Study Stopped
COVID-19
Chair Yoga for Stress in Dementia
Effectiveness of a Virtual Chair Yoga Intervention for Reducing Stress in Older Adults With Dementia and Caregivers
1 other identifier
interventional
30
1 country
2
Brief Summary
Over 700,000 Canadians are affected by dementia costing the health care system approximately $10 billion/year. Due to COVID-19, the government has urged individuals over the age of 70 to stay home, putting this population at risk of social isolation. Older adults with mild cognitive impairments (MCIs), dementia, and their caregivers are at an even higher risk of becoming stressed, anxious, and agitated while in lockdown. Unsurprisingly, caregiver burden is extremely common, and often precedes institutionalization of the patient, as the demands of the illness begin to exceed that which the caregiver can sustainably provide. Since social distancing measures have shut down activities and support groups for these individuals, there is an urgent need for scalable, cost-effective, non-pharmacological interventions that can be delivered remotely to improve stress and loneliness. Yoga may be a viable therapeutic modality to address the psychological challenges associated with dementia in patients and caregivers, as it has been shown to decrease stress and improve anxiety and depressive symptoms in various populations. For this reason, we are conducting a randomized controlled trial (RCT) to assess the efficacy of an 8-week virtual chair yoga program to improve stress, psychological symptoms, and caregiver burden. This virtual chair yoga study will engage both older adults with dementia/MCI and caregivers (n=40-60 participants) during COVID-19, which is consistent with the need for decreasing costs and increasing accessibility of novel health interventions during and beyond the pandemic. We will evaluate the effect of this program on stress, loneliness, and mental health related outcomes such as fear of COVID-19, depression, anxiety, and caregiver burden compared to a waitlist control group. We will also be conducting a qualitative component in the form of semi-structured interviews. All quantitative outcomes will be assessed before the program starts and post-intervention and qualitative outcomes will be assessed post-intervention. Participants will be randomly assigned to the treatment group (virtual chair yoga 1 hour per week on Zoom) or the waitlist control group. The investigators hypothesize that after the 8-week yoga program, older adults and caregivers will report lower stress, loneliness, depression, anxiety, fear of COVID-19, and caregiver burden. Results will be available late-2021.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jan 2020
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 29, 2019
CompletedFirst Posted
Study publicly available on registry
November 14, 2019
CompletedStudy Start
First participant enrolled
January 27, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 13, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
March 13, 2021
CompletedApril 16, 2025
September 1, 2020
1.1 years
October 29, 2019
April 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Changes in perceived stress scores as measured by the Perceived Stress Scale (PSS) for treatment group versus control group
The 8-week randomized controlled trial (RCT) of the virtual chair yoga treatment versus the waitlist control group will assess the effects of the virtual chair yoga on perceived stress in older adults and caregivers, using the PSS. Scores on the PSS can range from 0-40, with higher scores indicating higher perceived stress. Hypothesis: Following participation in an 8-week RCT of the virtual chair yoga program, older adults with dementia and their caregivers will report lower perceived stress, as measured by the Perceived Stress Scale (PSS) compared to the waitlist control group.
Baseline, 8-weeks
Secondary Outcomes (1)
Changes in loneliness scores as measured by the 3-item UCLA Loneliness Scale for treatment group versus control group
Baseline, 8-weeks
Other Outcomes (5)
Changes in caregiver burden as measured by the Zarit Burden Interview (ZBI) for treatment group versus control group
Baseline, 8-weeks
Changes in depressive symptoms as measured by the Patient Health Questionnaire-9 (PHQ-9) for treatment group versus control group
Baseline, 8-weeks
Changes in symptoms of anxiety as measured by the Generalized Anxiety Disorder-7 (GAD-7) scale for treatment group versus control group
Baseline, 8-weeks
- +2 more other outcomes
Study Arms (2)
Chair Yoga Treatment
EXPERIMENTALWaitlist Control Group
PLACEBO COMPARATORInterventions
8-week virtual chair yoga program for one hour per week. Chair yoga is an effective way to offer modified yoga postures and relaxation techniques to individuals with limited mobility and/or advanced age for whom mat-based classes may not be accessible. The weekly yoga classes will be lead on the software Zoom by a certified instructor in English and French.
Eligibility Criteria
You may qualify if:
- Mild cognitive impairment or mild to moderate dementia (MoCA-BLIND score between 8-18 OR a diagnosis from his/her clinician of mild cognitive impairment) or mild to moderate dementia
- Sufficient hearing to follow verbal instructions
- Access to Zoom software and internet connection
- Ability to sit for 60 minutes without discomfort
- At least 60 years old
You may not qualify if:
- Severe dementia (MoCA-BLIND score \< 8)
- Acute psychotic symptoms
- Acute suicidal ideation or intent
- Resides outside of Quebec
- Providing care for someone with cognitive impairments (mild cognitive impairment or mild, moderate, or severe dementia)
- Sufficient hearing to follow verbal instructions
- Access to Zoom software and internet connection
- Ability to sit for 60 minutes without discomfort
- At least 18 years old
- Dementia (MoCA-BLIND score \< 18)
- Acute psychotic symptoms
- Acute suicidal ideation or intent
- Resides outside of Quebec
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Institute of Community and Family Psychiatry
Montreal, Quebec, H3T 1E4, Canada
Douglas Mental Health University Institute
Montreal, Quebec, H4H 1R3, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
October 29, 2019
First Posted
November 14, 2019
Study Start
January 27, 2020
Primary Completion
March 13, 2021
Study Completion
March 13, 2021
Last Updated
April 16, 2025
Record last verified: 2020-09
Data Sharing
- IPD Sharing
- Will not share