Online Yoga and the Impact on Psychosis

June 13, 2022 updated by: The Royal Ottawa Mental Health Centre

Exploring the Impact of Online Yoga on Outcome and Recovery in People With Psychosis.

Yoga and mindfulness are considered complementary and alternative healthcare options that involve breathing techniques, relaxation, and bodily postures (yoga only). Research has shown a positive effect of these on depression, quality of life, and other symptoms of psychosis. As an 8-week pilot study, the goal is to offer yoga and/or mindfulness online and to explore the effect on recovery and quality of life for people with psychosis.

Study Overview

Status

Recruiting

Conditions

Detailed Description

Psychosis impacts about 3% of Canadians at any given time. People with psychosis can experience a combination of positive (e.g., delusions; hallucinations), negative (e.g., amotivation; reduced social activity), or cognitive symptoms (e.g., poorer memory; executive functioning). Positive symptoms are managed via antipsychotic medication and therapeutic support; cognitive symptoms can be targeted via cognitive remediation therapy. For negative symptoms, especially those idiopathic, there are still no effective care options. Yoga is a complementary and alternative medicine (CAM) encompassing health modalities of Eastern cultures, it involves breathing techniques, relaxation, and bodily postures. Research has shown that yoga can improve levels of depression and quality of life, and even attenuate negative symptoms. Given the extensive health care expenditures and unmet care needs for negative symptoms, there is a growing need to consider CAMs, such as yoga, and accessibility of CAMs via online methods. As a pioneering study, this proposed pilot study aims to explore the effect of an 8-week (i.e., 8 sessions) online yoga program on recovery/outcome, with a focus on negative symptoms, for people with psychosis. The investigators aim to recruit 24 people with psychosis and randomly assign them to either the yoga (n=12) or a mindfulness group (n=12); mindfulness, in essence, is yoga without the physical aspect (i.e., poses). The investigators hypothesize that yoga will improve quality of life and attenuate symptom severity, with a larger effect on negative symptoms, above the effect of mindfulness. A nonclinical sample (n=12) will also be recruited to examine feasibility and for feedback purposes.

Study Type

Interventional

Enrollment (Anticipated)

36

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 Contact

Study Locations

    • Ontario
      • Ottawa, Ontario, Canada, K1Z7K4
        • Recruiting
        • The Royal Ottawa Mental Heatlh Centre
        • Contact:
          • Michael Bodnar, PhD

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

18 years to 85 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

For clinical participants:

  • primary diagnosis of a schizophrenia-spectrum disorder (schizophrenia, schizophreniform, schizoaffective) or related psychotic disorder (delusional, brief psychotic, paraphrenia, bipolar with psychotic features, major-depressive with psychotic features)
  • access to protected internet (i.e., home internet plugged or password protected wireless)
  • adequate space to do yoga (e.g., at least 2 feet around each side of the yoga mat)
  • able to speak and read English
  • competent and able to offer voluntary informed consent to participate

For non-clinical participants (healthy controls):

  • not diagnosed with or received care for any mental illness
  • access to protected internet (i.e., home internet plugged or password protected wireless)
  • adequate space to do yoga (e.g., at least 2 feet around each side of the yoga mat)
  • able to speak and read English
  • competent and able to offer voluntary informed consent to participate

Exclusion Criteria:

For clinical participants:

  • not clinically stable; that is, major change in primary medication (e.g., switching or stopping antipsychotic) or hospitalisation within the past 4 weeks prior to first contact
  • currently with a physical ailment that restricts light movement exercises for yoga or chair yoga

For non-clinical participants (healthy controls):

  • have a first-degree relative with psychosis (schizophrenia, schizo-affective, schizophreniform, paraphrenia, brief psychotic, delusional, or bipolar or major depressive disorder with psychotic features)
  • had a substance or alcohol abuse/dependence in the past 6 months
  • currently with a physical ailment that restricts light movement exercises for yoga or chair yoga

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: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Clinical
Clinical participants with a primary diagnosis of psychosis or related disorder.
8 weeks of online weekly yoga or chair yoga class
8 weeks of online weekly mindfulness class
ACTIVE_COMPARATOR: Non-clinical
Non-clinical participants with no mental health diagnoses.
8 weeks of online weekly yoga or chair yoga class
8 weeks of online weekly mindfulness class

