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Evaluation of a Specialized Yoga Program for Persons With Spinal Cord Injury (SCI)

Evaluation of a Specialized Yoga Program for Persons With Spinal Cord Injury: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02656927
Acronym
SCI
Enrollment
22
Registered
2016-01-15
Start date
2016-05-31
Completion date
2016-07-31
Last updated
2016-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injury

Keywords

Spinal Cord Injury, Yoga, Psychological Flexibility, Mindfulness, Pain

Brief summary

The purpose of this randomized controlled study is to evaluate psychological variables, mindfulness, and pain in the context of a specialized yoga program for individuals with SCI. Participants will be randomized to either a wait-list control condition or to a specialized yoga program condition.

Interventions

BEHAVIORALYoga Condition

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. have an SCI or a spinal related condition, 2. be 18 years of age or older, 3. be able to speak and read English, 4. commit to two weekly, one hour yoga classes for six weeks, 5. be referred from a clinician on the inter-disciplinary team, 6. have a sitting tolerance of one hour, 7. be able to participate in gentle physical activity in that time, 8. be aware of and understand his/her health contraindications (is able to practice safely), 9. provide a note from their physician indicating that it is safe for them to participate in a physical activity intervention, such as yoga.

Exclusion criteria

1. are not medically stable, 2. have pre-existing medical contraindications, 3. have cognitive limitations or language comprehension issues that would impact participation (determined by care team), 4. have had a regular yoga practice in the last six months.

Design outcomes

Primary

MeasureTime frame
Acceptance and Action Questionnaire-II (AAQ-II)Change from Baseline, 6 weeks, 12 weeks

Secondary

MeasureTime frame
General Self-Efficacy Scale (GSES)Change from Baseline, 6 weeks, 12 weeks
Post-Traumatic Growth Inventory-SF (PTGI-SF)Change from Baseline, 6 weeks, 12 weeks
Connor-Davidson Resilience Scale-10 Item (CS-RISC-10)Change from Baseline, 6 weeks, 12 weeks
Hospital Anxiety and Depression Scale (HADS)Change from Baseline, 6 weeks, 12 weeks
Self-Compassion Scale-SF (SCS-SF)Change from Baseline, 6 weeks, 12 weeks
Brief Pain Inventory-SF (BPI-SF)Change from Baseline, 6 weeks, 12 weeks
Pain Catastrophizing Scale (PCS)Change from Baseline, 6 weeks, 12 weeks
Five Facet Mindfulness Questionnaire-SF (FFMQ-SF)Change from Baseline, 6 weeks, 12 weeks

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026