Persistent Postoperative Pain
Conditions
Brief summary
This randomized controlled trial will evaluate a yoga intervention for individuals who experience persistent pain following oncology surgery. The integrated yoga program will involve postures, breathing exercises, and concentration practices. Data will be collected at several time points (pre-, mid-, and post-intervention) for both the intervention and wait-list control conditions. The data will be analysed using linear mixed effects growth models. Results will be written up in manuscript format, published in a peer review journal, and disseminated at scientific research conferences.
Interventions
BEHAVIORALYoga Condition
Participants randomized to the Yoga Condition will participate in an integrated yoga program consisting of yoga postures, breathing exercises, and concentration/meditation practices.
Sponsors
University Health Network, Toronto
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
1. Is a patient at specific pain clinics 2. Has undergone oncology surgery prior to commencing the yoga intervention 3. Is 18 years of age or older 4. Is able to speak and read English 5. Is able to commit to one weekly, one hour yoga classes for eight weeks 6. Is able to provide a note from their physician or kinesiologist indicating that it is safe for them to participate in a gentle physical activity intervention, such as yoga
Exclusion criteria
1. Has pre-existing medical contraindications that preclude participation 2. Has cognitive limitations or language comprehension issues that would impact participation 3. Have had a regular yoga practice in the last six months 4. Documented personality disorder 5. Pregnant women 6. Current enrollment in another research trial evaluating a mind-body intervention
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in scores on the Pain Catastrophizing Scale | at 0, 4 and 8 weeks |
Countries
Canada
Outcome results
None listed