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Effects of Virtual Reality Meditation in Older Adults

L

Lady Davis Institute

Status

Completed

Conditions

Mental Disorder
Older Adults
Stress

Treatments

Behavioral: VR Meditation

Study type

Interventional

Funder types

Other

Identifiers

NCT05315609
IUSMD-21-48

Details and patient eligibility

About

Virtual reality (VR) allows users to interact within a simulated environment using electronic devices such as a VR headset or goggles. Multiple studies with younger adults have demonstrated that VR meditation can be an important tool in reducing stress, however, this has not been studied in older adults. In this study, the investigators aim to assess the effects of a 4-week program of 15-minutes sessions, twice per week of meditation delivered through VR with the aim of evaluating its impact on stress in older adults.

Enrollment

30 patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Living in the Greater Montreal area and able to speak English or French
  • Perceived Stress Score (PSS)equal or greater than 10
  • Over >=60 years of age

Exclusion criteria

  • Diagnosis of epilepsy, schizophrenia, brain tumor
  • History of recurrent migraines or seizures or TBI in the past year
  • Substance use disorders in the last year
  • Psychiatric hospitalizations in the last year.
  • Acute psychotic symptoms
  • Acute suicidal ideation or intent
  • Glaucoma
  • PTSD
  • Changes to psychoactive medications in the past 4 weeks
  • Alcohol, caffeine or cannabis consumption within 24 hr before the session, or nicotine consumption within 15 min of the session
  • Important hearing impairment
  • Recovery phase of any eye surgery

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Intervention: Virtual Reality Mindfulness Group
Experimental group
Description:
The intervention will be 4-weeks, twice per week, 15-minute/session VR-mindfulness intervention group.
Treatment:
Behavioral: VR Meditation
No intervention: Waitlist Control Group
No Intervention group
Description:
These participants will be on a waitlist to receive the VR guided meditation program after data collection has been completed (after the 4 weeks)

Trial contacts and locations

2

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Central trial contact

Paola Lavín; Karin Cinalioglu

Data sourced from clinicaltrials.gov

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