Investigating the Effect of Stochastic Resonance Vibration on Gait and Balance and Upper Extremity Function in Children With Cerebral Palsy
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Vibration devices have been used by some patients with cerebral palsy during therapy sessions. Researchers believe they have the potential to be even more useful for everyday use, and are doing this study to learn more about what they can do.
Participate in this study will be asked to complete assessments that test arm motion, muscle tone, motor control, and sensory function. They will then be asked to wear a wristband on each wrist and on their shoulder. These wristbands contain vibrators that can vibrate at different levels. The vibrations are caused by a low-level of sound waves that people may barely be able to hear. While wearing the vibration devices on the wrist and shoulder, participants will be asked to perform two tasks. The first task is called the box and blocks test, which consists of transferring wooden blocks from one box to another. The second test is called the Shriners upper extremity evaluation (SHUEE). In this test participants will perform a series of fine motor tasks with their hands. The SHUEE test will be video recorded for scoring by a study therapist at a later time on how much and how well participants use their impaired arm to perform the tasks. Participants will be asked to complete the box and blocks test and the SHUEE test 3 times. Participation in this study will be one single visit and last approximately an hour to an hour and a half.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Virginia
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Richmond, Virginia, États-Unis, 23298
- Virginia Commonwealth University
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Diagnosed with cerebral palsy
- 3 years to 18 years of age
- Able to reliably express pain, discomfort or fear as reported by the parent/guardian
- Manual ability classification scale (MACS) levels I, II or III
Exclusion Criteria:
- Any unstable medical condition. An unstable medical condition is a state of imminent threat to life such as shock, acute asthma, respiratory distress, severe infection and sepsis. Any patient in a clinic or therapy center presenting with signs and symptoms of an unstable medical condition will be directed to emergency medical services
Any medical condition preventing active rehabilitation reported by the parent/guardian such as:
o Thromboembolic disease, acute progressive neurological disorder, cardiovascular or pulmonary contraindications, aggressive behavior, severe cognitive deficits, joint instabilities and compromised bone health, recent or non-consolidated fractures, osteoporosis
- Subjects with cardiac pacemakers, electronic pumps or any other implanted medical devices
- Skin lesions affecting the areas where the device straps will be attached to the body
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Soins de soutien
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: stochastic resonance (SR) vibration
SR applied sub threshold at 90% of participant's detection threshold
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SR wraps will be applied to the one or both wrists depending on whether the impairment is unilateral or bilateral.
Two additional actuators will be secured around the shoulder.
The threshold for detection of SR will be determined by the examiner prior to initiating the test condition.
The intensity of the stimulation is adjustable with a scroll bar on the app and ranges from a 0 - 100.
The examiner will gradually increase the stimulus intensity until the participant reports being able to feel it.
This will set the participant's detection threshold.
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Comparateur factice: Sham treatment
SR devices worn but not turned on (0% of participant's detection threshold).
|
SR wraps will be applied to the one or both wrists depending on whether the impairment is unilateral or bilateral.
Two additional actuators will be secured around the shoulder.
The threshold for detection of SR will be determined by the examiner prior to initiating the test condition.
The intensity of the stimulation is adjustable with a scroll bar on the app and ranges from a 0 - 100.
The examiner will gradually increase the stimulus intensity until the participant reports being able to feel it.
This will set the participant's detection threshold.
|
|
Expérimental: Unblinded treatment
SR is applied above participant's detection threshold at a participant selected intensity.
|
SR wraps will be applied to the one or both wrists depending on whether the impairment is unilateral or bilateral.
Two additional actuators will be secured around the shoulder.
The threshold for detection of SR will be determined by the examiner prior to initiating the test condition.
The intensity of the stimulation is adjustable with a scroll bar on the app and ranges from a 0 - 100.
The examiner will gradually increase the stimulus intensity until the participant reports being able to feel it.
This will set the participant's detection threshold.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Manual Dexterity
Délai: Baseline to up to 1.5 hours
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Manual dexterity is will be assessed using the Box and Block (B&B) test.
The B&B test is scored by counting the number of blocks transferred during the 1 minute test.
Higher scores indicate better manual dexterity.
Change was assessed after each condition and compared to baseline.
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Baseline to up to 1.5 hours
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Change in Upper Extremity Functionality
Délai: Baseline to up to 1.5 hours
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Upper extremity functionality will be assessed using the Shriners Upper Extremity Evaluation (SHUEE).
Participants are observed and scored by a trained rater blind to the condition.
Scores range from 0 to 45 for spontaneous functional activity and from 0 to 72 for dynamic positional analysis.
Higher scores indicate better functionality.
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Baseline to up to 1.5 hours
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Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- HM20018459
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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