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Online Mindfulness-based Stress Reduction Intervention for People With Chronic Pain Waiting for Health Services

Online Mindfulness-based Stress Reduction Intervention for Chronic Pain in Individuals Waiting for Health Care Services: a Study Protocol for a Pilot Randomized Controlled Trial (RCT)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04842097
Enrollment
60
Registered
2021-04-13
Start date
2021-06-16
Completion date
2022-01-24
Last updated
2022-09-22

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

Conditions

Chronic Pain

Keywords

mindfulness-based stress reduction intervention

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

Interventions

BEHAVIORALMindfulness-based stress reduction

An online mindfulness-based stress reduction intervention will be administered in a group format of maximum 15 participants, once a week for 120 minutes for 8 weeks by an experienced therapist trained in MBSR. Sessions will include sitting and lying meditation, hatha yoga and a body scan where attention is sequentially focused on different parts of the body. Individual autonomous practice between 30-45 minutes, 6 times / week will also be recommended. To support individual autonomous practice, a daily diary and two guided videos (around 35 minutes/each) were created.

Sponsors

Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

It is not possible to blind the participants to group allocation due to the nature of the mindfulness-based stress reduction intervention; however, the outcome assessor, who will administer the outcome questionnaires to the participants will be blinded to the participants' group allocation as well the investigator and the data analyst who will conduct the analysis ensuring neutrality of the outcome assessment.

Intervention model description

A two group parallel single blind pilot RCT

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Participants retention rate2 monthsThe percentage of participants who have completed the 8 online MBSR sessions
Participants participation rate12 monthsThe percentage of participants on waiting lists who agreed to participate in the intervention

Secondary

MeasureTime frameDescription
French-Canadian Chronic Pain Self-Efficacy ScaleChange 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.
Chronic Pain Acceptance QuestionnaireChange 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.
Patient-Reported Outcomes Measurement Information System Global-10Change 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 ScaleChange 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.
Pain Disability IndexChange 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)
Global Rating of Change Scale3-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.
Patient-Reported Outcomes Measurement Information System 29Change 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.

Countries

Canada

Outcome results

None listed

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