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Trial registered on ANZCTR
Registration number
ACTRN12616000230459
Ethics application status
Approved
Date submitted
11/02/2016
Date registered
19/02/2016
Date last updated
1/03/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
The effectiveness of a stretching intervention in lowering plantar pressures related to reduced ankle range of motion in people with diabetes.
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Scientific title
The effectiveness of a stretching intervention in lowering plantar pressures related to reduced ankle range of motion in people with diabetes.
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Secondary ID [1]
288495
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none
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Universal Trial Number (UTN)
U1111-1179-3343
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Diabetes
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Foot plantar pressure
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Condition category
Condition code
Physical Medicine / Rehabilitation
297757
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0
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Other physical medicine / rehabilitation
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Metabolic and Endocrine
297826
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0
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
8 week home based stretching program.
The stretching program will consist of a standing static lunge calf stretch, which will be held for 30 seconds and repeated 4 times on each leg during each session. Participants will be required to perform one stretching session per day, five days a week, for the eight week trial period.
Participants will complete a daily stretch diary to record how often they did the stretches.
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Intervention code [1]
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Prevention
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Intervention code [2]
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Treatment: Other
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Comparator / control treatment
The control group will undertake their usual activities for the intervention period
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Control group
Active
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Outcomes
Primary outcome [1]
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Peak pressure under defined areas of the foot (e.g. forefoot, midfoot, heel) measured in-shoe using the pedar-x system with flexible insoles, and measured barefoot using the Tekscan HR mat pressure platform.
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Assessment method [1]
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Timepoint [1]
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8 weeks and 16 weeks following baseline
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Primary outcome [2]
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Ankle dorsiflexion range of motion measured in:
- weightbearing using a weight-bearing lunge position, with knee extended and a digital inclinometer,
- non weightbearing using a modified Lidcombe template, with a force gauge and a digital inclinometer, which allows a standardised magnitude and direction of force to be applied to the ankle.
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Assessment method [2]
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Timepoint [2]
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8 weeks and 16 weeks following baseline
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Secondary outcome [1]
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Pressure-time integrals under defined areas of the foot (e.g. forefoot, midfoot, heel, etc) measured in-shoe using the pedar-x system with flexible insoles, and measured barefoot using the Tekscan HR mat pressure platform.
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Assessment method [1]
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Timepoint [1]
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8 weeks and 16 weeks following baseline
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Secondary outcome [2]
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Peak force under defined areas of the foot (e.g. forefoot, midfoot, heel, etc) measured in-shoe using the pedar-x system with flexible insoles, and measured barefoot using the Tekscan HR mat pressure platform.
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Assessment method [2]
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Timepoint [2]
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8 weeks and 16 weeks following baseline
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Secondary outcome [3]
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Contact area under defined areas of the foot (e.g. forefoot, midfoot, heel, etc) measured in-shoe using the pedar-x system with flexible insoles, and measured barefoot using the Tekscan HR mat pressure platform.
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Assessment method [3]
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Timepoint [3]
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8 weeks and 16 weeks following baseline
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Secondary outcome [4]
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Contact time under defined areas of the foot (e.g. forefoot, midfoot, heel, etc) measured in-shoe using the pedar-x system with flexible insoles, and measured barefoot using the Tekscan HR mat pressure platform.
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Assessment method [4]
320626
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Timepoint [4]
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8 weeks and 16 weeks following baseline
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Secondary outcome [5]
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Physical activity as measured by International Physical Activity Questionnaire Short Form (IPAQ-SF)
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Assessment method [5]
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Timepoint [5]
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8 weeks and 16 weeks following baseline
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Eligibility
Key inclusion criteria
a) reduced ankle dorsiflexion range of motion (equinus) defined as ankle dorsiflexion range of motion of less than or equal to five degrees
b) males and females 18 years of age and over
c) with a diagnosis of diabetes confirmed by medical records
d) able to speak and read basic English
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
a) current foot ulcer
b) any amputation in the lower limb
c) any self-reported neurological condition (other than loss of sensation due to diabetes) that
may affect the lower limb such as multiple sclerosis, stroke or polio
d) surgery to the foot or lower limb involving fixation of a joint
e) any condition precluding the participant from taking part in the foot pressure assessment
or ankle stretching program, such as not being able to walk 8m unaided
f) pregnancy
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
By selection of sequentially numbered, opaque sealed envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a computer generated random allocation schedule
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
To determine the effect of an eight week calf stretching program on the primary outcome of ankle dorsiflexion range of motion, and to allow statistical analysis to determine participant factors correlated with an increase in ankle dorsiflexion, a minimum sample size of 34 per group will be required for the randomised controlled trial.
