in stroke patients.

Interventions

DEVICENeuromuscular 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.

BEHAVIORALCore 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.

Sponsors

Başakşehir Çam & Sakura City Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

This study is a prospective, randomized, parallel-group trial. Stroke patients will be randomly assigned to one of two groups: (1) an intervention group receiving neuromuscular electrical stimulation (NMES) applied to the abdominal muscles in addition to core stabilization exercises, or (2) a control group performing only core stabilization exercises.

Eligibility

Sex/Gender
ALL
Age
18 Years to 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.

Design outcomes

Primary

MeasureTime frameDescription
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.

Secondary

MeasureTime frameDescription
Trunk Control (Trunk Control test)Baseline and after 15 sessions (≈3 weeks)]
Fear of Falling (Visual Analog Scale - VAS)Baseline and after 15 sessions (≈3 weeks)]Fear of falling will be evaluated using a Visual Analog Scale (VAS; score range: 0-10 cm, where 0 = no fear and 10 = maximum fear). Higher scores indicate greater fear of falling.
Change in Postural Control (Postural Assessment Scale for Stroke Patients)Baseline and after 15 sessions (≈3 weeks)]Postural control will be assessed using the Postural Assessment Scale for Stroke Patients (PASS; score range: 0-36). Higher scores indicate better postural control, lower scores indicate worse control.
Functional Ambulation (Functional Ambulation Classification - FAC)Baseline and after 15 sessions (≈3 weeks)]Ambulation will be measured using the Functional Ambulation Classification (FAC; score range: 0-5). Higher scores indicate better functional ambulation.
Mobility (Timed Up and Go Test - TUG)Baseline and after 15 sessions (≈3 weeks)]Mobility will be assessed using the Timed Up and Go Test (TUG; measured in seconds). Lower times indicate better mobility, higher times indicate worse mobility.
Motor Recovery (Brunnstrom Stages)Baseline and after 15 sessions (≈3 weeks)]Motor recovery will be assessed using Brunnstrom Stages of Motor Recovery (score range: Stage 1-6). Higher stages indicate better motor recovery.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORTuba SARIKAYA

Başakşehir Çam & Sakura City Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 16, 2026