Online MBSR Program for Cancer Survivors With Chronic Neuropathic Pain
CompletedNot applicableNCT02758197
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Brief summary (from the registry)
This randomized controlled trial will evaluate the effectiveness of an interdisciplinary treatment approach combining medical management with an online Mindfulness-Based Stress Reduction (MBSR) program in reducing disability and improving quality of life among cancer survivors living with moderate to severe chronic neuropathic pain.
Study details
- Official title
- The Effects of an Online Mindfulness-Based Stress Reduction (MBSR) Program on Quality of Life and Immune Function Among Cancer Survivors With Chronic Neuropathic Pain
- Conditions
- Cancer
- Painful Neuropathy
- Chronic Pain
- Worries
- Pain or Disability
- Interventions
- Behavioral: Mindfulness-Based Stress Reduction (MBSR)
- Sponsor
- Ottawa Hospital Research Institute
- Collaborators
- Canadian Cancer Society (CCS)
- Start date
- 2016-07
- Primary completion
- 2020-10
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- Canada
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * cancer survivors * experiencing cancer-related neuropathic pain symptoms for at least 3 months * pain severity ≥4/10 (moderate to severe) * ability to attend 7 out of 9 MBSR sessions * ability to complete questionnaires and attend sessions conducted in English or French * access to the internet and use of an electronic device capable of joining a video conference (i.e., computer or mobile device with a camera and microphone) Exclusion Criteria: * expected survival of less than 12 months * cognitive impairment * severe psychiatric disorder impacting ability to participate (e.g., schizophrenia, severe depression) * prior experience with MBSR
Canadian sites (1)
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02758197