Use of Rhythmic Auditory Cueing During Bilateral Training of the Upper Extremities in Stroke Patients
Przegląd badań
Status
Warunki
Szczegółowy opis
Arm and hand movement problems are major contributors to disability in patients after stroke. In fact, only 5% of adults regain full arm function after stroke, and 20% regain no functional use. Hence, alternative strategies are needed to reduce the long-term disability and functional impairment from upper limb hemiparesis.
To solve problems concerning upper limb dysfunction related to stroke, various treatment methods have been used in several previous studies. Rhythmic auditory stimulation has been reported as an effective intervention for improving movement in the affected extremities of stroke patients.
To the best of our knowledge, no mentioned previous studies evaluating the effect of rhythmic auditory cueing with bilateral arm training using functional exercises on upper extremity impairment in patients with stroke in Egypt are reported. So, this study aims to determine the effect of rhythmic auditory cueing with bilateral arm training on upper limb functions in patients with stroke.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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Dokki, Egipt
- Outpatient clinic - Faculty of Physical Therapy - Cairo University
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Thirty patients with ischemic stroke from both sexes will be included.
- Patients will have stroke for the first time.
- The age of patients will range from 45 to 60 years.
- Duration of illness will be from six months to eighteen months.
- The degree of spasticity will ranged from 1 to 1 + grade according to the modified Ashworth scale.
- Patients will have moderate arm motor impairment (between 30 and 49 scores) according to Fugl-Meyer (FM) arm section scale.
- The affected upper extremity will be the dominant side.
- Patients will be able to sit and maintain balance in a sitting position.
Exclusion Criteria:
The patients will be excluded if they have:
- Visual or auditory deficits.
- Perceptual disorders.
- Any surgical interventions in the upper extremities limiting the range of motion.
- Aphasia or apraxia.
- Musculoskeletal or neurological impairment of the unaffected upper extremity.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Podwójnie
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Rhythmic Auditory Cueing
Group (B): Patients in this group will receive the same designed physical therapy program given to the control group in addition to auditory cueing during bilateral arm training using the metronome.
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Patients will perform the same movement sequence in time with the metronome beat. The frequency of the rhythmic auditory stimulation will be matched to the participant"s preferred movement speed, which will be assessed prior to the start of the trial, and participants typically started moving after they had heard the metronome beat two to three times. Participants will be given sufficient practice trials to ensure full understanding before the actual recording of data, and will be given 3-minutes break between trials. On the 3rd and 5th week, the rhythm frequency was increased by 5%.
Training will consist of 20 minutes of bilateral arm training In each session, patients will be seated comfortably at a table in the following limb positions: ankles in neutral dorsiflexion, knees and hips placed at 90°, shoulders in 0° flexion, elbows in 60° flexion, and wrists in neutral position of flexion/extension
Scapular mobilization.
Thoracic spine mobilization.
Mechanical assisted (active and passive) exercises.
Therapeutic positioning as weight bearing on the paretic arm.
Opening and closing closed fist.
Strengthening exercise.
Stretching of spastic muscles.
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Aktywny komparator: Bilateral arm training
Patients in this group will receive a standard physical therapy program in addition to Bilateral arm training.
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Training will consist of 20 minutes of bilateral arm training In each session, patients will be seated comfortably at a table in the following limb positions: ankles in neutral dorsiflexion, knees and hips placed at 90°, shoulders in 0° flexion, elbows in 60° flexion, and wrists in neutral position of flexion/extension
Scapular mobilization.
Thoracic spine mobilization.
Mechanical assisted (active and passive) exercises.
Therapeutic positioning as weight bearing on the paretic arm.
Opening and closing closed fist.
Strengthening exercise.
Stretching of spastic muscles.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Assessing the change in Upper Extremity Motor Performance
Ramy czasowe: Baseline and 6 weeks post-intervention
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Assessment via using Upper Extremity Motor Performance scale.
This scale has been shown to be valid and reliable, and it correlates well with inter joint upper extremity coordination.
It has a maximum score of 66
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Baseline and 6 weeks post-intervention
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Assessing the change in upper limb Motor Function
Ramy czasowe: Baseline and 6 weeks post-intervention
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Assessment via using Wolf Motor Function Test (WMFT) The final time score will be the median time required for all timed tasks executed.
One hundred twenty seconds is the maximum time allowed for each task attempted Timing is carried out using a stopwatch.
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Baseline and 6 weeks post-intervention
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Assessing the change in gross manual dexterity
Ramy czasowe: Baseline and 6 weeks post-intervention
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Assessment via using Box and Block Test Involves moving 1-inch cube blocks from a rectangular box container to another container, and the number of blocks moved by each hand in 60 seconds is determined using stop watch
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Baseline and 6 weeks post-intervention
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Współpracownicy i badacze
Sponsor
Śledczy
- Główny śledczy: Reem Abdelhady, Cairo University
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- Reem_MSc
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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