App-based Exercise Intervention for Persons With Acute Ankle Sprain
A Pilot Study Investigating the Use and Preliminary Effect of the App "Injury-map" in Providing Exercise Rehabilitation for Persons With Acute Lateral Ankle Sprains Seen at the Emergency Department - a Mixed-method Pilot Study
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Acute lateral ankle sprains (ALAS) account for 4-5% of all Emergency Department visits in Denmark and is the most common injury in sporting activities. It is often regarded as an innocuous injury but in truth up to 2/3 of individuals with a history of lateral ankle sprain have prolonged symptoms such as pain, decreased function and subjective instability for several years after their initial injury. Exercise therapy has proven to be a cost-effective rehabilitation in treating ALAS and in preventing re-injury. The financial modality of ALAS is high but exercise therapy has proven to be a cost-effective rehabilitation in treating ALAS and in preventing re-injury.
Modern technology has the potential to be a powerful tool in providing easily accessible exercise programs. Injury-map© is an exercise app designed for treating different musculoskeletal problems including ALAS. The exercise program has been developed by health professionals and has the potential to provide an easy-accessible management of ALAS rehabilitation. However, the app has currently not been tested in a clinical trial with patients suffering from ALAS. Before undertaking a large scale trial, the investigators wish to pilot test the app to assess the use and preliminary effect of the app-based exercise program.
This study aims to investigate the use and preliminary effect of an exercise program on a mobile device in patients with ALAS when seen in the Emergency Room at a public hospital. It is designed as a mixed method pilot cohort study. The SPIRIT checklist for trial protocols and the PREPARE trial guide have been used for the overall framework of this protocol.
Approximately 60 participants will be recruited from the Emergency Department (ED) at Hvidovre Hospital (HvH). Health specialists associated with the ED and responsible for ankle examinations will recruit participants . If a health specialist deems a person eligible, they will deliver a bag containing a rubber band and project description. If a participant is willing to participate in the project, they can contact the study administrator by the contact information in the written material. When contact is established participants will receive a voucher for the app, informed consent and a baseline questionnaire.
The exercise program will be available on any mobile device and/or tablet using Android or iOS. It is expected that patients primarily will exercise mainly at home. Participants will be followed as long as they actively use the exercise app or for a maximum of four months. When a participant has been inactive for more than two weeks, the participants are considered finalized and will be contacted for follow-up assessment.
Participants will receive a weekly SMS string where information of return to activity and subjective feeling of instability will be collected. The SMS string will send ever for four months. At follow-up assessment participants will receive a questionnaire containing questions of their experience with the exercise app. A number of participants will be selected to semi-structured interview to elaborate their user experience with the app. This selection will be based on the participants completion of exercises in the app. AT the ED and in the app system recruitment rates and adherence to the exercise program will be extracted.
Baseline characteristics will be summarized with suitable descriptive statistics.
For the aim of investigating the use of the App, adherence will be presented as the number of exercise sessions completed each week as well as average estimations. The results will be compared to an evidence-based exercise dose. Recruitment rates, retention rates will be presented in suitable descriptive tables. Any harms will be addressed individually.
Intervention outcomes will be summarized and tendencies in treatment effect will be compared with comparable literature, however no formal hypothesis testing will be performed, as the study uses a pilot design. Being an exploratory pilot study, the study is designed with a flat outcome structure with multiple evenly valued outcome measures.
Interviews will be recorded and transcribed verbatim. The data will be analysed using a thematic approach. The data will be coded and recurring phrases or words will be grouped into basic themes. These themes will be clustered into global themes which will be verified by comparison to the coded data [23]. Differences between participants who complete the intervention and those who do not will be discussed.
The enrollment process will start in April 2018 and conclude when 60 participants have been enrolled in the study.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Hvidove
-
Copenhagen, Hvidove, Dinamarca, 2650
- Hvidovre University Hospital
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Acute lateral ankle sprain (< 48 hours) evaluated by a relevant health specialist in the hospital Emergency department (HvH)
Exclusion Criteria:
- Fracture of the leg or foot (Ottawa rules and/or x-ray)
- Previous surgery in the ankle or as a consequence of the current ankle distortion.
- Other serious injury to the body in relation to the ankle injury incidence.
