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Novel Assistive Device and Functional Electrical Stimulation Therapy

Early Rehabilitation of Post Stroke Lower Limb Weakness Using Novel Assistive Device and Functional Electrical Stimulation Therapy

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07090187
Enrollment
10
Registered
2025-07-29
Start date
2025-08-15
Completion date
2026-06-03
Last updated
2025-07-29

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

Conditions

Rehabilitation

Brief summary

Stroke causes neurological deficits, impacting walking, balance, strength, and independence, with high mortality and economic burden. Moreover, it brings serious mental and economic stress to patients and their families because of loss of independence. Current rehabilitation methods include standard therapy and electrical stimulation. This study introduces a novel hybrid approach combining use of an assistive device, the LegoPress, paired with closed-loop functional electrical stimulation for subacute stroke patients' lower limbs in a seated position, aiming to improve motor function particularly gait and balance.

Detailed description

The LegoPress is a passive assistive device that allows patients to undergo FES therapy while remaining in seated position. This is crucial for stroke patients as in the early acute phase they are at a higher risk of falling due to balance and mobility issues. The LegoPress is equipped with potentiometers and force sensors to measure the distance and force in flexion and extension. Therefore, when the LegoPress paired with FES, it can be performed in a closed loop where a maximum current is set for patient safety and can provide flexion/extension. Then based off this current the stimulation current can be modulated according to the position desired by the clinician. It can also be an alternative to cycling FES by featuring different movement functions such as simultaneous leg press action (in tandem), gait-simulation action (closest to walking), or sequential (one leg after the other). The efficacy of the LegoPress FES protocol has yet to be tested in the clinic and with stroke patients, this study therefore is motivated by investigating the feasibility of this proposed novel method as well as its clinical outcomes.

Interventions

DEVICELegoPress , Novel assistive device

novel assistive device for rehabilitation using functional electrical stimulation

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* \*Inclusion Criteria:\* * Ages 18 to 70 (max of 70 years to avoid fatigue or exhaustion in elderly patients) * Patients with acute ischemic or hemorrhagic stroke, verified by CT or MRI * Patients with power in the paretic lower limb synergistic extension = 2 or more on the MRC scale * \*

Exclusion criteria

\* * Patients presenting with paraplegia, ataxia, or severe sensory impairment * Patients with subarachnoid hemorrhage * Subjects with implanted electronic devices, such as cardiac pacemakers or any metallic implants in the lower limbs * Patients with other severe medical comorbidities, including: * Severe osteoarthritis * Liver dysfunction * Kidney dysfunction * Cardiovascular dysfunction * Patients with severe cognitive impairment preventing task completion, verified by a score of less than 7 on the Abbreviated Mental Test (AMT) * Patients who are: * Uncooperative * Hemodynamically unstable * Have a disturbance of consciousness * Patients with burns or any skin lesions at the sites of stimulation

Design outcomes

Primary

MeasureTime frameDescription
Efficacy and tolerability of LegoPress device in conjunction with functional electrical stimulation (FES) on the paretic lower limb in acute stroke patients.For each participant in intervention group: 15 sessions of Lego Press + closed loop FES. Combined with 15 sessions of regular physiotherapy5 sessions per week, 1 per day, 3 weeks total.Objective: To quantify motor function improvements and Gait performance in patients undergoing combined Lego Press + Closed-Loop FES therapy with standard physiotherapy. Primary Outcomes 1. Motor Function Assessment Tool: Medical Research Council (MRC) scale for motor power. 2. Gait Speed 10-Meter Walk Test (10MWT) Timed Up and Go Test (TUG) Assessment Schedule: t=0: Baseline (before first session) t=1: Midpoint (after 7 sessions) t=2: Post-intervention (after 15 sessions, 3 weeks total)

Secondary

MeasureTime frameDescription
Over all functional improvement and Functional IndependenceEach participant will undergo: 15 sessions of Lego Press + closed-loop Functional Electrical Stimulation (FES) 15 sessions of conventional physiotherapy 5 sessions/week, 1 session/day over 3 weeks1. Overall Motor Function Assessment Tool: Fugl-Meyer Assessment for Lower Extremity (FMA-LE) Timepoints: t=0, t=1, t=2 2. Daily Living Functionality Functional Ambulation Category (FAC). Assessment Schedule: t=0: Baseline (before first session) t=1: Midpoint (after 7 sessions) t=2: Post-intervention (after 15 sessions, 3 weeks total)

Countries

Egypt

Contacts

Primary ContactSara M. Sara Mohammad Gaber Mahmoud, MD
Drsaramohammad33@gmail.com+20 01122240327
Backup ContactNeivine M. Nevine El -Nahas, Professor
nevine_elnahas@med.asu.edu.eg+20 12 27910517

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026