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Not yet recruiting NCT07248345

Virtual Reality Intervention for Family Caregivers of Persons Living With Dementia

No phase Interventional Dementia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: virtual reality intervention.
Who it may be relevant to
Registry conditions: Dementia. Basic parameters: 18 years — 120 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

A Machine Learning-enhanced Virtual Reality Intervention to Facilitate Balance Finding for Family Caregivers of Persons Living With Dementia

Overview

This study explores the effects of a virtual reality intervention on family caregivers of persons living with dementia

Detailed description

Virtual interventions using VR scenarios related to competing demands for family caregivers of persons living with dementia that facilitate caregiving balance will be developed. Tts effects will be investigated by using a randomized controlled trial.

Interventions

  • Behavioral virtual reality intervention
    virtual interventions using VR scenarios related to competing demands for family caregivers of PLWD

Primary outcome measures

  • Caregiving Balance [Time frame: 1st month follwing VR intervention]
  • Caregiving Balance [Time frame: 3rd month follwing VR intervention]
  • Caregiving Balance [Time frame: 6th month follwing VR intervention]
  • Caregiver role strain [Time frame: 1st month following VR intervention]
  • Caregiver role strain [Time frame: 3rd month following VR intervention]
  • Caregiver role strain [Time frame: 6th month following VR intervention]
Secondary outcome measures (9)
  • Health Related Quality of Life [Time frame: 1st month following VR intervention]
  • Health Related Quality of Life [Time frame: 3rd month following VR intervention]
  • Health Related Quality of Life [Time frame: 6th month following VR intervention]
  • Depressive symptoms [Time frame: 1st month following VR intervention]
  • Depressive symptoms [Time frame: 3rd month following VR intervention]
  • Depressive symptoms [Time frame: 6th month following VR intervention]
  • Caregiving Rewards [Time frame: 1st month following VR intervention]
  • Caregiving Rewards [Time frame: 3rd month following VR intervention]
  • Caregiving Rewards [Time frame: 6th month following VR intervention]

Eligibility criteria

Inclusion criteria

\- has the primary responsibility for providing direct care or supervising the care received by the PLWD, and is living with the PLWD.

Exclusion criteria

\-

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Health services research

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07248345 · 114-2314-B-182-048-MY3

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