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline on the Clinical Outcomes in Routine Evaluation (CORE-10) scale at week 4
Time Frame: Baseline and Week 4
The CORE-10 is a self-reported instrument measuring levels of psychological distress in the past week. Possible scores range from 0 (not at all) to 4 (most or all of the time). Higher score = worse outcome. Change = (week 4 - baseline).
Baseline and Week 4
Change from baseline on the Clinical Outcomes in Routine Evaluation (CORE-10) scale at week 8
Time Frame: Baseline and Week 8
The CORE-10 is a self-reported instrument measuring levels of psychological distress in the past week. Possible scores range from 0 (not at all) to 4 (most or all of the time). Higher score = worse outcome. Change = (week 8 - baseline).
Baseline and Week 8
Change from baseline on the Clinical Outcomes in Routine Evaluation (CORE-10) scale at week 12
Time Frame: Baseline and Week 12
The CORE-10 is a self-reported instrument measuring levels of psychological distress in the past week. Possible scores range from 0 (not at all) to 4 (most or all of the time). Higher score = worse outcome. Change = (week 12 - baseline).
Baseline and Week 12
Change from baseline on the Clinical Outcomes in Routine Evaluation (CORE-10) scale at 6 months
Time Frame: Baseline and 6 Months
The CORE-10 is a self-reported instrument measuring levels of psychological distress in the past week. Possible scores range from 0 (not at all) to 4 (most or all of the time). Higher score = worse outcome. Change = (6 month - baseline).
Baseline and 6 Months
Change from baseline on the Positive and Negative Syndrome Scale for Schizophrenia (PANSS) scale at 4 weeks
Time Frame: Baseline and Week 4
The PANSS is a clinician-rated, semi-structured interview assessing schizophrenia symptom severity over the past week. Possible scores range from 1 (absent) to 7 (extreme). Higher score = worse outcome. Change = (week 4 - baseline).
Baseline and Week 4
Change from baseline on the Positive and Negative Syndrome Scale for Schizophrenia (PANSS) scale at 8 weeks
Time Frame: Baseline and Week 8
The PANSS is a clinician-rated, semi-structured interview assessing schizophrenia symptom severity over the past week. Possible scores range from 1 (absent) to 7 (extreme). Higher score = worse outcome. Change = (week 8 - baseline).
Baseline and Week 8
Change from baseline on the Positive and Negative Syndrome Scale for Schizophrenia (PANSS) scale at 12 weeks
Time Frame: Baseline and Week 12
The PANSS is a clinician-rated, semi-structured interview assessing schizophrenia symptom severity over the past week. Possible scores range from 1 (absent) to 7 (extreme). Higher score = worse outcome. Change = (week 12 - baseline).
Baseline and Week 12
Change from baseline on the Positive and Negative Syndrome Scale for Schizophrenia (PANSS) scale at 6 months
Time Frame: Baseline and 6 Months
The PANSS is a clinician-rated, semi-structured interview assessing schizophrenia symptom severity over the past week. Possible scores range from 1 (absent) to 7 (extreme). Higher score = worse outcome. Change = (6 month - baseline).
Baseline and 6 Months
Change from baseline on the Questionnaire about the Process of Recovery - Version 2 (QPR-2) scale at week 4
Time Frame: Baseline and Week 4
The QPR-2 is a self-reported instrument assessing levels of recovery over the past week. Scores range from 0 (disagree strongly) to 4 (agree strongly). Higher score = better outcome. Change = (week 4 - baseline).
Baseline and Week 4
Change from baseline on the Questionnaire about the Process of Recovery - Version 2 (QPR-2) scale at week 8
Time Frame: Baseline and Week 8
The QPR-2 is a self-reported instrument assessing levels of recovery over the past week. Scores range from 0 (disagree strongly) to 4 (agree strongly). Higher score = better outcome. Change = (week 8 - baseline).
Baseline and Week 8
Change from baseline on the Questionnaire about the Process of Recovery - Version 2 (QPR-2) scale at week 12
Time Frame: Baseline and Week 12
The QPR-2 is a self-reported instrument assessing levels of recovery over the past week. Scores range from 0 (disagree strongly) to 4 (agree strongly). Higher score = better outcome. Change = (week 12 - baseline).
Baseline and Week 12
Change from baseline on the Questionnaire about the Process of Recovery - Version 2 (QPR-2) scale at 6 months
Time Frame: Baseline and 6 Months
The QPR-2 is a self-reported instrument assessing levels of recovery over the past week. Scores range from 0 (disagree strongly) to 4 (agree strongly). Higher score = better outcome. Change = (6 months - baseline).
Baseline and 6 Months
Change from baseline on the Self-Evaluation of Negative Symptoms (SNS) scale at week 4
Time Frame: Baseline and Week 4
The SNS is a self-reported instrument assessing negative symptom severity over the past week. Possible answers are strongly agree, somewhat agree, strongly disagree. Higher score = worse outcome. Change = (week 4 - baseline).
Baseline and Week 4
Change from baseline on the Self-Evaluation of Negative Symptoms (SNS) scale at week 8
Time Frame: Baseline and Week 8
The SNS is a self-reported instrument assessing negative symptom severity over the past week. Possible answers are strongly agree, somewhat agree, strongly disagree. Higher score = worse outcome. Change = (week 8 - baseline).
Baseline and Week 8
Change from baseline on the Self-Evaluation of Negative Symptoms (SNS) scale at week 12
Time Frame: Baseline and Week 12
The SNS is a self-reported instrument assessing negative symptom severity over the past week. Possible answers are strongly agree, somewhat agree, strongly disagree. Higher score = worse outcome. Change = (week 12 - baseline).
