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Trial registered on ANZCTR
Registration number
ACTRN12621000945820
Ethics application status
Approved
Date submitted
10/02/2021
Date registered
19/07/2021
Date last updated
19/07/2021
Date data sharing statement initially provided
19/07/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
A pilot randomised controlled trial: Joint Walkers, a Group of Rheumatology Outdoor Walkers
(GROW Study)
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Scientific title
A pilot randomised controlled trial, with embedded qualitative component of, Joint Walkers, a Group of outpatient Rheumatology Outdoor Walkers.
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Secondary ID [1]
303201
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None
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Universal Trial Number (UTN)
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Trial acronym
GROW Study: Group of Rheumatology Outdoor Walkers
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
musculoskeletal pain
322890
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Condition category
Condition code
Musculoskeletal
318248
318248
0
0
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Osteoarthritis
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Inflammatory and Immune System
318249
318249
0
0
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Autoimmune diseases
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Musculoskeletal
318250
318250
0
0
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Osteoporosis
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Inflammatory and Immune System
318251
318251
0
0
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Rheumatoid arthritis
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Inflammatory and Immune System
319667
319667
0
0
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Connective tissue diseases
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Inflammatory and Immune System
319668
319668
0
0
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Other inflammatory or immune system disorders
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Musculoskeletal
319669
319669
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
All patients will receive usual physiotherapy outpatient care.
While the experimental group will be enrolled into “Joint Walkers” an outdoor walking group, 1.25 hours twice a week with a physiotherapist for 3 months, some strength exercises (for example, upper and lower limb exercise with a TheraBand ) will be included.
Flat terrain, seated rests, at patients tolerance, with approximately up to 20 participants. Recording attendance and patient encouraged to self track distances (app/ manually).
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Intervention code [1]
319501
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Treatment: Other
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Intervention code [2]
320568
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Lifestyle
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Intervention code [3]
320569
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Behaviour
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Comparator / control treatment
All patients will receive usual physiotherapy outpatient care. In addition, the control group will be referred to "Get Healthy" NSW Government Program, for physical activity coaching, telephone coaching promoting healthy lifestyle including healthy eating, physical activity, weight management and alcohol reduction. Health coach, 10 confidential coaching phone calls, approximately 20min in length each , over six months, motivation and support to set healthy goals, information and journal to help track goals and overcome problems, option for re enrolment after 6 months, free NSW government service.
Control patients will be offered enrolment into Joint Walkers at the completion of the 3-month study duration, while those already attending will be supported to form a self-sustaining maintenance group. All patients will then be re-assessed at 6-months for all outcome measures
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Control group
Active
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Outcomes
Primary outcome [1]
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Composite primary outcome of feasibility
Assessed by: number participants recruited each month, proportion of eligible patients recruited per month, retention of participants in both arms of the study and adherence to completion of the intervention.
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Assessment method [1]
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Timepoint [1]
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3 & 6 months post commencement of the intervention
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Primary outcome [2]
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Primary clinical outcome: Change in walking activity, as measured using the subscale Walking Activity, using the Incidental and planned exercise questionnaire, version W .
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Assessment method [2]
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Timepoint [2]
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3 & 6 months from commencement of treatment
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Secondary outcome [1]
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Achievement of physical activity guidelines, as measured using the Incidental and planned exercise questionnaire, version W
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Assessment method [1]
390619
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Timepoint [1]
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3 & 6 months after commencement of the intervention
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Secondary outcome [2]
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Changes in self-efficacy with exercise, as measured using Self-Efficacy with Exercise Scale
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Assessment method [2]
390620
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Timepoint [2]
390620
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3 & 6 month after commencement of intervention
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Secondary outcome [3]
395608
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Experiences of Social Cohesion as measured using The Physical Activity Group Environment Questionnaire
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Assessment method [3]
395608
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Timepoint [3]
395608
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3 & 6 months after commencement of treatment
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Secondary outcome [4]
396852
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Participant feedback regarding the acceptability of the intervention via a 20 minute open ended phone interview
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Assessment method [4]
396852
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Timepoint [4]
396852
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3 months post start of intervention
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Eligibility
Key inclusion criteria
• Over the age of 18
• Consulted Rheumatology Physiotherapy service at Liverpool Hospital
• Independently mobile in the community
• Medically cleared to attend Joint Walkers
• Can communicate with staff in English or are able to bring a bilingual support person to their walking session (should they be allocated to this arm)
• Have the cognitive capacity to give informed consent
• Available twice a week to attend a walking group for 3 months
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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
• Unable to navigate the community independently
• Unable to safely communicate with staff or bring a bilingual support person.
