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Clinical Trials/NCT05315609
NCT05315609
Completed
Not Applicable

Effects of Virtual Reality Meditation in Older Adults: A Randomized Controlled Trial

Lady Davis Institute2 sites in 1 country30 target enrollmentApril 30, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Older Adults
Sponsor
Lady Davis Institute
Enrollment
30
Locations
2
Primary Endpoint
Changes in stress scores as measured by the Perceived Stress Scale (PSS) for treatment group versus control group
Status
Completed
Last Updated
10 months ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
April 30, 2022
End Date
September 1, 2022
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Lady Davis Institute
Responsible Party
Principal Investigator
Principal Investigator

Soham Rej MD, MSc

Primary Investigator

Lady Davis Institute

Eligibility Criteria

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
  • 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

Outcomes

Primary Outcomes

Changes in stress scores as measured by the Perceived Stress Scale (PSS) for treatment group versus control group

Time Frame: Baseline, Once weekly during intervention

To assess the effectiveness of the virtual reality meditation program in reducing stress in older adults. Scores on the PSS can range from 0-40, with higher scores indicating higher perceived stress.

Secondary Outcomes

  • Changes in symptoms of anxiety as measured by the Generalized Anxiety Disorder-7 (GAD-7) questionnaire for treatment group versus control group(Baseline, Once weekly during intervention)
  • Changes in symptoms of depression as measured by the Patient Health Questionnaire-9 (PHQ-9) scale for treatment group versus control group(Baseline, Once weekly during intervention)

Study Sites (2)

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