Telerehabilitation of Patients After Knee Surgery
Future Patient - Telerehabilitation of Patients After Knee Surgery
This project is aimed to investigate the feasibility of employing communication and sensor technologies for the patient after a knee operation.
In the study, it is hypothesized that the effectiveness of postoperative rehabilitation programs might be improved by establishing electronic communication between healthcare professionals and the patients. It is also believed that users satisfaction and patients quality of life will be improved.
The telerehabilitation program promises a synchronized communication as well as an individualized training program (by health professionals) based on the patient's electronic reports.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Aim The objectives of this project are to assess the feasibility of using a telerehabilitation program for patients after a knee operation and investigate the acceptance of the provided solution by the patients and healthcare professionals.
Hypothesis It is hypothesized that the acceptance and satisfaction of patients and healthcare professionals by using the telerehabilitation program will be high and correlated with patients' exercise adherence and health recovery.
Telerehabilitation Group (Target Group) The subjects will be recruited before the operation and will be followed during an 8-week rehabilitation period.
In addition to the telerehabilitation program, the subjects will receive the regular treatment offered by Farsø Hospital in connection with total knee replacement surgery and are to follow the same rehabilitation procedure as regular patients (see below).
Before the operation, the project physiotherapist will hand over the telerehabilitation system equipment and instruct the subject how to use the system. In addition, the physiotherapist will also ask the subject to follow the instruction process and try the available services a few times. The physiotherapist makes sure that the subject can operate the system easily and without any challenges.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Aalborg, Dinamarca, 9220
- Aalborg University
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Farsø, Dinamarca, 9640
- Aalborg University Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Aged over 18
- Successful primary total knee replacement surgery at Farsø Hospital
- Referred to the regular rehabilitation program (self-training at home) by the physiotherapists at Farsø Hospital
- Ability to walk (with or without walking aids)
- Able to use electronic technologies and devices (for example: smart phone, tablet) or at least one relative who can assist in this matter
- Living in The North Denmark Region
Exclusion Criteria:
- Previous or current drug addiction defined as the use of cannabis, opioids or other drugs
- Previous or current neurologic, musculoskeletal or mental illnesses
- Any other aggravating medical complication (such as infection or DVT)
- Lack of ability to understand and accept trial procedures
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Intervention group
The patient assign to this arm receive the telerehabilitation program for 8-week after a knee operation
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The telerehabilitation program equipment consists of the following devices:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Usability of the telerehabilitation program: semi-structured interview
Periodo de tiempo: The interview is conducted two weeks after discharge.
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The data is collected by a semi-structured interview
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The interview is conducted two weeks after discharge.
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Exercise adherence
Periodo de tiempo: Everyday, started after discharge and for period of 8-weeks
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Measured by telerehabilitation system reports
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Everyday, started after discharge and for period of 8-weeks
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Self-reported pain, stiffness, and physical function: KOOS
Periodo de tiempo: After discharge (weeks 2, 8)
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Measured using Knee injury and Osteoarthritis Outcome Score (KOOS)
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After discharge (weeks 2, 8)
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Self-reported pain and physical function: OKS
Periodo de tiempo: Baseline (before operation), and after discharge (weeks 0,2,4,6,8)
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measured by an electronic version of Oxford Knee Score (OKS)
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Baseline (before operation), and after discharge (weeks 0,2,4,6,8)
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Self-reported pain: VAS
Periodo de tiempo: Baseline (before operation), and every third day after discharge (for period of 8 weeks)
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Measured by an electronic report of the visual analog scale (VAS) of pain [minimum 0, Maximum 10] higher values represent a higher level of pain
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Baseline (before operation), and every third day after discharge (for period of 8 weeks)
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Self-reported knee swelling
Periodo de tiempo: Baseline (before operation), and every third day after discharge (for period of 8 weeks)
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measured by an electronic report of knee circumference
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Baseline (before operation), and every third day after discharge (for period of 8 weeks)
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Quality of life: EQ-5D
Periodo de tiempo: After discharge (weeks 2, 8)
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Measured using Euro Quality of Life - 5 Dimension (EQ-5D)
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After discharge (weeks 2, 8)
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Users satisfaction: semi-structured interview
Periodo de tiempo: The interview is conducted two weeks after discharge.
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Measured by semi-structured interview
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The interview is conducted two weeks after discharge.
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Colaboradores e Investigadores
Patrocinador
Colaboradores
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
- N-20180012
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan 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.
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Ensayos clínicos sobre Telerehabilitation
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Akdeniz UniversityAún no reclutandoAccidente cerebrovascular isquémico | EntrenamientoPavo