The calculations are based on the following assumptions:
1) an SD of 6.5 degrees and difference of 5 degrees between the control group and the experimental group being clinically meaningful;
2) a power of 0.80 and alpha of 0.05 and;
3) a 20% attrition rate.
All data will be explored for normality prior to inferential analysis. One-way analysis of variance (ANOVA) with Bonferroni-adjusted post-hoc tests will be used to compare pressure measurements under various sites of the foot between the two test groups before and after the stretching program.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
6/09/2016
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Actual
16/09/2016
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Date of last participant enrolment
Anticipated
30/04/2018
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Actual
15/10/2017
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Date of last data collection
Anticipated
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Actual
19/12/2017
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Sample size
Target
68
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Accrual to date
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Final
68
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Recruitment in Australia
Recruitment state(s)
NSW
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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University of Newcastle
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Address [1]
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School of Health Sciences
PO Box 127
Ourimbah, NSW 2258
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Country [1]
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Australia
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Primary sponsor type
University
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Name
University of Newcastle
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Address
School of Health Sciences
PO Box 127
Ourimbah, NSW 2258
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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The University of Newcastle Human Research Ethics Committee
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Ethics committee address [1]
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The Chancellery University of Newcastle Callaghan Campus University Drive Callaghan NSW 2308
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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18/09/2015
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Approval date [1]
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21/12/2015
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Ethics approval number [1]
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H-2015-0354
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Summary
Brief summary
Diabetes is one of the most common chronic diseases in the world, affecting over 8% of the global population and is associated with a life-time risk of foot ulcers of 12-25%. Foot ulcers lead to high morbidity, increased associated healthcare costs and are the most important risk factor for lower extremity amputation. Elevated forefoot plantar pressure is a risk factor for foot ulceration and has been linked to reduced ankle dorsiflexion range of motion (equinus) in people with diabetes. Calf muscle stretching has been demonstrated to improve ankle joint range of motion across both the young and older adult healthy populations, and a pilot trial has demonstrated a reduction in plantar pressures following range of motion exercises in people with diabetes. Calf muscle stretching may be a simple, non-invasive and inexpensive method of increasing ankle joint range of motion resulting in decreased plantar pressures and a reduced risk of plantar ulceration in people with diabetes. The aims of this trial are 1) To determine if an 8 week calf stretching intervention will be effective in increasing ankle joint range of motion in people with diabetes and ankle equinus. 2) To determine if an increased ankle joint range of motion in people with diabetes and ankle equinus results in an associated reduction in forefoot plantar pressures.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Vivienne H Chuter
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Address
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University of Newcastle
School of Health Sciences
PO Box 127
Ourimbah, NSW 2258
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Country
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Australia
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Phone
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+ 61 2 4349 4424
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Vivienne H Chuter
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Address
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University of Newcastle
School of Health Sciences
PO Box 127
Ourimbah, NSW 2258
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Country
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Australia
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Phone
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+ 61 2 4349 4424
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Vivienne H Chuter
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Address
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University of Newcastle
School of Health Sciences
PO Box 127
Ourimbah, NSW 2258
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Country
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Australia
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Phone
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+ 61 2 4349 4424
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Calf muscle stretching is ineffective in increasing ankle range of motion or reducing plantar pressures in people with diabetes and ankle equinus: A randomised controlled trial.
2019
https://dx.doi.org/10.1016/j.clinbiomech.2019.07.005
N.B. These documents automatically identified may not have been verified by the study sponsor.
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