• Unavailable to attend a walking group twice a week
• Condition medically unstable
• Condition with a prognosis of functionally deterioration over the next 3 months deeming patient unsafe to complete program
• Lack capacity to provide consent
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Study design
Purpose of the study
Treatment
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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)
sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
simple randomisation using randomisation table created by computer software
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people assessing the outcomes
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Intervention assignment
Other
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Other design features
Pilot randomised controlled trial with embedded Qualitative component
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Comparisons between two therapy groups and within therapy groups will be performed.
Sample size calculations have been based on achieving a large effect size (0.8) difference between the two groups in the primary outcome measure
Primary outcome being amount of walking as per the Incidental and planned exercise, “walking activity” subscale. A sample of 62 patients has been calculated as sufficient to detect , a large effect size of 0.8 a difference of 5.44 walking hours over the weekhours, between the two groups based on previous activity research.
groups assuming the Get Healthy group walk an average of 6.24hrs , SD 6.77hrs in both groups, 80% power , 5% significance with a lost to follow up at 15%, a total of 62 patients.
The Joint walker program feasibility concept will be assessed by documenting: number eligible, number enrolled, attendance rates, and adverse events and the number continuing a self-directed group beyond the 3-month supervised period.
Participants feedback regarding their additional therapy will be documented from interviews
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
6/09/2021
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Actual
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Date of last participant enrolment
Anticipated
2/05/2022
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Actual
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Date of last data collection
Anticipated
31/12/2022
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Actual
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Sample size
Target
62
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
18690
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Liverpool Hospital - Liverpool
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Recruitment postcode(s) [1]
33127
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2170 - Liverpool
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Funding & Sponsors
Funding source category [1]
307602
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Hospital
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Name [1]
307602
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In kind support from Liverpool Hospital
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Address [1]
307602
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Liverpool health services Locked Bag 7103 Liverpool BC NSW 1871
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Country [1]
307602
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Australia
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Primary sponsor type
Charities/Societies/Foundations
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Name
Liverpool Hospital
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Address
Liverpool health services Locked Bag 7103 Liverpool BC NSW 1871
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Country
Australia
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Secondary sponsor category [1]
308295
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None
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Name [1]
308295
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Address [1]
308295
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Country [1]
308295
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
307656
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South Western Sydney Local Health District Human Research Ethics Committee
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Ethics committee address [1]
307656
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1 Campbell Street Liverpool 2170 NSW
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Ethics committee country [1]
307656
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Australia
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Date submitted for ethics approval [1]
307656
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10/02/2021
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Approval date [1]
307656
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21/04/2021
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Ethics approval number [1]
307656
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2020/ETH02360
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Summary
Brief summary
Proof of concept. We would like to explore the feasibility of implementing a build a self-sustaining walking group of similar people from the rheumatology outpatient clinic with musculoskeletal conditions living with chronic disease who are motivated to improve their lifestyle. In addition, to increase the physical activity levels & self-efficacy with exercise for rheumatology physiotherapy outpatients. We hypothesise that Joint Walkers will increases in walking activity, and Achievement of Performance of physical activity guidelines. We also hope to increase the patients self-efficacy with exercise & engage with others of similar health conditions in a supportive environment
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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
108030
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Mrs Sacha Bossina
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Address
108030
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Liverpool Hospital, Physiotherapy Deaprtment, Level 2 Health Services Building ,Goulburn and Campbell St Liverpool NSW 2170
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Country
108030
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Australia
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Phone
108030
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+61 2 87384707
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Fax
108030
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Email
108030
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[email protected]
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Contact person for public queries
Name
108031
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Sacha Bossina
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Address
108031
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Liverpool Hospital, Physiotherapy Department, Level 2 Health Services Building ,Goulburn and Campbell St Liverpool NSW 2170
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Country
108031
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Australia
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Phone
108031
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+61 2 87384759
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Fax
108031
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Email
108031
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[email protected]
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Contact person for scientific queries
Name
108032
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Sacha Bossina
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Address
108032
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Liverpool Hospital, Physiotherapy Department, Level 2 Health Services Building ,Goulburn and Campbell St Liverpool NSW 2170
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Country
108032
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Australia
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Phone
108032
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+61 2 87384759
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Fax
108032
0
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Email
108032
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
deidentified outcome measures: individual participant data published results
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When will data be available (start and end dates)?
At the end of trial, once 62 participants recruited and results collated, potentially up until 2023
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Available to whom?
via publication
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Available for what types of analyses?
qualitative and quantitative analysis to reflect the aims of the study protocol
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How or where can data be obtained?
via publication
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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
No additional documents have been identified.
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