Use of Wearable Tech to Increase Physical Activity in Inpatient Rehabilitation for Patients With Chronic Pain
Descripción general del estudio
Estado
Condiciones
Descripción detallada
Chronic pain is a vast problem with profound consequences for individuals and societies. Exercise and physical activity is an important part of the treatment for chronic pain. Use of wearable tech might be a way to help facilitate physical activity in patients with chronic pain. Here it will be evaluated whether use of wearable tech giving feedback about the user's activity level increases physical activity in patients participating in inpatient rehabilitation for chronic pain. The control group will be wearing the same wearable tech as the intervention group, but they will not receive any feedback about their activity level.
The feedback application will give participants in the intervention group information about the number of PAI they earn each week. PAI is short for personal activity Intelligence. You earn PAI points every time your heart rate increases: The higher heart rate, the faster you earn PAI. Previous research have shown that those who achieve 100 PAI or more every week over time live for an average of more than eight years longer than others.
During the study all participants will take part in a traditional inpatient rehabilitation program. The program consist of two periods at the rehabilitation center with two weeks at home in-between. The study will take place during the two periods at the senter and the period at home. Time spent on physical activity and number of earned PAI's will be counted during the period at home.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Rissa, Noruega
- Unicare Helsefort
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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:
- taking part in inpatient rehabilitation at Unicare Helefort Rehabilitation center for chronic pain.
Exclusion Criteria:
- not having a smartphone (will not be able to access the mobile application).
- using a wheelchair (the technology will be not able to measure activity correctly)
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Comparador activo: Tecnología portátil sin retroalimentación
Este grupo usará el mismo dispositivo de medición de actividad que el grupo de intervención, pero no recibirá ningún comentario sobre su nivel de actividad.
No tendrán acceso a la aplicación móvil.
Participarán en el mismo programa de rehabilitación que el grupo de intervención.
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traditional inpatient rehabilitation program.
An armwrist device measuring physical activity level, no reporting back to the user.
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Experimental: Wearable tech with feedback
This group will be wearing an activity measurement device (wristband) and receive feedback about their activity level through a mobile application while taking part in a traditional inpatient rehabilitation program for patients with chronic pain.
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An armwrist device measuring physical activity level.
The user will receive information about their physical activity level through their smartphone.
traditional inpatient rehabilitation program.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Activity level
Periodo de tiempo: 2 weeks (time period at home between two stays at the rehabilitation center)
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Time spent in moderate to vigorous physical activity (minutes per day)
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2 weeks (time period at home between two stays at the rehabilitation center)
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Number of PAIs
Periodo de tiempo: 2 weeks (time period at home between two stays at the rehabilitation center)
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mean number of Personal Activity Intelligence (PAI) points achieved per week
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2 weeks (time period at home between two stays at the rehabilitation center)
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Percentage achieving 100 PAIs per week
Periodo de tiempo: 2 weeks (time period at home between two stays at the rehabilitation center)
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Personal Activity Intelligence (PAI)
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2 weeks (time period at home between two stays at the rehabilitation center)
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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oxygen uptake
Periodo de tiempo: 6 weeks (from inclusion to end of rehabilitation program)
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submaximal oxygen uptake measured by the Åstrand bicycle test (described in Textbook of work physiology by Astrand from 1986)
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6 weeks (from inclusion to end of rehabilitation program)
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Anxiety and depression symptoms
Periodo de tiempo: 6 weeks (from inclusion to end of rehabilitation program)
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HSCL-25 questionnaire
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6 weeks (from inclusion to end of rehabilitation program)
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Average pain
Periodo de tiempo: 6 weeks (from inclusion to end of rehabilitation program)
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Visual Analogue Scale (VAS).
VAS is a straight horizontal line where the ends are defined as the extreme limits from the left (0-no pain) to the right (100-worst imaginable pain).
The patient is asked to mark his pain level on the line between the two endpoints.
The distance between 'no pain at all' and the mark then defines the subject's pain.
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6 weeks (from inclusion to end of rehabilitation program)
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Health related quality of life
Periodo de tiempo: 6 weeks (from inclusion to end of rehabilitation program)
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EQ5D questionnaire
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6 weeks (from inclusion to end of rehabilitation program)
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Body weight
Periodo de tiempo: 6 weeks (from inclusion to end of rehabilitation program)
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body weight in kilograms
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6 weeks (from inclusion to end of rehabilitation program)
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Body Mass Index score
Periodo de tiempo: 6 weeks (from inclusion to end of rehabilitation program)
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weight in kilograms divided by height in metres squared
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6 weeks (from inclusion to end of rehabilitation program)
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Lene Aasdahl, PhD MD, National Taiwan Normal University
- Director de estudio: Jorunn Helbostad, Dr Philos, Norwegian University of Science and Technology
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
- 2019/800
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.
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