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Repetitive Exercise for People after Stroke (REPS): a pilot randomised controlled trial

Repetitive Exercise for People after Stroke (REPS): effects on functional performance.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616001288415
Enrollment
26
Registered
2016-09-13
Start date
2016-09-22
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Following acquired brain injury (ABI) caused by stroke or trauma many people cannot move around independently due to motor impairments such as weakness and poor coordination. These people require intensive repetitive practice to improve their ability to move around. Therefore the aim of this study is to determine if a two-week intensive package of functional training improves functional performance more than usual care in people with ABI admitted to a sub-acute ward for rehabilitation. Experimental design: An assessor blinded randomised controlled trial will be conducted. Each participant will be randomly allocated to an experimental or control group using the principles of concealed allocation. Participants allocated to the experimental group will receive usual care and a 2-week package of exercises and strategies that will provide them with additional opportunities to practice a functional task. This package will include a range of strategies individualised to the needs of the participant for increasing the amount of practice of a functional task. Participants allocated to the control group will receive usual care. Usual care for both groups will consist of two one-hour sessions of physiotherapy a day and will include one-to-one or group therapy with a physiotherapist. This therapy will involve strength, endurance, balance and coordination exercises as well as task-specific practice of sitting, sitting-to-standing, standing, and walking. All exercises will be tailored to the needs of each participant. Participants: 30 consecutively admitted patients to a sub-acute general adult rehabilitation unit.

Interventions

Participants allocated to the experimental group will receive usual care (see Usual care) and a 2-week package of exercises and strategies that will provide them with additional opportunities to practice a functional task*. This package will include a range of strategies* individualised to the needs of the participant for increasing the amount of practice of a functional task. Participants will be required to perform as many repetitions of this task as they can per day. *Details of functiona

Participants allocated to the experimental group will receive usual care (see Usual care) and a 2-week package of exercises and strategies that will provide them with additional opportunities to practice a functional task*. This package will include a range of strategies* individualised to the needs of the participant for increasing the amount of practice of a functional task. Participants will be required to perform as many repetitions of this task as they can per day. *Details of functional tasks and strategies used to increase repetitive practice have been omitted to minimise contamination between groups.

Sponsors

Davide de Sousa
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

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

Inclusion criteria

Diagnosis of a first time stroke or any other acquired brain injury (ABI) that is not progressive Acute event < 6 months before the study onset Sufficient communication skills to indicate yes/no verbally or via gestures Sufficient cognition to consent or consent will be obtained from the person responsible Stroke/ABI has affected the ability to STS

Exclusion criteria

Limited joint range of movement or musculoskeletal conditions that would prevent participation Inability to participate in exercise i.e. Medically unwell Unable to follow instructions Expected length of stay of < 2 weeks

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026