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The Effect of Activity Feedback Enabled by Smart Watches During In-patient Stroke Rehabilitation

Primary Purpose

Stroke

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Feedback against tailored target
No feedback
Sponsored by
The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Admission for acute/sub-acute in-patient neurorehabilitation of a first stroke at the 2nd affiliated hospital of Anhui University of Traditional Medicine and Acupuncture, Hefei, China.
  • Time from onset of stroke to admission for rehabilitation <16 weeks.
  • Ability to follow a two stage command; pick up an object, put object on table.
  • Independent in mobility prior to admission. Subjects can use any type of assistive device and brace needed.
  • Able to understand and repeat information related to the Informed Consent.

Exclusion Criteria:

  • Admission for second stroke.
  • Subjects who are unable to provide consent due to a cognitive impairment.

Sites / Locations

  • The 2nd Affiliated Hospital to Anhui University of Tranditional Chinese MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Feedback against tailored target

No Feedback

Arm Description

For each two hour epoch, the watch calculate the level of activity for the same epoch the day before, and adds 5% as the new target to be achieved.

For participants assigned to the control group, the smart watch will not provide any activity feedback against a target; it simply shows which two hour epoch a person is in.

Outcomes

Primary Outcome Measures

Change in activity counts as measured by a triaxial accelerometer from a smart watch from admission to 3 weeks or discharge from rehabilitation

Secondary Outcome Measures

Activity goal attainment as measured and provided by the smart watch
Participants in feedback group receive a preset activity goal based on their previous activity levels at baseline. The smart watch will then provide graduated encouragement by increasing their activity goal by about 5%. Every 10-15 minutes the screen lights up and participants can see their activity progress expressed by activity bars (representing 0-100%). Participants reaching their activity goal is used to measure goal attainment.
Change in walking mobility
Change in walking speed and spatio-temporal characteristics of walking as measured by an inertial sensor on the lower trunk during a 10m walk test.
Fatigue
Fatigue Severity Index
Health status on EQ-5D-5L
This scale is used a measure for health status and compromises 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression
Change in functional mobility as measured by Rivermead Mobility Index (RMI)
This scale assesses functional mobility in gait, balance and transfers after stroke
Change in cognitive function as measured by The Montreal Cognitive Assessment (MoCA)
This is a screening instrument for to measure mild cognitive dysfunction. It assesses different cognitive domains: attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation.
Change in arm function recovery
Grip dynamometer
Change in performance of activities of daily living as measured by Barthel ADL Index
This scale is used to record what the participant undertakes in personal activities, to establish a degree of independence from any help, physical or verbal.
Change in disability as measured by WHO Disability Assessment Scale (12 item version)
This scale provides a global measure of disability covering 6 domains: cognition, mobility, self-care, getting along, life activities, and participation
Adverse events
Self-reported adverse events

Full Information

First Posted
September 30, 2015
Last Updated
April 20, 2017
Sponsor
The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Collaborators
Oxford Brookes University, Oxford International Rehabilitation Foundation and Innovation, University of Warwick
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1. Study Identification

Unique Protocol Identification Number
NCT02587585
Brief Title
The Effect of Activity Feedback Enabled by Smart Watches During In-patient Stroke Rehabilitation
Official Title
An International Randomized Clinical Trial of Activity Feedback During In-patient Stroke Rehabilitation Enabled by Smart Watches
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (undefined)
Primary Completion Date
January 2018 (Anticipated)
Study Completion Date
August 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Collaborators
Oxford Brookes University, Oxford International Rehabilitation Foundation and Innovation, University of Warwick

