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Not Yet Recruiting NCT07658287

Immersive Virtual Reality for Older Adults in Long-Term Care Settings

Conditions: Cognitive Impairment, Long-term Care Centres for Old Adults Users

Sex: All
Ages: 60 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 36
Sponsor: Laval University

Summary

The goal of this clinical trial is to learn if an immersive virtual reality mindfulness meditation program is feasible and acceptable for older adults living in long-term care settings in Quebec who have mild to moderate neurocognitive disorder. It will also learn about the safety and potential effects of the program on well-being. The main questions it aims to answer are: * Is the virtual reality mindfulness meditation program feasible and acceptable for residents and staff in long-term care settings? * Does the adapted version of the program show potential benefits for well-being, including depression, anxiety, quality of life, mindfulness, pain, and loneliness? * What practical challenges, user experiences, and side effects, such as cybersickness, occur during the program? Researchers will compare the original Toujours Dimanche virtual reality mindfulness meditation program, an adapted version of Toujours Dimanche designed for older adults with mild to moderate neurocognitive disorder, and standard care alone to see if the adapted program is feasible, acceptable, and potentially helpful. Participants will: * Take part in up to 8 virtual reality mindfulness meditation sessions over 4 weeks, if assigned to a virtual reality group * Complete questionnaires before and after the 4-week study period * Share feedback about their experience, when possible * Be observed by staff or research team members to document feasibility, acceptability, user experience, and safety

Eligibility Criteria

Inclusion Criteria: For resident participants: * Resident of a participating long-term care facility, seniors' home, or alternative seniors' home in the Chaudière-Appalaches or Capitale-Nationale regions of Quebec * Aged 60 years or older * Able to understand French or English * Able to provide informed consent or assent, or have consent provided by a legally authorized representative or person authorized to consent * Mild to moderate cognitive impairment or neurocognitive disorder * Normal or corrected vision and hearing For staff participants: * Regularly works with at least one resident participating in Phase 3 * Has completed the revised virtual reality training provided by Super Splendide and/or Martine Bordeleau Exclusion Criteria: For resident participants: * Recurrent migraines * Epilepsy * Traumatic brain injury during the past year * Glaucoma or recovery from eye surgery * Diagnosed uncontrolled epilepsy * Diagnosed severe vertigo * Severe hearing impairment without a corrective hearing device * Significant visual impairment that would prevent use of a virtual reality headset * Motion sickness that would prevent use of a virtual reality headset * Any health condition that restricts movement or prevents safe participation, such as a significant reduction in neck or upper-limb range of motion

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07658287). StuddyBuddy aggregates publicly available trial information.