Comparative Effects of SBES Versus TOT on Lower Limb Motor Function in Post-Stroke Patients
Comparative Effects of Synergy-Based Electrical Stimulation Versus Task-Oriented Training on Lower Limb Motor Function in Post-Stroke Patients
Stroke-induced lower limb impairments severely inhibit functional independence and mobility in survivors. Inventive techniques like Synergy-Based Electrical Stimulation (SBES) and Task-Oriented Training (TOT) support favorable rehabilitation results based on Neuroplasticity. This study aims to compare the effectiveness of these in restoring purposeful movements and enhancing motor functions in post-stroke patients.This study aims to compare the efficacy of (SBES) and Task-Oriented Training (TOT) in improving lower limb motor control in sub-acute post-stroke patients.
This study will be a single-blinded randomized clinical trial design. Participants, aged 40-60 will be recruited in this study by Non-Probability convenience sampling from Rehabilitation centers and Neurology departments. Informed consent and consistent attendance throughout the intervention will be required. Through the computerized table generator method of randomization, participants will be evenly divided into two groups. Both groups will receive conventional therapy, like stretching, strengthening, and isometrics, with modalities. Group A will receive 30 Hz electrical stimulation on the affected lower limb muscles (hip flexors, knee flexors, and ankle dorsiflexors) in a synergic pattern, for 60 minutes, thrice weekly for 6 weeks. Group B will engage in functional tasks for 60 minutes, thrice weekly for 6 weeks, repeated 10 times per set with 2 sets of each activity, plus an additional self-practice session. Outcome measures will be assessed at baseline and post-intervention stages by the Fugl-Meyer Assessment for motor recovery, Time UP and Go Test (TUG) and 10 Meter Walk Test for functional mobility, gait, and balance. The paired sample t-test will be used for within-group analysis in the parametric data and the Wilcoxon test for non-parametric data, whereas, for between-group analysis independent t-test will be used for parametric data and Mann Whitney U test will be used for non-parametric data. Statistical analysis will be done by using SPSS version 26.
Keywords: Lower Limb, motor control, SBES, Strength, Stroke, TOT.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
The synopsis will be presented to the Research Ethical Committee of Riphah International University, Lahore, for ethical approval to conduct this study.
RECRUITMENT:
Eligible participants will be recruited from Neurology departments and Rehabilitation centers.
RANDOMIZATION:
Patients will be recruited using a non-probability convenience sampling technique, and then they will be divided into two groups by simple random sampling through sealed, opaque envelopes.
BLINDNESS:
This study will be a single-blinded study in which the outcome assessor will be blind.
INTERVENTION:
Participants who will meet the inclusion criteria will be recruited, and written informed consent will be obtained before enrollment. The initial assessment will include the Fugl-Meyer Assessment to measure motor recovery and the 10-M Walk Test and TUG to evaluate functional mobility. Participants will be allocated to either the Synergy-Based Electrical Stimulation (SBES) group or the Task-Oriented Training group.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
-
-
Punjab Province
-
Lahore, Punjab Province, Paquistão, 54000
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Age: 40 to 60 years
- Both Male and Female participants
- In the sub-acute phase of stroke (1-6 months post-stroke) with lower limb motor impairment but with the ability to initiate at least trace muscle contraction (Grade ≥ 1).
- Participants must have the ability to understand and follow simple verbal commands with the Mini-Mental State Examination (MMSE) ≥ 26.
- Participants must have a first-ever ischemic and hemorrhagic stroke in the sub-acute stage.
- Participants who are functionally ambulatory and able to walk a minimum of 10 feet, with or without the use of assistive devices with a Functional Ambulation Category (FAC) score ≥ 2.
Exclusion Criteria:
- Participants have severe cognitive impairment and an inability to understand or follow instructions, and severe sensory impairment with profound sensory loss in the lower limb affecting balance or feedback-based training.
- Participants having orthopedic limitations like recent fractures, joint deformities, or surgeries affecting the lower limbs.
- Participants having implanted electrical devices like pacemakers are contraindicated for electrical stimulation
- Participants having a history of more than one stroke episode and or multiple infarcts.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Therapy
Hot pack and isometric exercises
|
Synergy based visible but comfortable muscle contraction in semi-supine position, surface electrodes on hip and knee flexors and dorsiflexors.• Intensity adjusted based on tolerance • Monitor muscle response and patient comfort Tot Sit-to-stand, reaching, weight shifting, gait training, ball-kicking, tandem/side walking• Increase intensity by slightly reducing assistance • Add unstable surfaces for gait |
|
Comparador Ativo: Conventional Therapy
Hot pack and isometric exercises
|
Synergy based visible but comfortable muscle contraction in semi-supine position, surface electrodes on hip and knee flexors and dorsiflexors.• Intensity adjusted based on tolerance • Monitor muscle response and patient comfort Tot Sit-to-stand, reaching, weight shifting, gait training, ball-kicking, tandem/side walking• Increase intensity by slightly reducing assistance • Add unstable surfaces for gait |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Fugl-Meyer Assessment:
Prazo: Baseline to 4 weeks
|
The Fugl-Meyer Assessment for Lower Extremity (FMA-LE) is a reliable tool to evaluate motor recovery in post-stroke patients.
It consists of 17 items divided into five sections: reflex activity, volitional movement within synergy, mixing synergies, movement with little or no synergy, and coordination/speed.
Each item is scored from 0 to 2, giving a maximum score of 34.
Higher scores indicate better motor function.
Reflex activity includes 3 items (max 6 points), synergy movements have 6 items (12 points), mixed synergy includes 2 items (4 points), isolated movements have 3 items (6 points), and coordination/speed includes 3 items (6 points).
The heel-to-shin test is used for coordination.
Scoring interpretation is: 0-10 severe, 11-20 moderate, 21-29 mild, and 30-34 minimal impairment.
It takes 20-30 minutes and is administered by a trained professional.
|
Baseline to 4 weeks
|
|
The Timed Up and Go (TUG) Test
Prazo: Baseline to 4 weeks
|
This is a quick and reliable assessment used to evaluate mobility, balance, and fall risk in older adults and patients with neurological conditions like stroke.
It involves timing how long it takes for a person to stand from a chair, walk three meters, turn, return, and sit down.
Times under 10 seconds indicate normal mobility, while over 30 seconds suggest high fall risk.
The test is simple, requires minimal equipment, and is widely used in clinical and rehabilitation settings.
It helps monitor patient progress and guides treatment planning.
|
Baseline to 4 weeks
|
|
10-Meter Walk Test
Prazo: Baseline to 4 weeks
|
The 10MWT is a quick and reliable assessment of gait speed over a short distance, commonly used in stroke rehabilitation.
It involves timing a patient when they walk a 10-m path, typically within a 14-m walkaway to account for acceleration and deceleration.
The test can be performed at a comfortable or fast pace.
Gait speed is calculated in meters per second and is considered a strong predictor of functional mobility, fall risk, and community ambulation.
It is widely used to monitor progress in stroke patients.
|
Baseline to 4 weeks
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Outros números de identificação do estudo
- REC/RCR & AHS/25/0211
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .