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App-based Exercise Intervention for Persons With Acute Ankle Sprain

Primary Purpose

Ankle Sprains

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
App-based exercise rehabilitation
Sponsored by
Hvidovre University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ankle Sprains focused on measuring Acute lateral ankle sprain, Acute ankle injury, Ankle sprain, Exercise therapy, App-based rehabilitation, Mixed-method, Pilot Study

Eligibility Criteria

5 Years - 120 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Hvidovre University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

App-based exercise rehabilitation

Arm Description

Persons with Acute lateral ankle sprain (<48 hours) evaluated by a relevant health specialist in the hospital Emergency Department.

Outcomes

Primary Outcome Measures

Return to work
Number of whole days absent from work due to the ankle injury
Return to sport
Number of exercise sessions not able to fully attend due to the ankle injury
Re-injuries in the same ankle
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.
Subjective feeling of ankle stability
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.
Subjective feeling of recovery
Do you feel able to do the same activities on the same level as before the injury. answer: YES or NO.
Recruitment rate: Number of potentially eligible participants at the Emergency Department
Database search off registered ankle injuries at the Emergency Department in the recruitment period
Recruitment rate: Number of persons contacted by the health specialist for information about the study
Number of delivered recruitment bags containing project information and rubber bands by the health personel at the Emergency Department.
Recruitment rate: Number of persons willing to participate.
Number of participants who contacts the project administration for participation in the exercise project.
Recruitment rate: Number of persons commencing the exercise program.
Number of participants included in the project who commence the exercise program.
Retention rate: Number of persons completing follow-up assessment.
The number of participants completing the four month follow-up questionnaire of the total number included participants.
Retention rate: Number of sms responded.
The number of sms responded of the total number of sms send.
Adherence to exercise program: Number of exercise sessions completed.
The number of sessions completed is extracted from the app database.
Adherence to exercise program: Number of weeks with minimum one exercise session.
The number of sessions completed in each week is extracted from the app database.

Secondary Outcome Measures

Full Information

First Posted
May 1, 2018
Last Updated
November 11, 2019
Sponsor
Hvidovre University Hospital
Collaborators
Copenhagen Center for Health Technology (CACHET), Technical University of Denmark (DTU)
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1. Study Identification

Unique Protocol Identification Number
NCT03550274
Brief Title
App-based Exercise Intervention for Persons With Acute Ankle Sprain
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
July 3, 2018 (Actual)
Primary Completion Date
August 3, 2019 (Actual)
Study Completion Date
August 3, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hvidovre University Hospital
Collaborators
Copenhagen Center for Health Technology (CACHET), Technical University of Denmark (DTU)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Acute lateral ankle sprains (ALAS) account for 4-5% of all Emergency Department visits in Denmark. Up to 2/3 of individuals with a history of lateral ankle sprain have prolonged symptoms 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. Injury-map© is an exercise app designed for treating different musculoskeletal problems including ALAS. The app has currently not been tested in a clinical trial with patients suffering from ALAS. This mixed method pilot cohort study aims to investigate the use and preliminary effect of an exercise program on a mobile device in patients with ALAS. The exercise program is designed to be completed within approximately 3 months. However, participants will be followed as long as they complete minimum 1 exercise session per week. If a participant is inactive for two weeks they will be considered completed and contacted for follow-up assessment.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankle Sprains
Keywords
Acute lateral ankle sprain, Acute ankle injury, Ankle sprain, Exercise therapy, App-based rehabilitation, Mixed-method, Pilot Study

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Mixed method pilot cohort study
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
App-based exercise rehabilitation
Arm Type
Experimental
Arm Description
Persons with Acute lateral ankle sprain (<48 hours) evaluated by a relevant health specialist in the hospital Emergency Department.
Intervention Type
Device
Intervention Name(s)
App-based exercise rehabilitation
Intervention Description
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.
Primary Outcome Measure Information:
Title
Return to work
Description
Number of whole days absent from work due to the ankle injury
Time Frame
Four months from ankle injury
Title
Return to sport
Description
Number of exercise sessions not able to fully attend due to the ankle injury
Time Frame
Four months from ankle injury
Title
Re-injuries in the same ankle
Description
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.
Time Frame
Four months from ankle injury
Title
Subjective feeling of ankle stability
Description
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.
Time Frame
Every week from ankle injury until four months after
Title
Subjective feeling of recovery
Description
Do you feel able to do the same activities on the same level as before the injury. answer: YES or NO.
Time Frame
Four months from ankle injury
Title
Recruitment rate: Number of potentially eligible participants at the Emergency Department
Description
Database search off registered ankle injuries at the Emergency Department in the recruitment period
Time Frame
From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
Title
Recruitment rate: Number of persons contacted by the health specialist for information about the study
Description
Number of delivered recruitment bags containing project information and rubber bands by the health personel at the Emergency Department.
Time Frame
From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
Title
Recruitment rate: Number of persons willing to participate.
Description
Number of participants who contacts the project administration for participation in the exercise project.
Time Frame
From start of recruitment to the minimum of 60 participants has been achieved, but maximum 3 months
Title
Recruitment rate: Number of persons commencing the exercise program.
Description
Number of participants included in the project who commence the exercise program.
Time Frame
From start of recruitment to two weeks after the minimum of 60 participants has been achieved, but maximum 3 months and two weeks.
Title
Retention rate: Number of persons completing follow-up assessment.
Description
The number of participants completing the four month follow-up questionnaire of the total number included participants.
Time Frame
Four months from ankle injury
Title
Retention rate: Number of sms responded.
Description
The number of sms responded of the total number of sms send.
Time Frame
Four months from ankle injury
Title
Adherence to exercise program: Number of exercise sessions completed.
Description
The number of sessions completed is extracted from the app database.
Time Frame
Four months from ankle injury
Title
Adherence to exercise program: Number of weeks with minimum one exercise session.
Description
The number of sessions completed in each week is extracted from the app database.
Time Frame
Four months from ankle injury
Other Pre-specified Outcome Measures:
Title
semi-structured interviews
Description
To uncover user experiences with the app-based exercise program.
Time Frame
two weeks after ended intervention but maximum 4 months and two weeks after the initial ankle injury.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
120 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonas Bak, MSc
Organizational Affiliation
Hvidovre University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hvidovre University Hospital
City
Copenhagen
State/Province
Hvidove
ZIP/Postal Code
2650
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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App-based Exercise Intervention for Persons With Acute Ankle Sprain

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