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Active, not recruitingNCT07629882Updated Jun 5, 2026

Functional Electrical Stimulation Versus Whole-Body Vibration in Post-Stroke Rehabilitation

An interventional study of Functional Electrical Stimulation and Whole Body Vibration Training in Stroke (CVA) or TIA, sponsored by Riphah International University. Active, not recruiting at 1 site in Pakistan. Open to participants aged 35 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-06-05.

Sponsored by Riphah International University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as active, not recruiting.
  • Registered 11 months after the study started (first participant enrolled Jun 2025, registered Jun 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
35 Years to 70 Years
Sex
All
01

Study summary

This study will compare the effects of Functional Electrical Stimulation (FES) and Whole Body Vibration Training (WBVT) on lower limb motor control, balance, and physical performance in post-stroke patients. It will be a single-blinded randomized clinical trial including 34 participants, who will be allocated into two groups. Both groups will receive their respective interventions 4 days per week for 8 weeks. Outcomes will be assessed at baseline and after 8 weeks using the Fugl-Meyer Assessment for lower extremity motor control, Berg Balance Scale for balance, and Barthel Index for physical performance.

Read the detailed description

Stroke is an acute focal injury of the central nervous system caused by a vascular source, which results in neurological deficits and can cause disability or death. Stroke can lead to motor weakness, sensory deficiency and loss of motor control. Patients who have had a stroke frequently experience issues with their balance, gait and physical performance. Whole-Body Vibration Training (WBVT) is a non-pharmacological intervention that transmits vibration stimulation throughout the body and has demonstrated promise in improving balance, mobility, and physical function in stroke rehabilitation. Functional Electrical Stimulation (FES) is a rehabilitation technique that helps stroke survivors regain motor skills by stimulating certain nerves with electrical impulses applied via the skin's surface, which causes paretic muscles to move. FES can be utilized to improve physical performance, muscle strength, and balance in stroke patients. Strokes frequently lead to poor physical performance, diminished balance, and impaired lower limb motor control, all of which have an adverse effect on daily functioning and quality of life. This study aims to compare the effects of Functional Electrical Stimulation and Whole Body Vibration Training on lower limb motor control, balance, and physical performance in post-stroke patients.

02

Conditions studied

  • Stroke (CVA) or TIA

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Keywords

  • Functional Electrical Stimulation (FES)
  • Stroke Rehabilitation
  • Physical Performance
  • Balance
  • Lower Limb Motor Control
  • Whole Body Vibration Training (WBVT)
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's planned enrollment of 34 is below the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,133 studies on the registry; 633 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • the patient is between the ages of 35 and 70.
  • Both male and female participants will be included.
  • Chronic post-stroke patients from 6 months to 1 year.
  • Stroke patients who have a neurological impairment.
  • Individuals who experienced a single stroke in either the left or right hemisphere of the brain.
  • Lower limb motor impairment with Fugl-Meyer Lower Extremity Score ≤ 28.
  • Barthel Index Score ≥ 60.
  • Berg Balance Scale Score ≥ 21.

Exclusion criteria

Exclusion Criteria:

patients suffering from unstable cardiac condition, severe hypertension, congestive heart failure, aphasia, or cognitive impairments for which exercises are contraindicated.

  • Patients with recurrent stroke.
  • Patients undergoing other form of lower limb stimulation therapy concurrently.
  • Severe orthopedic conditions or joint deformities affecting lower limb.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
34 participants (estimated)

Study arms

  • Experimental
    Functional Electrical Stimulation Group

    Participants in this arm will receive transcutaneous Functional Electrical Stimulation for lower limb rehabilitation for 8 weeks. Stimulation will be applied to selected lower limb muscles including tibialis anterior, quadriceps, hamstrings, and peroneal muscles. Treatment parameters will progress according to tolerance, including intensity, session duration, and functional movement integration. Outcomes will be assessed at baseline and after 8 weeks.

    Device: Functional Electrical Stimulation

  • Active comparator
    Whole Body Vibration Training Group

    Participants in this arm will receive Whole Body Vibration Training using a vibration platform for 8 weeks. Training will include progressive activities such as standing, semi-squat, heel raises, dynamic squatting, side-to-side weight shifting, and one-leg stance. Vibration frequency, duration, and exercise difficulty will be gradually progressed according to tolerance. Outcomes will be assessed at baseline and after 8 weeks. After this, go to Interventions and add Functional Electrical Stimulation and Whole Body Vibration Training, then assign each intervention to its matching arm.

    Device: Whole Body Vibration Training

Interventions

  • DeviceFunctional Electrical Stimulation

    Functional Electrical Stimulation will be delivered transcutaneously to selected lower limb muscles for 8 weeks. Stimulation will target tibialis anterior, quadriceps, hamstrings, peroneal muscles, and other lower limb muscles according to patient need and tolerance. The intervention will use biphasic symmetrical pulsed current with progressive intensity, duration, and functional movement integration. Treatment will be supervised by a physiotherapist, and outcomes will be assessed at baseline and after 8 weeks.

    Also known as: FES, Neuromuscular Electrical Stimulation, Electrical Stimulation Therapy

  • DeviceWhole Body Vibration Training

    Whole Body Vibration Training will be delivered using a vibration platform for 8 weeks. Participants will perform progressive lower limb activities including standing, semi-squat, heel raises, dynamic squatting, side-to-side weight shifting, and one-leg stance exercises. Frequency, duration, and difficulty will be progressed according to patient tolerance under physiotherapist supervision.

    Also known as: Whole Body Vibration, WBV Training

06

What researchers measure

Primary outcomes

  1. lower Limb Motor Control

    Assessed using the Fugl-Meyer Assessment for Lower Extremity.

    Time frame: Baseline and 8 weeks post-intervention

Secondary outcomes

  1. Balance

    Assessed using the Berg Balance Scale.

    Time frame: Baseline and 8 weeks post-intervention

  2. Physical Performance

    Assessed using the Barthel Index Scale.

    Time frame: Baseline and 8 weeks post-intervention

07

Study locations

1 site
  • Hafiz Physiotherapy Center
    Gujrat, Punjab Province 50700, Pakistan
08

References and documents

Individual participant data

Plan to share: No — The individual participant data sharing plan has not yet been finalized.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07629882
Lead sponsor
Riphah International University
Responsible party
Sponsor
First posted
Jun 5, 2026
Start date
Jun 5, 2025
Primary completion
Jul 6, 2026 (estimated)
Completion
Aug 6, 2026 (estimated)
Last update
Jun 5, 2026

Study contacts

Ambreen Iqbal IQBAL
study chair · Riphah International University Role

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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