New Technologies in the Rehabilitation of Chronic Stroke (SRTI)

Markus Wirz

Status: Completed

Conditions: Stroke; Hemiplegia

Treatments: Other: Rehabilitation technology

Study type: Interventional

Funder types: Other

Identifiers

NCT03641651

ZHAW-SRTI

Details and patient eligibility

About

The objective of the current study is to develop and investigate training concepts involving rehabilitation technology, which aim at exploiting the potential for regaining the ability to perform skilled movements by maximizing training intensity and keeping the motivation of patients high.

The evaluation focuses on feasibility and cost-benefit analyses

Full description

This feasibility project aims to establish an efficient setting for intensive rehabilitation with new technology in four trailblazer clinics. This will enable them to provide intensive therapy to the patients in accordance with the study protocol. If this setting is integrated into the clinical routine, the investigators will be able to collect data to get some first insight into economic and functional data required to calculate changes in socioeconomic costs

Enrollment: 15 patients

Sex: All

Ages: 18 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patients with residual hemiparesis after cerebrovascular accident
• Up to 12 months after the event
• Primary rehabilitation terminated
• Able to cognitively comprehend the aim of the project with at least 22 points in the Montreal Cognitive Assessment (MoCA)
• General health condition allows for intensive rehabilitative training with limited supervision i.e. clearance and prescription of responsible physician
• Understand written and spoken German language

Exclusion criteria

Patients with any signs and symptoms showing that the participant is unwilling to participate in the study will result in the patient being excluded from participation Any medical condition preventing participation such as Severe respiratory disease Severe OR unstable cardio-circulatory conditions Orthopaedic conditions, especially in extremities targeted for rehabilitation such as

• fixed joint contractures limiting range of motion
• non-consolidated fractures Neuro-psychological conditions including cognitive deficits limiting communication or non-cooperation like (self-) aggressive behaviour Infections or inflammatory diseases, like osteomyelitis

Specific absolute contraindication for the training with any of the respective devices:

• Improper fit of the device, including its harness to relevant extremity(ies)
• Contraindicated training position (standing, sitting)

Device specific contraindications will be respected and will lead to the exclusion of the device for that patient.

Trial design

Primary purpose: Health Services Research

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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15 participants in 1 patient group

Technology arm

Experimental group

Description:

4 Weeks intervention of intensive rehabilitation using rehabilitation technology, 3-5 h per day, within a 5d week in-or outpatient setting.

Treatment:

Other: Rehabilitation technology