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The Mechatronic Remote Physiotherapy System (MRPS) in Remote Stroke Rehabilitation

NCT06964789 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2025-05-14

No results posted yet for this study

Summary

The aim of this pilot trial is to examine and compare the safety and feasibility of enhanced Early Supported Discharge (ESD) through the Mechatronic Remote Physiotherapy System (MRPS) and traditional ESD after stroke.

The main questions this trial aims to answer are:

* Is enhanced ESD via the MRPS safe, feasible and significantly different compared to traditional ESD when administered to patients after stroke?
* Do patients interact with and are they satisfied with the MRPS?
* Is enhanced ESD cost-effective compared to traditional ESD?
* Are there any adverse effects of the MRPS and what are the areas for further improvement?

Participants in the experimental group will receive enhanced ESD through the MRPS.

The intervention will be given for approximately 6-8 weeks in total. Frequency will be determined by how often the participants' use the MRPS themselves. Frequency of use and level of completion of each session will be monitored. Enhanced ESD therapy sessions will be designed to reflect traditional ESD sessions.

Participants in the control group will receive traditional ESD. The intervention will be given for approximately 6-8 weeks in total with a frequency of 1-3 therapy visits per week (as per traditional ESD). Therapy sessions will be designed by therapists delivering the ESD service.

Conditions

  • Stroke
  • Neurological Disorder

Interventions

DEVICE

Mechatronic Remote Physiotherapy System (MRPS)

The MRPS is an Online Rehabilitation Platform for neurology patients. The platform has been designed to provide supervised and monitored remote rehabilitation therapy, initially focusing on patients who have suffered a stroke. The system comprises of a patent pending mirror therapy strengthening device, which is a neural therapy device using mirror therapy and exercise apparatus for upper limb rehabilitation. The platform also permits the addition of modules beneficial to the patients' recovery. A sensory substitution balance apparatus and motion detecting sensors are also being designed to connect to the system to allow for lower limb rehabilitation.

OTHER

Early Supported Discharge

ESD is a multidisciplinary service providing medically stable patients continued therapy and healthcare in the community.

Sponsors & Collaborators

  • Sligo General Hospital

    collaborator OTHER

  • Institute of Technology, Sligo

    lead OTHER

Principal Investigators

  • Kenneth Monaghan, PhD · ATU Sligo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-01
Primary Completion
2026-09-01
Completion
2027-12-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06964789 on ClinicalTrials.gov