Chair Yoga for Stress in Dementia

September 8, 2020 updated by: Soham Rej MD, MSc, Lady Davis Institute

Effectiveness of a Dyadic Chair Yoga Intervention for Reducing Stress in Patients With Dementia and Their Caregivers

Dementia is widely prevalent and results in high direct and indirect health costs. Dementia is associated with stress, anxiety, and depression in both patients and caregivers, and caregiver burden is extremely common. Treatment protocols for patients and caregivers are unclear and insufficient; drug treatments to manage behavioural and psychological symptoms of dementia can yield serious negative side effects, and caregivers may not have access to one-on-one psychotherapy due to high costs and long wait times. Yoga is an ancient Indian mind-body practice that uses physical postures, breathing exercises, and meditation. 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. Recent research has suggested that patients with dementia and their caregivers may also experience positive effects on their mental health from practicing yoga. Furthermore, when yoga is taught in a gentle and mindful manner, it is generally not associated with any negative side effects. While there is preliminary data on dyadic exercise interventions for dementia patients and their caregivers, to date no research has examined the effectiveness of a dyadic yoga intervention on stress, anxiety, and depression.

The investigators propose an 8-week study of a dyadic chair yoga program for patients with mild to moderate dementia and their caregivers (n = 30-40 participants). Our primary outcome of interest is changes in perceived stress, while secondary outcomes include changes in symptoms of depression and anxiety. The investigators will also look at the effects of the chair yoga program on caregiver burden, quality of interactions, well-being, mindfulness, and self-compassion. All outcomes will be assessed before the program starts and upon its termination. Participants will attend a 1-hour weekly group yoga class (4-10 participants per group) with their dyad for 8-weeks, and will also be given a video recording of a yoga class to practice together at home as often as possible. The investigators hypothesize that after the 8 week yoga program, patients and caregivers will report lower stress, as well as reduced symptoms of anxiety and depression. Results will be available mid-2020.

Study Overview

Status

Suspended

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Quebec
      • Montreal, Quebec, Canada, H4H 1R3
        • Douglas Mental Health University Institute
      • Montreal, Quebec, Canada, H3T 1E4
        • Institute of Community and Family Psychiatry

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients will have mild cognitive impairment or mild to moderate dementia (MMSE score between 10-26 inclusive) OR a diagnosis from his/her clinician of mild cognitive impairment or mild to moderate dementia
  • Patient and caregiver have contact at least 3 times per week
  • Either patient and/or caregiver will have a score of at least 10 on the PSS
  • Sufficient hearing to follow verbal instructions
  • Able to sit for 45 minutes without discomfort

Exclusion Criteria:

  • Patients will not have severe dementia (MMSE score < 10 OR diagnosis from his/her clinician)
  • Caregivers will not have dementia (MMSE score < 24)
  • Acute psychotic symptoms
  • Acute suicidal ideation or intent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in perceived stress scores as measured by the Perceived Stress Scale (PSS)
Time Frame: Baseline, 8-weeks

Using an 8-week single arm pilot trial, assess the effects of chair yoga on perceived stress in patients 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 gentle chair yoga program, patients with dementia and their caregivers will report lower perceived stress, as measured by the Perceived Stress Scale (PSS)

Baseline, 8-weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in depressive symptoms as measured by the Patient Health Questionnaire (PHQ-9)
Time Frame: Baseline, 8-weeks

Using an 8-week single arm pilot trial, assess the effects of chair yoga on patient and caregiver depressive symptoms using the PHQ-9.

Scores on the PHQ-9 can range from 0-27, with higher scores indicating more severe depression.

Hypothesis: Patients with dementia and their caregivers will report less severe symptoms of depression, as measured by the full version of the Patient Health Questionnaire (PHQ-9), following participation in an 8-week gentle chair yoga program.

Baseline, 8-weeks
Changes in symptoms of anxiety as measured by the Generalized Anxiety Disorder 7-item scale (GAD-7)
Time Frame: Baseline, 8-weeks

Using an 8-week single arm pilot trial, assess the effects of chair yoga on symptoms of anxiety in patients and caregivers using the GAD-7.

Scores on the GAD-7 range from 0-21, with higher scores indicating more severe anxiety.

Hypothesis: Patients with dementia and/or their caregivers will report fewer symptoms of anxiety, as measured by the Generalized Anxiety Disorder 7-Item Scale (GAD-7), following participation in an 8-week gentle chair yoga program.

Baseline, 8-weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in caregiver burden as measured by the Zarit Burden Inventory (ZBI)
Time Frame: Baseline, 8-weeks

Assess the effects of chair yoga on caregiver burden using the ZBI following 8 weeks of chair yoga.

Scores on the ZBI can range from 0-88, with higher scores corresponding to higher levels of burden.

Hypothesis 1: Caregivers of patients with dementia will report lower caregiver burden, as measured by the Zarit Burden Scale (ZBI), following participation in an 8-week gentle chair yoga program.

Hypothesis 2: Lower patient scores on the PHQ-9 and GAD-7 (week 8) will be associated with decreased caregiver burden following participation in an 8-week gentle chair yoga program.

Baseline, 8-weeks
Changes in relationship closeness as measured by the Whitlatch Relationship Closeness Scale
Time Frame: Baseline, 8-weeks

Assess the effects of chair yoga on levels of caregiver-rated relationship closeness using the Whitlatch Relationship Closeness Scale.

Scores on the Whitlatch Relationship Closeness Scale range from 0-24, with higher scores indicating closer relationships.

Baseline, 8-weeks
Changes in well-being as measured by the 12-Item Well-Being Questionnaire (W-BQ12)
Time Frame: Baseline, 8-weeks

Assess the effects of 8-weeks of chair yoga on patient and caregiver well-being using the W-BQ12.

Scores on the W-BQ12 range from 0-72, with higher scores indicating a greater sense of well-being.

Baseline, 8-weeks
Changes in levels of mindfulness as measured by the Five Facet Mindfulness Questionnaire (FFMQ-short form)
Time Frame: Baseline, 8-weeks

Assess the effects of 8 weeks of chair yoga on patient and caregiver levels of mindfulness using the short form of the FFMQ.

Scores on the short-form of the Five Facet Mindfulness Scale range from 0-120, with higher scores indicating higher levels of mindfulness.

Baseline, 8-weeks
Changes in levels of self-compassion as measured by the Self-Compassion Scale (SCS-short form)
Time Frame: Baseline, 8-weeks

Assess the effects of 8 weeks of chair yoga on patient and caregiver levels of self-compassion using the short form of the SCS.

Scores on the short for of the SCS range from 0-60, with higher scores indicating higher levels of self-compassion.

Baseline, 8-weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 27, 2020

Primary Completion (ANTICIPATED)

January 1, 2021

Study Completion (ANTICIPATED)

January 1, 2022

Study Registration Dates

First Submitted

October 29, 2019

First Submitted That Met QC Criteria

November 11, 2019

First Posted (ACTUAL)

November 14, 2019

Study Record Updates

Last Update Posted (ACTUAL)

September 10, 2020

Last Update Submitted That Met QC Criteria

September 8, 2020

Last Verified

September 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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