Use of Virtual Reality Game in Rehabilitation of Stroke Patients in Tan Tock Seng Hospital

NCT ID: NCT04874181

Last Updated: 2021-05-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-07-27

Study Completion Date

2021-04-13

Brief Summary

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Use of SIlverfit 3d to aid in rehab of stroke patients focusing on their shoulder and knee strength

Detailed Description

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Either 1 of 3 physiotherapists will recruit the patient from NICU if the GCS is 14 - 15. Silverfit 3D will then be used for 20 minutes each day to train the knee and arm strength until the patient's discharge from ICU. Baseline muscle strength will be measured and graded by the physiotherapist using Medical Research Council grading then followed up by the same physiotherapist on discharge from ICU and on discharge from hospital.

Conditions

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Stroke, Acute

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Single Arm study
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Silverfit 3D

The subject will use SIlverfit 3D for rehabilitation of his/her shoulder/knee strength post stroke.

Group Type EXPERIMENTAL

Silverfit 3D

Intervention Type DEVICE

Virtual reality game used for rehabilitation of stroke patients

Interventions

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Silverfit 3D

Virtual reality game used for rehabilitation of stroke patients

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients 21 - 90 years old
* Diagnosis of stroke of pure motor/sensory type affecting the limbs, all levels of severity and at all stages post stroke, defined by the WHO as "a syndrome of rapidly developing symptoms and signs of focal, and at times global, loss of cerebral function lasting more than 24 hours or leading to death with no apparent cause other than that of vascular origin" (WHO 1989), diagnosed by imaging or neurological examination
* GCS 14 - 15
* RASS -1 to +1
* Blood pressure within 20% of patient's baseline
* Muscle power at least 2 out of 5 on the affected side, as assessed by the physiotherapist or clinician

Exclusion Criteria

* Age less than 21 or more than 90 years old
* Neurological instability
* Poor prognosis/expected withdrawal of treatment/palliative care patient
* Visual loss/hearing loss
* Active delirium with inability to cooperate as determined by CAM-ICU positivity
* Severe cognitive impairment/dementia
* Haemodynamic instability
Minimum Eligible Age

21 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tan Tock Seng Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Tan Tock Seng Hospital

Singapore, , Singapore

Site Status

Countries

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Singapore

Other Identifiers

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2020/00143

Identifier Type: -

Identifier Source: org_study_id

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