- Serious illness (terminal patients, RA, Fibromyalgia etc).
- Not having a smartphone or tablet.
- Unable to understand Danish.
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 |
|---|---|
|
Experimental: App-based exercise rehabilitation
Persons with Acute lateral ankle sprain (<48 hours) evaluated by a relevant health specialist in the hospital Emergency Department.
|
App-based exercise rehabilitation available on any mobile device and/or tablet using Android or iOS operating systems. The app Injurymap© is hosting the exercise program. The app requires user-registrations and a monthly paid subscription fee to access the exercise program. The participants in this study will not be charged for using the app. The exercise program consists of three phases with increasing difficulty. Each phase consists of several categories of exercise types. The categories are 1) mobility, 2) stability/balance, 3) strength and 4) stretching. Within each phase, there can be more than one exercise for each category. This makes it possible to adjust the difficulty of the exercises depending on user-feedback. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Return to work
Periodo de tiempo: Four months from ankle injury
|
Number of whole days absent from work due to the ankle injury
|
Four months from ankle injury
|
|
Return to sport
Periodo de tiempo: Four months from ankle injury
|
Number of exercise sessions not able to fully attend due to the ankle injury
|
Four months from ankle injury
|
|
Re-injuries in the same ankle
Periodo de tiempo: Four months from ankle injury
|
Total number of re-sprains categorized into two groups.
1) Ankle sprains with no time loss and 2) ankle sprains with time-loss defined as unable to continue current activity and/or unable to participate in work/sport activities the next days because of the ankle.
|
Four months from ankle injury
|
|
Subjective feeling of ankle stability
Periodo de tiempo: Every week from ankle injury until four months after
|
0-10 points, where 0 is completely stable and 10 is very unstable.
The participant writes a number within the indicated range that equates to their subjective feeling of stability.
|
Every week from ankle injury until four months after
|
|
Subjective feeling of recovery
Periodo de tiempo: Four months from ankle injury
|
Do you feel able to do the same activities on the same level as before the injury.
answer: YES or NO.
|
Four months from ankle injury
|
|
Recruitment rate: Number of potentially eligible participants at the Emergency Department
Periodo de tiempo: From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
|
Database search off registered ankle injuries at the Emergency Department in the recruitment period
|
From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
|
|
Recruitment rate: Number of persons contacted by the health specialist for information about the study
Periodo de tiempo: From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
|
Number of delivered recruitment bags containing project information and rubber bands by the health personel at the Emergency Department.
|
From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
|
|
Recruitment rate: Number of persons willing to participate.
Periodo de tiempo: From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
|
Number of participants who contacts the project administration for participation in the exercise project.
|
From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
|
|
Recruitment rate: Number of persons commencing the exercise program.
Periodo de tiempo: From start of recruitment to two weeks after the minimum of 60 participants has been achieved, but maximum 3 months and two weeks.
|
Number of participants included in the project who commence the exercise program.
|
From start of recruitment to two weeks after the minimum of 60 participants has been achieved, but maximum 3 months and two weeks.
|
|
Retention rate: Number of persons completing follow-up assessment.
Periodo de tiempo: Four months from ankle injury
|
The number of participants completing the four month follow-up questionnaire of the total number included participants.
|
Four months from ankle injury
|
|
Retention rate: Number of sms responded.
Periodo de tiempo: Four months from ankle injury
|
The number of sms responded of the total number of sms send.
|
Four months from ankle injury
|
|
Adherence to exercise program: Number of exercise sessions completed.
Periodo de tiempo: Four months from ankle injury
|
The number of sessions completed is extracted from the app database.
|
Four months from ankle injury
|
|
Adherence to exercise program: Number of weeks with minimum one exercise session.
Periodo de tiempo: Four months from ankle injury
|
The number of sessions completed in each week is extracted from the app database.
|
Four months from ankle injury
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
semi-structured interviews
Periodo de tiempo: two weeks after ended intervention but maximum 4 months and two weeks after the initial ankle injury.
|
To uncover user experiences with the app-based exercise program.
|
two weeks after ended intervention but maximum 4 months and two weeks after the initial ankle injury.
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Jonas Bak, MSc, Hvidovre University Hospital
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
- 17041467
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. .