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- Ensaio Clínico NCT07654582
Effect of Adding Augmented Cues /Hand Stroke Patient (AUGMENTED CUES)
Effect of Adding Augmented Cues to Physical Therapy Intervention on Hand Function Post Stroke Patients
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Stroke is one of the leading causes of long-term disability worldwide and frequently results in impaired hand function, reduced dexterity, decreased grip strength, and limitations in activities of daily living. Conventional physical therapy is commonly used to improve upper extremity function; however, recovery of hand performance remains challenging for many stroke survivors.
Augmented cues provide additional sensory information through visual, auditory, or sensorimotor feedback that may enhance motor learning and neuroplasticity. Incorporating augmented cues into rehabilitation programs may improve patient engagement, increase repetition of task-specific movements, and facilitate functional recovery.
The purpose of this randomized controlled trial is to examine the effectiveness of adding augmented cue-based training to conventional physical therapy intervention in improving hand function among patients with subacute ischemic stroke.
A total of 50 participants meeting the eligibility criteria will be recruited and randomly assigned into two equal groups:
Study Group: Participants will receive augmented cue-based training combined with conventional physical therapy.
Control Group: Participants will receive conventional physical therapy only.
The intervention will be conducted over an eight-week treatment period. Outcome measures will be collected before and after treatment and will include:
- Nine-Hole Peg Test (NHPT) to assess manual dexterity.
- Hand grip strength measured using a hand dynamometer.
- Pressure pain threshold measured using a pressure algometer.
The primary objective is to determine whether the addition of augmented cues results in greater improvement in hand function compared with conventional physical therapy alone. The results may contribute to the development of more effective rehabilitation strategies for individuals recovering from stroke.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
- Nome: Mostafa abdullah ahmed, MD
- Número de telefone: 00201095052373
- E-mail: dr.mostafa.abdullah.abdelaziem@gmail.com
Estude backup de contato
- Nome: mariam mohamed elsayed, phd
- Número de telefone: 002010950505529
- E-mail: mariamelanany5@gmail.com
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- - Male and female patients.
- Age between 40 and 60 years.
- First-ever subacute ischemic stroke.
- Time since stroke between 6 weeks and 6 months.
- Unilateral upper limb involvement.
- Able to understand and follow verbal instructions.
- Medically stable and able to participate in the rehabilitation program.
- Willing to provide informed consent.
Exclusion Criteria:
- - Hemorrhagic stroke.
- Bilateral stroke involvement.
- Severe cognitive impairment or severe aphasia interfering with participation.
- Severe visual or auditory deficits affecting training.
- Severe upper limb spasticity that prevents hand training.
- Other neurological disorders affecting upper limb function.
- Severe musculoskeletal disorders of the upper limb.
- Participation in another rehabilitation trial during the study period.
- Unstable cardiovascular or medical conditions.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Comparador Ativo: control group
Participants will receive a conventional physical therapy program for hand rehabilitation after stroke.
Treatment will be administered three times per week for eight weeks (24 sessions), with each session lasting 60 minutes and including range of motion exercises, strengthening exercises, stretching, and task-oriented hand training.
|
Participants will receive a conventional physical therapy program for upper limb and hand rehabilitation after stroke.
The program includes stretching exercises, range of motion exercises, strengthening exercises, and task-oriented hand training.
Treatment will be provided three times per week for eight weeks (24 sessions).
|
|
Experimental: musical gloves
articipants will receive the same conventional physical therapy program provided to the control group in addition to MusicGlove training.
Treatment will be administered three times per week for eight weeks (24 sessions).
MusicGlove will provide augmented visual, auditory, and performance feedback during task-specific hand training.
|
Participants will receive a conventional physical therapy program for upper limb and hand rehabilitation after stroke.
The program includes stretching exercises, range of motion exercises, strengthening exercises, and task-oriented hand training.
Treatment will be provided three times per week for eight weeks (24 sessions).
MusicGlove is a sensor-based rehabilitation device that provides augmented visual, auditory, and performance feedback during task-specific hand exercises.
Participants perform repetitive thumb-to-finger opposition and grasping movements synchronized with computer-based musical activities.
Training will be provided in addition to conventional physical therapy three times per week for eight weeks.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Nine-Hole peg Test (NHPT)
Prazo: Baseline and after 8 weeks of treatment
|
Manual dexterity assessed using the Nine-Hole Peg Test.
The time required to place and remove nine pegs will be recorded in seconds.
Lower scores indicate better hand dexterity.
|
Baseline and after 8 weeks of treatment
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
hand grip strength
Prazo: Baseline and after 8 weeks of treatment
|
Hand grip strength will be assessed using a calibrated hand dynamometer.
Participants will perform maximal voluntary grip contractions, and the average value of three trials will be recorded in kilograms.
Higher values indicate greater hand strength.
|
Baseline and after 8 weeks of treatment
|
|
pressure pain threshold
Prazo: Baseline and after 8 weeks of treatment
|
Pressure pain threshold of the Extensor Carpi Radialis Brevis muscle will be measured using a digital pressure algometer.
Pressure will be applied at a standardized rate until the participant first perceives pain.
Higher values indicate lower pain sensitivity.
|
Baseline and after 8 weeks of treatment
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Cadeira de estudo: Moshera H Darwish, PHD, Professor of Physical Therapy for Neurology and Neurosurgery Faculty of Physical Therapy Cairo University
- Diretor de estudo: mariam m elsayed, phd, Lecturer in department of physical Therapy for Neurology and Neurosurgery Faculty of physical therapy Cairo University
- Diretor de estudo: Essam M Abdulwahab, PHD, Professor of Neurology Faculty of Medicine Al-Azhar university
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
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
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- P.T.REC/012/006310
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Descrição do plano IPD
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