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Network of sites and ‘up-skilled’ therapists to deliver best-practice stroke rehabilitation of the upper limb.

Network of sites and ‘up-skilled’ therapists to deliver best-practice stroke rehabilitation of the upper limb.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001389291
Acronym
SENSe CONNECT
Enrollment
208
Registered
2018-08-20
Start date
2018-09-14
Completion date
2021-09-17
Last updated
2018-09-17

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 study will involve the creation of a Knowledge Translation Hub and a network of specialist therapy centres in Australia. The translational hub will inform and guide stakeholders in knowledge translation, upskill therapists and establish a community of practice. The specialist therapy centres will deliver SENSe to people with stroke, and provide training to upskill therapists. The study will monitor a range of outcomes including touch sensation, functional use of the hand, and return to personally-important activities for survivors of stroke, therapist confidence to deliver SENSe, and costs to implement the service. The project has been funded by the NHMRC as a partnership grant to implement evidence into practice.

Interventions

Two participant groups are provided with interventions: 1. People with stroke and somatosensory loss 2. Therapists (occupational therapists and physiotherapists) Participant Group 1 (People with stroke) – will receive SENSe Therapy. SENSe Therapy (as outlined in the Study of the Effectiveness of Neuro-rehabilitation on Sensation, by Carey et al., 2011), is a science and evidence based rehabilitation therapy to improve the sense of touch when touching objects and using the hand in everyday

Two participant groups are provided with interventions: 1. People with stroke and somatosensory loss 2. Therapists (occupational therapists and physiotherapists) Participant Group 1 (People with stroke) – will receive SENSe Therapy. SENSe Therapy (as outlined in the Study of the Effectiveness of Neuro-rehabilitation on Sensation, by Carey et al., 2011), is a science and evidence based rehabilitation therapy to improve the sense of touch when touching objects and using the hand in everyday tasks. The intervention will be delivered face to face by Occupational Therapists and/or Physiotherapists within specialist therapy centres. The intervention involves sensory discrimination training of texture discrimination, sensing the position of the upper limb in space, recognising objects through the sense of touch and learning how to apply these skills in daily tasks identified by the person with stroke. The intervention will be tailored according to level of impairment and functional goals. The dose will be 10 one-hour sessions, over a period of 6 weeks. The frequency of sessions will be 1 to 2 times a week. Fidelity of the intervention will be assessed using checklists (with self-evaluation and evaluation via an independent blinded SENSe Trainer) and audit of treatment notes. Carey, L.M., R. Macdonnell, and T. Matyas, SENSe: Study of the Effectiveness of Neurorehabilitation on Sensation. A randomized controlled trial. Neurorehabilitation and Neural Repair, 2011. 25: p. 304-313. Participant Group 2 (Therapists) – will be involved in an implementation intervention to change behaviour. Occupational therapists and physiotherapists will be involved in an implementation intervention and receive training to deliver SENSe Therapy. Therapists will be up-skilled in delivery of SENSe Therapy using interactive workshops facilitated by trained clinical researchers and involving multimedia resources. The workshops will involve 3 x 4 hours sessions, and be supported by independent learning modules (estimated to take 1 to 2 hours each). The participants who are therapists will also receive supervision and mentoring so they can deliver SENSe Therapy to people with stroke within specialist therapy centres. The knowledge and skill of therapists will be measured before, during and after delivery of SENSe Therapy and during the up-skilling process. Confidence and ability to deliver SENSe Therapy will be evaluated, and will include assessment of treatment fidelity. Treatment fidelity will include self-evaluation and assessment by blinded SENSe Therapy Trainers. This process will use criterion checklists to rate fidelity of the intervention observed via video recordings, and documented in the treatment notes.

Sponsors

Professor Leeanne Carey
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Key inclusion criteria are listed for the two groups of participants. Participants with stroke. * A clinical diagnosis of stroke: This can include infarct, haemorrhage, brainstem events, infarct following subarrachoid haemorrhage, and can include people with a second stroke. There will be no restriction on time since stroke. * Impaired touch sensation, limb position sense, and/or tactile object recognition of the upper limb, identified clinically and by standardized tests. *Medically stable * Able to give informed consent (with the use of an interpreter if English language proficiency is not sufficient to communicate study information adequately). * Comprehend simple instructions (follow 3 stage instructions and sustain attention for treatment) * Willing to commit time to participate in the SENSe Therapy program *Living in the community. Participants who are Therapists: * Occupational Therapist or Physiotherapist * Registered to practice. * Willing to participate in the training, undertake evaluation and actively participate in mentoring in order to develop competency to deliver SENSe Therapy.

Exclusion criteria

For participants with stroke. * Not medically stable * Sensory impairment is not due to stroke (eg carpal tunnel syndrome) * Severe unilateral spatial neglect * Prior history of other central nervous system dysfunction with unstable or progressive prognosis. * Severe peripheral neuropathy in the upper limb * Severe to moderate cognitive impairment * Not able to comprehend simple instructions or sustain attention needed to participate in treatment * Not able to give informed consent * Physical limitations that prevent participate in therapy tasks (e.g., contracture of the hand, or unhealed wounds.) * Unable to participate in a clinical appointment lasting 30 minutes There are no additional exclusion criteria for the participants who are therapists.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026