- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04825405
The Use of the Tip Stim Glove Device to Achieve Coordinated Movement of the Human Hand
Influence of the Tested Position and the Use of the TipStim Glove Device on the Improvement of the Hand Motor Coordination After Stroke
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
To test the effectiveness of the Tip Stim device, each patient received (alternating) both the experimental and control treatments in a specific sequence to assess the coordination of human hand movement and the grip strength. The first therapy with the use of Tip Stim parameters (Ratio current time to pause time: 2 sec :5 sec; Ramp (rise time impulse): 0,3 sec; Frequency: 20 Hz; Pulse width: 300 µs). Another session (putting on the glove without setting any parameters) took place after a week (time to mute the effects of the intervention). The duration of each therapy session is 60 minutes. After the first therapeutic session and after a week, the parameters of movement coordination and hand grip were examined. The study of motor coordination and grip strength was performed in two different starting positions: sitting (no stabilization) (fig. 1) and lying (with stabilization) (fig. 2), and with a different position of the examined upper limb. During the first examination, the subject sat on a treatment table, feet resting on the floor. Upper limb examined in adduction, with bent elbow joint in the intermediate position between pronation and supination of the forearm. In the supine examination, the upper limb was stabilized against the subject's body (adduction in the shoulder joint, flexion in the elbow joint in an intermediate position). In each of the starting positions, first after putting on the glove, the range of passive motion in the radial-wrist joint (flexion and extension) and fingers (global flexion and extension) was measured, then the active movement was measured, in the sequence as above. Eventually, they were asked to make movements as quickly and as fully as possible. Measurement of the grip force with a dynamometer was performed in both analyzed starting positions after testing the ranges of motion and speed/frequency.
The Hand Tutor device and the EH 101 electronic hand dynamometer measuring the strength of the handgrip (measurement error 0.5 kg / 1 lb) were used to test the parameters of motor coordination and grip strength. The Hand Tutor is a device with a rehabilitation program and the ability to measure the range of passive and active movement, deficits of movement (error of measurement, 5 - 10 mm) as well as the speed/frequency of movement (error of measurement, 0,5 cycle/sec.).
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Masovian District
-
Warsaw, Masovian District, Polonia, 04-141
- Anna Olczak
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:: 1) patients with hemiparesis after 5 to 7 weeks after stroke; 2) no severe deficits in communication, memory, or understanding what can impede proper measurement performance; 3) at least 40 years of age; 4) maximum 89 years of age.
-
Exclusion Criteria:1) stroke up to two weeks after the episode, 2) acute polyneuropathy and damage to peripheral nerves, 3) lack of trunk stability, 4) no wrist and hand movement, 5) hypersensitivity to electrical stimulation, 6) metal implants in the hand, cardiac dysfunction, epilepsy, 7) decorations on the fingers, 8) high or very low blood pressure, 9) dizziness , malaise of the respondents.
-
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador activo: The use of the active Tip Stim device to achieve coordinated of the hand.
Influence of the tested position and the use of the active TipStim Glove device on the improvement of motor coordination and grip force in patients after a stroke.
|
The next therapy with the use of Tip Stim took place after a week.
The duration of each therapy session was 60 minutes.
After the first therapy session and after a week, the parameters of movement coordination and handgrip were examined.
The study of motor coordination and grip strength was performed in two different starting positions: sitting (no stabilization) and lying (with stabilization), and with a different position of the examined upper limb.
The upper limb was examined in adduction, with the bent elbow joint in the intermediate position of the forearm.
In each of the starting positions, first, the range of passive motion in the wrist joint (flexion and extension) and fingers (global flexion and extension) was measured, then the active movement was measured, in the sequence as above.
Patients were asked to make movements as quickly and as fully as possible.
Measurement of the grip force was performed after testing the ranges of motion and speed/frequency.
Otros nombres:
|
|
Comparador de placebos: The use of the passive Tip Stim device to achieve coordinated of the hand.
Influence of the tested position and the use of the passive TipStim Glove device on the improvement of motor coordination and grip force in patients after a stroke.
|
The next therapy with the use of Tip Stim took place after a week.
The duration of each therapy session was 60 minutes.
After the first therapy session and after a week, the parameters of movement coordination and handgrip were examined.
The study of motor coordination and grip strength was performed in two different starting positions: sitting (no stabilization) and lying (with stabilization), and with a different position of the examined upper limb.
The upper limb was examined in adduction, with the bent elbow joint in the intermediate position of the forearm.
In each of the starting positions, first, the range of passive motion in the wrist joint (flexion and extension) and fingers (global flexion and extension) was measured, then the active movement was measured, in the sequence as above.
Patients were asked to make movements as quickly and as fully as possible.
Measurement of the grip force was performed after testing the ranges of motion and speed/frequency.
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Range of passive movement of the wrist, mm
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the range of passive movement (in mm)
|
up to 1 week
|
|
Range of active movement of the wrist, mm
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the range of active movement (in mm)
|
up to 1 week
|
|
Wrist extension deficit, mm
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the wrist extension deficit, (in mm)
|
up to 1 week
|
|
Wrist flexion deficit, mm
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the wrist flexion deficit, (in mm)
|
up to 1 week
|
|
Maximum range of wrist movement
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the maximum range of movement (in mm)
|
up to 1 week
|
|
Frequncy of wrist movement (flexion to extension), cycle#sec
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measurement of the speed or frequency (i.e., the number of cycles per sec.)
|
up to 1 week
|
|
Assessment of the grip strength
Periodo de tiempo: up to 1 week
|
A manual electronic dynamometer (EH 101) was used for grip strength measurement (kg)
|
up to 1 week
|
|
Range of passive movement of the fingers, mm
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the range of fingers passive movement (in mm)
|
up to 1 week
|
|
Range of active movement of the fingers, mm
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the range of fingers active movement (in mm)
|
up to 1 week
|
|
Fingers extension deficit, mm
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the fingers extension deficit, (in mm)
|
up to 1 week
|
|
Fingers flexion deficit, mm
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the fingers flexion deficit, (in mm)
|
up to 1 week
|
|
Maximum range of fingers movement
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measuremnt of the maximum range of movement (in mm)
|
up to 1 week
|
|
Frequncy of fingers movement (flexion to extension), cycle#sec
Periodo de tiempo: up to 1 week
|
The Hand Tutor allows measurement of the speed or frequency (i.e., the number of cycles per sec.)
|
up to 1 week
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Anna Olczak, PhD, Military Institute of Medicine
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 6/KRN/2019
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .