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FREEHAB clinical evaluation of a prototype physiotherapy device

FREEHAB within session evaluations of a prototype device for improving patients’ sit to stand movements

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12643856
Enrollment
24
Registered
2023-06-14
Start date
2024-02-12
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Stroke or acquired brain injury Injury, Occupational Diseases, Poisoning

Interventions

This is a small non-randomised clinical investigation of sitting-to-standing performance in a controlled laboratory setting, followed by a questionnaire about the acceptability of an assistive robotic

Sponsors

University of Bristol
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosis of stroke or acquired brain injury with hemiparesis (weakness on one side of the body) 2. Received or are receiving treatment from a physiotherapist in the clinical partner service for rehabilitation of mobility including sitting to standing (STS) in the previous 6 months 3. Able to STS without help from another person (e.g. physiotherapist), but may need to use a high seat and be slow to stand up 4. Medically stable 5. Mental capacity to consent to the study according to members of the clinical team who are working with the patient

Exclusion criteria

Exclusion criteria: 1. Patients with concurrent acute musculoskeletal conditions (e.g., Fractures, sprains) which prevent weight bearing 2. Patients with skin or soft tissue damage or pressure ulcers that would impact the application of the device 3. Patients with a percutaneous endoscopic gastrostomy (PEG) feeding tube 4. Patients regularly experiencing drowsiness or dizziness 5. Patients with a diagnosis of any neurological disorder other than stroke or traumatic brain injury 6. Patients with balance problems, e.g., orthostatic hypotension, vertigo 7. Patients with a body weight in excess of 90Kg

Design outcomes

Primary

MeasureTime frame
The centre of mass vertical velocity measured using a Qualysis camera-based movement analysis system and Inertial Measurement Units (IMUs) while performing the movement of sit to stand (repeated three times, for each block)

Secondary

MeasureTime frame
Knee joint velocity and weight-bearing asymmetry measured using a Qualysis camera-based movement analysis system and Inertial Measurement Units (IMUs) while performing the movement of sit to stand (repeated three times, for each block)

Countries

England, United Kingdom

Contacts

Public ContactLeah Morris
leah.morris@uwe.ac.uk+44 (0)117 3286908

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026