Online Mindfulness-based Stress Reduction Intervention for People With Chronic Pain Waiting for Health Services
- Conditions
- Chronic Pain
- Interventions
- Behavioral: Mindfulness-based stress reduction
- Registration Number
- NCT04842097
- Lead Sponsor
- Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal
- Brief Summary
The goal of this project is to explore the feasibility and the efficacy of a online mindfulness-based stress reduction intervention for people with chronic pain waiting for secondary or tertiary health care services
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
- Men and women aged 18-85
- Self-reported diagnosis of chronic non-cancer pain
- Chronic non-cancer pain duration of 3 months or more
- Chronic non-cancer pain experienced during 4 days or more per week
- Average pain intensity of 4 or more out of 10 in the last seven days
- French or English fluency
- Access to Wi-Fi
- Be able to attend a weekly two-hour MBSR virtual session for eight consecutive weeks
- Cancer-related chronic pain
- Currently receiving or have received in the last 24 months coordinated care in pain clinics, hospitals or rehabilitation centers.
- Current or recent participation (in the last 12 months and more than 12 sessions) of cognitive-behavioral therapy or MBSR program
- Having an unstable psychological conditions such as depression, bipolar disorder, post-traumatic stress disorder, psychotic disorder
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Mindfulness-based stress reduction intervention Mindfulness-based stress reduction Online 8-week group program, once per week
- Primary Outcome Measures
Name Time Method Participants retention rate 2 months The percentage of participants who have completed the 8 online MBSR sessions
Participants participation rate 12 months The percentage of participants on waiting lists who agreed to participate in the intervention
- Secondary Outcome Measures
Name Time Method Patient-Reported Outcomes Measurement Information System 29 Change from week start of MBSR intervention (week 0) to end of intervention (week 8), 3-month follow-up (week 21) Change in 8 health-related quality of life domains as measured by the PROMIS 29. PROMIS-29 is a generic patient reported outcome measure, which includes four items from each of the seven PROMIS domains (physical function, depression, anxiety, fatigue, sleep disturbance, and ability to participate in social roles and activities, pain interference) and a single item on pain intensity. Each item has five response options (values 1 to 5), except for the pain intensity item which has eleven response options (values 0 to 10). A total raw score is computed for each domain as the sum of the response to each question within the domain, leading to seven domain scores, each from 4 to 20.
French-Canadian Chronic Pain Self-Efficacy Scale Change from week start of MBSR intervention (week 0) to end of intervention (week 8), 3-month follow-up (week 21) The French-Canadian Chronic Pain Self-Efficacy Scale (Lacasse et al., 2015) is a 6-item scale that measures an individual's confidence in his/her ability to manage chronic pain in general and pain-related symptoms. Items are rated on a 10-point Likert scale ranging from 1 = not at all confident to 10 = entirely confident. Score range is 6-60 with higher scores reflecting greater chronic pain self-efficacy.
Global Rating of Change Scale 3-month follow-up (week 21) The Global Change Rating Scale (11-point visual analogue scale raging from minus 5 to plus 5) will be used to assess the participants' perception of improvement (or decline) in relation to their self-efficacy in manging pain at the end of the MBSR intervention.
Chronic Pain Acceptance Questionnaire Change from week start of MBSR intervention (week 0) to end of intervention (week 8), 3-month follow-up (week 21) The Chronic Pain Acceptance Questionnaire (CPAQ-8; Fish et al., 2010 ) is an 8-item scale comprised of two subscales: activity engagement and pain willingness. Items are scored on a 7-point Likert scale ranging from 0 = never true to 6 = always true. Score range is 0-48 with increases in scores meaning better outcome.
Pain Disability Index Change from week start of MBSR intervention (week 0) to end of intervention (week 8), 3-month follow-up (week 21) Change in pain disability as measured by the The French-Canadian Pain Disability Index (score range is 0-70 with decreases in scores meaning better outcome)
Patient-Reported Outcomes Measurement Information System Global-10 Change from week start of MBSR intervention (week 0) to end of intervention (week 8), 3-month follow-up (week 21) Change in domains of health and functioning as measured by the PROMIS Global-10, score range is 7-35 with increases in scores meaning better outcome
Pain Catastrophizing Scale Change from week start of MBSR intervention (week 0) to end of intervention (week 8), 3-month follow-up (week 21) Change in pain catastrophizing as measured by the Pain Catastrophizing Scale (French Canadian version). PCS is a 13-item measure using a 5-point Likert scale (0=not at all, 4=all the time) with score range between 0-52 with decreases in scores meaning better outcome.
Trial Locations
- Locations (3)
Association québécoise de la douleur chronique
🇨🇦Montreal, Quebec, Canada
Hôpital de Verdun
🇨🇦Montreal, Quebec, Canada
Centre de réadaptation Layton-Lethbridge-Mackay
🇨🇦Montreal, Quebec, Canada