Effectiveness of Coping Strategies on the Control of Chronic Non-Cancer Pain and Quality of Life (CNCP_CopQol)
Unknown statusNot applicableNCT04696107
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
* Introduction and objectives: Non-pharmacological interventions in patients with musculoskeletal chronic non-cancer pain (mCNCP) are positioning themselves as an essential pillar in treatment along with pharmacological and interventional treatment. Training the patient in psycho-educational interventions focused on the neuroscience of pain and accompanying them towards a better coping of their disease can decrease the perception of pain and improve their quality of life. A previous pilot study, developed by the researchers about this type of interventions, identified as relevant data an improvement in the quality of life (QoL) of patients with mCNCP with a significant decrease in pharmacological consumption, and a high degree of satisfaction on the part of the user through the analysis of PROMs (patient-reported outcome measures). The main objective of this study is to know the effectiveness in the perception of pain through the Verbal Numerical Rating Scale (VNRS) and in the quality of life through the EuroQol-5D (EQ-5D) questionnaire of a psychoeducational intervention focused on emotional coping strategies, in patients with mCNCP in the Primary Care Centres of Public Health System of Aljarafe-Sevilla Norte Area (Spain). Secondarily, the consumption of health resources associated with mCNCP, the adherence to treatment, the influence of social, emotional, and family variables will be studied by the researchers in the two groups of patients on each telephone assessment. * Methodology: Prospective, randomized, triple-blind (patient, investigator, and analysis) and controlled clinical trial. Participants with mCNCP in follow-up in Primary Care without clinical control with the treatment scheduled and who agree to participate in the study will be randomized by blocks permuted to receive treatments and standard care (control group) or these same care plus a psychoeducational intervention (experimental group). This intervention consists of an emotional self-regulation t…
Study details
- Official title
- Effectiveness of Coping Strategies on the Control of Musculoskeletal Chronic Non-Cancer Pain and Quality of Life: A Randomized Clinical Trial
- Conditions
- Chronic Pain
- Musculoskeletal Diseases
- Quality of Life
- Pain Measurement
- Interventions
- Behavioral: Psychoeducative intervention
- Sponsor
- Hospital San Juan de Dios del Aljarafe de Sevilla
- Collaborators
- University of Seville; Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
- Start date
- 2021-04-01
- Primary completion
- 2022-02-28
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- Spain
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
INCLUSION CRITERIA: * People over the age of 18. * People with mCNCP served for this reason in the Primary Care Centres depend on Hospital San Juan de Dios del Aljarafe, who follow regular specific treatment on the WHO analgesic scale and who have accepted, after information and informed consent signature, their participation in this study. * Able to read and write Spanish. EXCLUSION CRITERIA: * Patients who have received interventional analgesic treatment in the year for the current disease. * Have followed program or maintain out-of-hospital therapy similar to the one this study focuses on. * Have had surgery or been on a waiting list during the study. * Severe or decompensated systemic disease. * Active cancer disease. * Psychiatric pathology, epilepsy or cognitive impairment. * Abuse drug addiction. * Accidents or new Injuries that may increase the perception of pain during the study. * Labor litigation due to pain. * Language barrier. LOSS CRITERIA: * Voluntary abandonment of the study. * Absence of one or more workshop sessions * Partial or complete loss of telephone follow-up. * Incomplete data collection. * Exitus. * Present any suspicious symptoms of COVID-19 disease collected by phone call the day before the workshop or communicate direct contact with a person infected in the previous days.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04696107