Observational studyPain research & management2017
Development and Implementation of a Registry of Patients Attending Multidisciplinary Pain Treatment Clinics: The Quebec Pain Registry.
Observational study in Pain research & management, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
30 citing papers in PubMed.
- A scoping review on the characteristics of chronic pain registries.Pain reports · 2026Review
- Patient Subgroups and Predictors of Improvement in Chronic Neuropathic Pain: A Trajectory-Based Analysis.European journal of pain (London, England) · 2025Article
- A sex- and gender-based analysis plus of frequent healthcare utilization among individuals living with chronic pain: a cohort study.BMC health services research · 2025Article
- Pain Management Strategies and Adverse Effects of Opioids in Patients with Neurotrauma with Acute and Chronic Pain.Neurotrauma reports · 2025Article
- Middle East Pain Registry (MEPAIN): Feasibility Study of Chronic Pain Registry and Pilot Phase Results : Middle East Pain Registry (MEPAIN).Galen medical journal · 2025Article
- Pain relief and associated factors: a cross-sectional observational web-based study in a Quebec cohort of persons living with chronic pain.Frontiers in pain research (Lausanne, Switzerland) · 2024Article
- Where we live matters: a comparison of chronic pain treatment between remote and non-remote regions of Quebec, Canada.Frontiers in pain research (Lausanne, Switzerland) · 2024Article
- Polypharmacy and Excessive Polypharmacy Among Persons Living with Chronic Pain: A Cross-Sectional Study on the Prevalence and Associated Factors.Journal of pain research · 2023Article
- Co-designing a Canadian adaptation of a lifestyle-oriented intervention aimed to improve daily functioning of individuals living with chronic pain: a multi-method study protocol of REVEAL(OT) Canada.Frontiers in rehabilitation sciences · 2023Article
- Examining the roles of depression, pain catastrophizing, and self-efficacy in quality of life changes following chronic pain treatment.Canadian journal of pain = Revue canadienne de la douleur · 2023Article
- The core minimum dataset for measuring pain outcomes in pain services across Scotland. Developing and testing a brief multi-dimensional questionnaire.British journal of pain · 2022Article
- Patient registries in orthopedics and orthobiologic procedures: a narrative review.BMC musculoskeletal disorders · 2022Review
- Gender Differences in Medication Adverse Effects Experienced by People Living With Chronic Pain.Frontiers in pain research (Lausanne, Switzerland) · 2022Article
- Pain Management Strategies After Orthopaedic Trauma: A Mixed-Methods Study with a View to Optimizing Practices.Journal of pain research · 2022Article
- Characteristics of Persons Seeking Care for Moderate to Severe Pain Due to Chronic Low Back Pain and Osteoarthritis: A Cross-Sectional Study.Journal of pain research · 2022Article
- Prevalence of cannabis use for pain management in Quebec: A post-legalization estimate among generations living with chronic pain.Canadian journal of pain = Revue canadienne de la douleur · 2022Article
- Demographics, Pain Characteristics and Diagnostic Classification Profile of Chronic Non-Cancer Pain Patients Attending a Canadian University-Affiliated Community Pain Clinic.Pain and therapy · 2021Article
- Determining chronic pain data elements as a first step towards improving quality of care and research in chronic pain.Acta bio-medica : Atenei Parmensis · 2021Article
- Chronic pain patients' willingness to share personal identifiers on the web for the linkage of medico-administrative claims and patient-reported data: The chronic pain treatment cohort.Pharmacoepidemiology and drug safety · 2021Article
- Cluster analysis of Canadian Armed Forces veterans living with chronic pain: Life After Service Studies 2016.Canadian journal of pain = Revue canadienne de la douleur · 2021Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
21 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The Quebec Pain Registry (QPR) is a large research database of patients suffering from various chronic pain (CP) syndromes who were referred to one of five tertiary care centres in the province of Quebec (Canada). Patients were monitored using common demographics, identical clinical descriptors, and uniform validated outcomes. This paper describes the development, implementation, and research potential of the QPR. Between 2008 and 2013, 6902 patients were enrolled in the QPR, and data were collected prior to their first visit at the pain clinic and six months later. More than 90% of them (mean age ± SD: 52.76 ± 4.60, females: 59.1%) consented that their QPR data be used for research purposes. The results suggest that, compared to patients with serious chronic medical disorders, CP patients referred to tertiary care clinics are more severely impaired in multiple domains including emotional and physical functioning. The QPR is also a powerful and comprehensive tool for conducting research in a "real-world" context with 27 observational studies and satellite research projects which have been completed or are underway. It contains data on the clinical evolution of thousands of patients and provides the opportunity of answering important research questions on various aspects of CP (or specific pain syndromes) and its management.
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Registered trials
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