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A mobility booster program (HiWalk) in long-term community stroke rehabilitation

Preliminary investigation of the effect of a mobility booster program (HiWalk) on walking speed in long-term community stroke rehabilitation

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623000316606
Enrollment
47
Registered
2023-03-23
Start date
2023-06-28
Completion date
2024-01-10
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This project will investigate a new, short-term mobility program known as the HiWalk program. HiWalk is a physiotherapy program provided at a time of need - meaning if the stroke survivor is experiencing challenges with their mobility or has a new mobility goal (even years after stroke), then this three-week program may assist their walking ability. Our preliminary research has demonstrated that HiWalk could be successfully implemented in the community after stroke and that the HiWalk program was enjoyed by people after stroke. The next, phase of research for the HiWalk program is a pilot trial of HiWalk allowing us to test the program in a clinical trial setting.

Interventions

Participants will receive the HiWalk program for 3 weeks (up to 3 hours a day, five days a week, totaling 45 hours). The HiWalk program consists of an individually tailored motor training program (strength, balance and task training) and specific mobility practice. Some more specific examples include, within strength training participants will complete strengthening exercises of the lower limbs. For mobility practice walking overground or on a treadmill will be practiced, including negotiating o

Participants will receive the HiWalk program for 3 weeks (up to 3 hours a day, five days a week, totaling 45 hours). The HiWalk program consists of an individually tailored motor training program (strength, balance and task training) and specific mobility practice. Some more specific examples include, within strength training participants will complete strengthening exercises of the lower limbs. For mobility practice walking overground or on a treadmill will be practiced, including negotiating obstacles. Embedded throughout the program is a self-management approach. Participants are guided through the Taking Charge program and set individualised mobility goals. Taking charge is a workbook that asks the individual to reflect on their strengths and challenges and identify the next steps in their recovery journey. A standardised program assessment identifies the individual program for each participant. The exercise component is delivered as a small group (4-5 participants, 1 facilitator). Each participant's program is reviewed weekly to ensure it remains suitable and is progressed in difficulty as appropriate. If outside of the HiWalk weeks participants usually access therapy they will continue to participate in their usual therapy program which may or may not include physiotherapy. The HiWalk program is led by a physiotherapist and sessions are facilitated by a physiotherapist, exercise physiologist or allied health assistant/student. Sessions are completed face-to-face in a community rehabilitation gym. Most sessions are completed as a small group (4-5 people). The program assessment and weekly review are completed one-to-one between each participant and a program therapist. Each activity within the program has individualised plans developed with the therapist and the participant. Each activity has pre-planned levels of difficulty and modifications that may be enacted in order to individualise the activity to the participants ability. Adherence to the intervention will be recorded as session attendance (proportion of program sessions attended) and session participation (time attended and exercise repetitions completed).

Sponsors

Macquarie University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. An adult with a diagnosis of stroke > 6 months and < 8 years prior to study commencement 2. Able to walk without assistance of a person or aid over 10 m at a speed of 0.4-1.0 m/s 3. Willing to participate in the high dose therapy program (five days a week) at a local trial site

Exclusion criteria

Unable to follow two step instructions

Outcome results

None listed

Source: ANZCTR · Data processed: Aug 31, 2026