Study Results
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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COMPLETED
NA
6 participants
INTERVENTIONAL
2021-01-13
2023-10-31
Brief Summary
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Detailed Description
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As people become increasingly immobile, they become restricted in their ability to perform activities of daily living, access the outdoors, participate in preferred occupational roles or engage in leisure activities. Consequently, there is a deterioration in their ability to experience well being and have quality of life. There is also a significant carer burden as the carer spends long hours in the day looking after the person. The average disease trajectory lasts between 3-5 years, followed by death. More recently, the use of Virtual Reality (VR) technology is being recognised in the field of health. This technology uses the interactions between an individual and a computer generated environment to stimulate different sensory modalities such as visual and auditory. The technology can be accessed commonly using head mounted goggles or head sets. The entertaining or stimulating effect of VR is useful in redirecting the person's attention away from the distressing experiences, such as pain and anxiety. The purpose of this study is to establish if VR is useful for people with MND and if it helps improve their well being.
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Intervention
The intervention period will last 4 weeks where participants will be required to use the VR set and document the time of use in a daily diary
Virtual Reality Headset
Virtual Reality Headset
Interventions
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Virtual Reality Headset
Virtual Reality Headset
Eligibility Criteria
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Inclusion Criteria
2. Sufficient cognitive ability to understand instructions with regards using the VR kit (ECAS score - minimum 100/136)
3. Has sufficient motor ability/dexterity to use the kit or a carer who will be able to assist with the use of the kit.
4. Can tolerate light and have sufficient head control to wear the head set.
5. English speaking
Exclusion Criteria
2. Unable to tolerate light/unable to wear the head set
3. Light sensitive epilepsy, severe vertigo or dizziness.
4. Non English speaking
18 Years
80 Years
ALL
No
Sponsors
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Lancashire Teaching Hospitals NHS Foundation Trust
OTHER
Responsible Party
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Principal Investigators
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Malabika Ghosh, PhD
Role: PRINCIPAL_INVESTIGATOR
Lancashire Teaching Hospitals NHS Foundation Trust
Locations
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Lancashire Teaching Hospitals NHS Foundation Trust
Preston, , United Kingdom
Countries
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Provided Documents
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Document Type: Study Protocol
Other Identifiers
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274505
Identifier Type: -
Identifier Source: org_study_id
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