Baseline and Week 12
Change from baseline on the Self-Evaluation of Negative Symptoms (SNS) scale at 6 months
Time Frame: Baseline and 6 Months
The SNS is a self-reported instrument assessing negative symptom severity over the past week. Possible answers are strongly agree, somewhat agree, strongly disagree. Higher score = worse outcome. Change = (6 months - baseline).
Baseline and 6 Months
Change from baseline on the Birchwood Insight Scale (BIS) scale at week 4
Time Frame: Baseline and Week 4
The BIS is a self-reported instrument assessing levels of insight without a specific time period. Possible answers are agree, disagree, unsure. Higher score = better outcome. Change = (week 4 - baseline).
Baseline and Week 4
Change from baseline on the Birchwood Insight Scale (BIS) scale at week 8
Time Frame: Baseline and Week 8
The BIS is a self-reported instrument assessing levels of insight without a specific time period. Possible answers are agree, disagree, unsure. Higher score = better outcome. Change = (week 8 - baseline).
Baseline and Week 8
Change from baseline on the Birchwood Insight Scale (BIS) scale at week 12
Time Frame: Baseline and Week 12
The BIS is a self-reported instrument assessing levels of insight without a specific time period. Possible answers are agree, disagree, unsure. Higher score = better outcome. Change = (week 12 - baseline).
Baseline and Week 12
Change from baseline on the Birchwood Insight Scale (BIS) scale at 6 months
Time Frame: Baseline and 6 Months
The BIS is a self-reported instrument assessing levels of insight without a specific time period. Possible answers are agree, disagree, unsure. Higher score = better outcome. Change = (6 months - baseline).
Baseline and 6 Months
Change from baseline on the Short Warwick Edinburgh Mental Well-Being Scale (SWEMWBS) scale at week 4
Time Frame: Baseline and Week 4
The SWEMWBS is a self-reported instrument assessing levels of overall mental well-being over the past 2 weeks. Possible scores range from 1 (none of the time) to 5 (all of the time). Higher score = better outcome. Change = (week 4 - baseline).
Baseline and Week 4
Change from baseline on the Short Warwick Edinburgh Mental Well-Being Scale (SWEMWBS) scale at week 8
Time Frame: Baseline and Week 8
The SWEMWBS is a self-reported instrument assessing levels of overall mental well-being over the past 2 weeks. Possible scores range from 1 (none of the time) to 5 (all of the time). Higher score = better outcome. Change = (week 8 - baseline).
Baseline and Week 8
Change from baseline on the Short Warwick Edinburgh Mental Well-Being Scale (SWEMWBS) scale at week 12
Time Frame: Baseline and Week 12
The SWEMWBS is a self-reported instrument assessing levels of overall mental well-being over the past 2 weeks. Possible scores range from 1 (none of the time) to 5 (all of the time). Higher score = better outcome. Change = (week 12 - baseline).
Baseline and Week 12
Change from baseline on the Short Warwick Edinburgh Mental Well-Being Scale (SWEMWBS) scale at 6 months
Time Frame: Baseline and 6 Months
The SWEMWBS is a self-reported instrument assessing levels of overall mental well-being over the past 2 weeks. Possible scores range from 1 (none of the time) to 5 (all of the time). Higher score = better outcome. Change = (6 months - baseline).
Baseline and 6 Months
Change from baseline on the Modified Global Assessment of Functioning - Revised (M-GAF(R)) scale at week 4
Time Frame: Baseline and Week 4
The M-GAF(R) is a clinician-rated instrument assessing overall level of functioning over the past month. Score ranges from 1 (severely impaired) to 100 (superior functioning). Higher score = better outcome. Change = (week 4 - baseline).
Baseline and Week 4
Change from baseline on the Modified Global Assessment of Functioning - Revised (M-GAF(R)) scale at week 8
Time Frame: Baseline and Week 8
The M-GAF(R) is a clinician-rated instrument assessing overall level of functioning over the past month. Score ranges from 1 (severely impaired) to 100 (superior functioning). Higher score = better outcome. Change = (week 8 - baseline).
Baseline and Week 8
Change from baseline on the Modified Global Assessment of Functioning - Revised (M-GAF(R)) scale at week 12
Time Frame: Baseline and Week 12
The M-GAF(R) is a clinician-rated instrument assessing overall level of functioning over the past month. Score ranges from 1 (severely impaired) to 100 (superior functioning). Higher score = better outcome. Change = (week 12 - baseline).
Baseline and Week 12
Change from baseline on the Modified Global Assessment of Functioning - Revised (M-GAF(R)) scale at 6 months
Time Frame: Baseline and 6 Months
The M-GAF(R) is a clinician-rated instrument assessing overall level of functioning over the past month. Score ranges from 1 (severely impaired) to 100 (superior functioning). Higher score = better outcome. Change = (6 months - baseline).
Baseline and 6 Months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Michael Bodnar, PhD, The Royal Ottawa Mental Health Centre

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

November 11, 2021

Primary Completion (ANTICIPATED)

November 5, 2022

Study Completion (ANTICIPATED)

November 5, 2022

Study Registration Dates

First Submitted

June 15, 2021

First Submitted That Met QC Criteria

September 15, 2021

First Posted (ACTUAL)

September 16, 2021

Study Record Updates

Last Update Posted (ACTUAL)

June 16, 2022

Last Update Submitted That Met QC Criteria

June 13, 2022

Last Verified

September 1, 2021

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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