NCT04162964

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2020

Geographic Reach
1 country

2 active sites

Status
terminated

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

Completed
16 days until next milestone

First Posted

Study publicly available on registry

November 14, 2019

Completed
2 months until next milestone

Study Start

First participant enrolled

January 27, 2020

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 13, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 13, 2021

Completed
Last Updated

April 16, 2025

Status Verified

September 1, 2020

Enrollment Period

1.1 years

First QC Date

October 29, 2019

Last Update Submit

April 11, 2025

Conditions

Keywords

DementiaStressCaregivingMind-body therapyAnxietyDepression

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

EXPERIMENTAL
Behavioral: Virtual Chair Yoga

Waitlist Control Group

PLACEBO COMPARATOR
Behavioral: Virtual Chair Yoga

Interventions

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.

Chair Yoga TreatmentWaitlist Control Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Douglas Mental Health University Institute

Montreal, Quebec, H4H 1R3, Canada

Location

MeSH Terms

Conditions

DementiaAnxiety DisordersDepression

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System DiseasesNeurocognitive DisordersMental DisordersBehavioral SymptomsBehavior

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

Locations