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The amount of activity completed by individuals within rehabilitation programs, even when units are well staffed, is often far below that required for optimal stroke rehabilitation, and is not individually adapted on a day-to-day basis. Daily feedback on their activity levels may motivate stroke survivors to engage in greater skills practice and thus outcome after stroke. To date only a few trials suggests that augmented feedback may be effective. There is a need for a large pragmatic trial to explore the impact of augmented activity feedback on top of their standard care. The purpose of this study is to determine the effect of augmented activity feedback by smart watches to support in-patient stroke rehabilitation.
Detailed Description
This study had a feasibility and pilot development phase from September 2015 to April 2016, and then moved into the main study with some changes in design and execution occurring in the light of experience. Its execution has also been constrained by external factors beyond control. It is in essence asking whether wearing a Smart Watch which gives feedback on activity every two hours, with a specific target tailored to the patient's performance 24 hours earlier will be associated with a higher rate of physical activity than seen in people wearing the same watch without and feedback been given. The intervention only lasts unto 21 days, but earlier discharge will terminate that patient's participation sooner. A telephone interview at 12 weeks after entry collect data on mobility. Outcome measures will assess mobility, activity, and health status.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A randomised, parallel group, single-blinded, attention and feedback controlled study
Masking
InvestigatorOutcomes Assessor
Masking Description
The patients wear identical watches; one gives no feedback on activity levels and one gives feedback on a two-hourly basis, with progress against a target derived from activity 24 hours earlier.
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Feedback against tailored target
Arm Type
Experimental
Arm Description
For each two hour epoch, the watch calculate the level of activity for the same epoch the day before, and adds 5% as the new target to be achieved.
Arm Title
No Feedback
Arm Type
Sham Comparator
Arm Description
For participants assigned to the control group, the smart watch will not provide any activity feedback against a target; it simply shows which two hour epoch a person is in.
Intervention Type
Behavioral
Intervention Name(s)
Feedback against tailored target
Intervention Description
Participants will wear a smart watch every weekday for nine hours during in-patient rehabilitation to monitor activity levels while receiving their usual care. In the active group, the watch will summate activity movement in two hour epochs and the target for the day for that epoch is the activity in the same epoch 24 hours earlier, plus 5%. During an epoch the patient is shown progress towards the target at at the end of an epoch, they will see their final process towards target for that epoch.
Intervention Type
Behavioral
Intervention Name(s)
No feedback
Intervention Description
Participants will wear a smart watch every weekday for nine hours during in-patient rehabilitation to monitor activity levels while receiving their usual care. However the watch face will simply show which epoch a person is in. The watch will collect the activity in exactly the same way over the day.
Primary Outcome Measure Information:
Title
Change in activity counts as measured by a triaxial accelerometer from a smart watch from admission to 3 weeks or discharge from rehabilitation
Time Frame
Baseline, Three weeks or at discharge from in-patient rehabilitation if sooner
Secondary Outcome Measure Information:
Title
Activity goal attainment as measured and provided by the smart watch
Description
Participants in feedback group receive a preset activity goal based on their previous activity levels at baseline. The smart watch will then provide graduated encouragement by increasing their activity goal by about 5%. Every 10-15 minutes the screen lights up and participants can see their activity progress expressed by activity bars (representing 0-100%). Participants reaching their activity goal is used to measure goal attainment.
Time Frame
At three weeks, or discharge if sooner
Title
Change in walking mobility
Description
Change in walking speed and spatio-temporal characteristics of walking as measured by an inertial sensor on the lower trunk during a 10m walk test.
Time Frame
Baseline, Three weeks or discharge from in-patient rehabilitation if sooner
Title
Fatigue
Description
Fatigue Severity Index
Time Frame
Baseline, Three weeks or discharge from in-patient rehabilitation if sooner
Title
Health status on EQ-5D-5L
Description
This scale is used a measure for health status and compromises 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression
Time Frame
Baseline, Three weeks or discharge from in-patient rehabilitation if sooner, and 12 weeks (by telephone)
Title
Change in functional mobility as measured by Rivermead Mobility Index (RMI)
Description
This scale assesses functional mobility in gait, balance and transfers after stroke
Time Frame
Baseline, Three weeks or discharge from in-patient rehabilitation if sooner, and 12 weeks (by telephone)
Title
Change in cognitive function as measured by The Montreal Cognitive Assessment (MoCA)
Description
This is a screening instrument for to measure mild cognitive dysfunction. It assesses different cognitive domains: attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation.
Time Frame
Baseline, Three weeks or discharge from in-patient rehabilitation if sooner
Title
Change in arm function recovery
Description
Grip dynamometer
Time Frame
Baseline, Three weeks or discharge from in-patient rehabilitation if sooner
Title
Change in performance of activities of daily living as measured by Barthel ADL Index
Description
This scale is used to record what the participant undertakes in personal activities, to establish a degree of independence from any help, physical or verbal.
Time Frame
Baseline, Three weeks or discharge from in-patient rehabilitation if sooner
Title
Change in disability as measured by WHO Disability Assessment Scale (12 item version)
Description
This scale provides a global measure of disability covering 6 domains: cognition, mobility, self-care, getting along, life activities, and participation
Time Frame
Baseline, Three weeks or discharge from in-patient rehabilitation if sooner, and 12 weeks
Title
Adverse events
Description
Self-reported adverse events
Time Frame
At three weeks, or discharge if sooner and at 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Admission for acute/sub-acute in-patient neurorehabilitation of a first stroke at the 2nd affiliated hospital of Anhui University of Traditional Medicine and Acupuncture, Hefei, China. Time from onset of stroke to admission for rehabilitation <16 weeks. Ability to follow a two stage command; pick up an object, put object on table. Independent in mobility prior to admission. Subjects can use any type of assistive device and brace needed. Able to understand and repeat information related to the Informed Consent. Exclusion Criteria: Admission for second stroke. Subjects who are unable to provide consent due to a cognitive impairment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yun Dong, Dr
Phone
+86 551 6266 5048
Email
dongyun1003@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Zhidao Xia, Dr
Email
zhidao.xia@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Derick T Wade, MD
Organizational Affiliation
Oxford Brookes University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The 2nd Affiliated Hospital to Anhui University of Tranditional Chinese Medicine
City
Hefei
State/Province
Anhui
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yun Dong, Dr
Phone
+86 551 6266 5048
Email
dongyun1003@126.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
In the unlikely event that someone asks, it will probably be shared but so far (March 2017) there is no plan
Citations:
PubMed Identifier
30323946
Citation
Lawrie S, Dong Y, Steins D, Xia Z, Esser P, Sun S, Li F, Amor JD, James C, Izadi H, Cao Y, Wade D, Mayo N, Dawes H; Smart Watch Activity Feedback Trial Committee (SWAFT). Evaluation of a smartwatch-based intervention providing feedback of daily activity within a research-naive stroke ward: a pilot randomised controlled trial. Pilot Feasibility Stud. 2018 Oct 6;4:157. doi: 10.1186/s40814-018-0345-x. eCollection 2018.
Results Reference
derived
PubMed Identifier
29523170
Citation
Dong Y, Steins D, Sun S, Li F, Amor JD, James CJ, Xia Z, Dawes H, Izadi H, Cao Y, Wade DT; Smart watch activity feedback trial committee (SWAFT). Does feedback on daily activity level from a Smart watch during inpatient stroke rehabilitation increase physical activity levels? Study protocol for a randomized controlled trial. Trials. 2018 Mar 9;19(1):177. doi: 10.1186/s13063-018-2476-z.
Results Reference
derived

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The Effect of Activity Feedback Enabled by Smart Watches During In-patient Stroke Rehabilitation

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