Effect of Nike FuelBand on Exercise and Function in Claudicants; a Randomised Controlled Trial
Primary Purpose
Peripheral Vascular Disease, Intermittent Claudication
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Nike FuelBand (NFB)
Sponsored by
About this trial
This is an interventional supportive care trial for Peripheral Vascular Disease focused on measuring Peripheral vascular disease
Eligibility Criteria
Inclusion Criteria:
- Age 40-80
- Referred to vascular rehabilitation service at St Marys Hospital (UK)
- IC involving the calf muscles
- Clinical and duplex investigations indicate Superficial Femoral Artery stenosis or occlusion
Exclusion Criteria:
- Clinical and duplex investigations indicate iliac disease
- Major joint disease in lower limb or lumbar spine/entrapment syndrome
- Significant cardiopulmonary limitations (NYHA>1)
- Maximum walking distance >500m
- Hospital inpatient/ living in a care home
- *Unfamiliarity with required technology
- History of dementia
- Unable to mobilize independently (does not include walking aids)
- IC not limiting factor of mobilization, limited by other medical problems
- Unable to attend supervised exercise programme
- Patient owns or uses any type of activity monitor
- Uses a walking frame *Patients should be able to use the NFB technology with minimal assistance
Sites / Locations
- Imperial College NHS Healthcare Trust- St Marys
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Nike FuelBand (NFB)
control
Arm Description
Patients will receive a Nike Fuel Band to encourage exercise.
Standard follow-up
Outcomes
Primary Outcome Measures
Maximum Walking Distances
Standardised treadmill test at the end of the study period
Secondary Outcome Measures
Pain Free Treadmill Walking Distance
Standardised treadmill test - first recognition of pain as reported by the patient.
Disease Specific Quality of Life
Assessed using VascuQol (Vascular Quality of life) Questionnaire score, range from 0 to 24, and higher value indicates a better health status.
Each question has a four-point response scale (1 most problems - 4 no problems)
Mood
Assessed using the Hospital Anxiety and Depression Scale score, participants reply that is closest to how they have been feeling in the past months. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 and 21 for either anxiety or depression. Score 0 to 3, 3 - Most of the time, 0 - Not at all.
Full Information
NCT ID
NCT01822457
First Posted
February 19, 2013
Last Updated
February 13, 2020
Sponsor
Imperial College London
1. Study Identification
Unique Protocol Identification Number
NCT01822457
Brief Title
Effect of Nike FuelBand on Exercise and Function in Claudicants; a Randomised Controlled Trial
Official Title
Effect of Nike FuelBand on Exercise and Function in Claudicants; a Randomised Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
August 2013 (Actual)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
August 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a randomised controlled study of patients suffering from intermittent claudication (IC), to assess the impact of wearing a Nike FuelBand (NFB) on walking distances, exercise levels and quality of life.
Detailed Description
IC manifests as pain in the calf, thigh or buttock muscles when walking. It is caused by narrowing or blockage of the blood vessels in the legs.
The NFB is a discrete wristband with a built-in accelerometer to measure motion. It provides estimates of the number of steps taken and the amount of distance covered each day.
This study will be conducted over a period of 18 months at Imperial College Trust's vascular outpatients service. Patients that meet the inclusion/exclusion criteria will be asked to consider participating. Participants will receive routine diagnostic work up with the addition of having their walking distances measured on a lab treadmill. They will also have their functional status and mood assessed using a questionnaire. These assessments will be carried out a total of five times over the course of the study. Patients will not need to make any additional visits to hospital.
Patients will be randomly allocated to either the NFB group or the control group. Patients in the NFB group will be given a FuelBand with instructions on how to use it. All patients will be given routine instructions on maintaining activity and target daily walking distances. Target walking distances will be programmed into the NFB. Patients in the NFB group will be asked to record estimates of how far they have walked each day directly from their band. All patients will be contacted by telephone at a pre-arranged time to collect recordings.
Patients will be followed up at their routine 3-month follow up appointment and additionally at 6 and 12 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Vascular Disease, Intermittent Claudication
Keywords
Peripheral vascular disease
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
37 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Nike FuelBand (NFB)
Arm Type
Experimental
Arm Description
Patients will receive a Nike Fuel Band to encourage exercise.
Arm Title
control
Arm Type
No Intervention
Arm Description
Standard follow-up
Intervention Type
Device
Intervention Name(s)
Nike FuelBand (NFB)
Intervention Description
The Nike Fuel Band (NFB) is a wrist-worn sensor with a built-in accelerometer for motion quantification. It is programmed to estimate the number of steps taken per day, and also predict energy expenditure in units known as Nike Fuel. Accompanying software allows the user to set daily targets and monitor their activity through a graphical user interface.
Primary Outcome Measure Information:
Title
Maximum Walking Distances
Description
Standardised treadmill test at the end of the study period
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Pain Free Treadmill Walking Distance
Description
Standardised treadmill test - first recognition of pain as reported by the patient.
Time Frame
12 months
Title
Disease Specific Quality of Life
Description
Assessed using VascuQol (Vascular Quality of life) Questionnaire score, range from 0 to 24, and higher value indicates a better health status.
Each question has a four-point response scale (1 most problems - 4 no problems)
Time Frame
12 months
Title
Mood
Description
Assessed using the Hospital Anxiety and Depression Scale score, participants reply that is closest to how they have been feeling in the past months. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 and 21 for either anxiety or depression. Score 0 to 3, 3 - Most of the time, 0 - Not at all.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 40-80
Referred to vascular rehabilitation service at St Marys Hospital (UK)
IC involving the calf muscles
Clinical and duplex investigations indicate Superficial Femoral Artery stenosis or occlusion
Exclusion Criteria:
Clinical and duplex investigations indicate iliac disease
Major joint disease in lower limb or lumbar spine/entrapment syndrome
Significant cardiopulmonary limitations (NYHA>1)
Maximum walking distance >500m
Hospital inpatient/ living in a care home
*Unfamiliarity with required technology
History of dementia
Unable to mobilize independently (does not include walking aids)
IC not limiting factor of mobilization, limited by other medical problems
Unable to attend supervised exercise programme
Patient owns or uses any type of activity monitor
Uses a walking frame *Patients should be able to use the NFB technology with minimal assistance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ara Darzi, MD, FRCS, FRS
Organizational Affiliation
Imperial College NHS Healthcare Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nicholas J Cheshire, MD, FRCS
Organizational Affiliation
Imperial College NHS Healthcare Trust
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Colin D Bicknell, MD, FRCS
Organizational Affiliation
Imperial College NHS Healthcare Trust
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Celia Riga, MD, FRCS
Organizational Affiliation
Imperial College NHS Healthcare Trust
Official's Role
Study Director
Facility Information:
Facility Name
Imperial College NHS Healthcare Trust- St Marys
City
London
ZIP/Postal Code
W21NY
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effect of Nike FuelBand on Exercise and Function in Claudicants; a Randomised Controlled Trial
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