Online Yoga and the Impact on Psychosis

Sponsor
The Royal Ottawa Mental Health Centre (Other)
Overall Status
Recruiting
CT.gov ID
NCT05046912
Collaborator
(none)
36
1
2
11.8
3.1

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Yoga
  • Behavioral: Mindfulness
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Clinical and non-clinical participants will be assigned to either a yoga or mindfulness condition.Clinical and non-clinical participants will be assigned to either a yoga or mindfulness condition.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Exploring the Impact of Online Yoga on Outcome and Recovery in People With Psychosis.
Actual Study Start Date :
Nov 11, 2021
Anticipated Primary Completion Date :
Nov 5, 2022
Anticipated Study Completion Date :
Nov 5, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Clinical

Clinical participants with a primary diagnosis of psychosis or related disorder.

Behavioral: Yoga
8 weeks of online weekly yoga or chair yoga class

Behavioral: Mindfulness
8 weeks of online weekly mindfulness class

Active Comparator: Non-clinical

Non-clinical participants with no mental health diagnoses.

Behavioral: Yoga
8 weeks of online weekly yoga or chair yoga class

Behavioral: Mindfulness
8 weeks of online weekly mindfulness class

Outcome Measures

Primary Outcome Measures

  1. Change from baseline on the Clinical Outcomes in Routine Evaluation (CORE-10) scale at week 4 [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).

  2. Change from baseline on the Clinical Outcomes in Routine Evaluation (CORE-10) scale at week 8 [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).

  3. Change from baseline on the Clinical Outcomes in Routine Evaluation (CORE-10) scale at week 12 [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).

  4. Change from baseline on the Clinical Outcomes in Routine Evaluation (CORE-10) scale at 6 months [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).

  5. Change from baseline on the Positive and Negative Syndrome Scale for Schizophrenia (PANSS) scale at 4 weeks [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).

  6. Change from baseline on the Positive and Negative Syndrome Scale for Schizophrenia (PANSS) scale at 8 weeks [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).

  7. Change from baseline on the Positive and Negative Syndrome Scale for Schizophrenia (PANSS) scale at 12 weeks [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).

  8. Change from baseline on the Positive and Negative Syndrome Scale for Schizophrenia (PANSS) scale at 6 months [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).

  9. Change from baseline on the Questionnaire about the Process of Recovery - Version 2 (QPR-2) scale at week 4 [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).

  10. Change from baseline on the Questionnaire about the Process of Recovery - Version 2 (QPR-2) scale at week 8 [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).

  11. Change from baseline on the Questionnaire about the Process of Recovery - Version 2 (QPR-2) scale at week 12 [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).

  12. Change from baseline on the Questionnaire about the Process of Recovery - Version 2 (QPR-2) scale at 6 months [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).

  13. Change from baseline on the Self-Evaluation of Negative Symptoms (SNS) scale at week 4 [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).

  14. Change from baseline on the Self-Evaluation of Negative Symptoms (SNS) scale at week 8 [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).

  15. Change from baseline on the Self-Evaluation of Negative Symptoms (SNS) scale at week 12 [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).

  16. Change from baseline on the Self-Evaluation of Negative Symptoms (SNS) scale at 6 months [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).

  17. Change from baseline on the Birchwood Insight Scale (BIS) scale at week 4 [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).

  18. Change from baseline on the Birchwood Insight Scale (BIS) scale at week 8 [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).

  19. Change from baseline on the Birchwood Insight Scale (BIS) scale at week 12 [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).

  20. Change from baseline on the Birchwood Insight Scale (BIS) scale at 6 months [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).

  21. Change from baseline on the Short Warwick Edinburgh Mental Well-Being Scale (SWEMWBS) scale at week 4 [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).

  22. Change from baseline on the Short Warwick Edinburgh Mental Well-Being Scale (SWEMWBS) scale at week 8 [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).

  23. Change from baseline on the Short Warwick Edinburgh Mental Well-Being Scale (SWEMWBS) scale at week 12 [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).

  24. Change from baseline on the Short Warwick Edinburgh Mental Well-Being Scale (SWEMWBS) scale at 6 months [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).

  25. Change from baseline on the Modified Global Assessment of Functioning - Revised (M-GAF(R)) scale at week 4 [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).

  26. Change from baseline on the Modified Global Assessment of Functioning - Revised (M-GAF(R)) scale at week 8 [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).

  27. Change from baseline on the Modified Global Assessment of Functioning - Revised (M-GAF(R)) scale at week 12 [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).

  28. Change from baseline on the Modified Global Assessment of Functioning - Revised (M-GAF(R)) scale at 6 months [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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Royal Ottawa Mental Heatlh Centre Ottawa Ontario Canada K1Z7K4

Sponsors and Collaborators

  • The Royal Ottawa Mental Health Centre

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
The Royal Ottawa Mental Health Centre
ClinicalTrials.gov Identifier:
NCT05046912
Other Study ID Numbers:
  • 2021021
First Posted:
Sep 16, 2021
Last Update Posted:
Jun 16, 2022
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The Royal Ottawa Mental Health Centre
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 16, 2022