Multimodal Intervention in Patients With Non-specific Chronic Low Back Pain: the HEALTHY BACK Project
CompletedNot applicableNCT06114264
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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)
Low back pain is one of the most common health problems seen in the primary care. Chronic low back pain is localized between the inferior limit of the ribs and the sacral region, and persist more than 12 weeks. In most cases, it is attributed to a non-specific cause and classified as non-specific chronic low back pain (NSCLBP). No previous study has included a multimodal supervised program in patients with NSCLBP. The primary aim of this study is to determine the effectiveness of exercise + behaviour change + education + mindfulness programs (intervention 1) and an intervention including intervention 1 following functional resistance training (Intervention 2) on endogenous pain modulation, disability, muscle strength/endurance, quality of life, gait parameters, levels of physical activity, sedentary behaviour and psychological health in patients with NSCLBP.
Study details
- Official title
- Multimodal Intervention to Improve Pain and Health in Patients With Non-specific Chronic Low Back Pain: the HEALTHY BACK Project
- Conditions
- Pain, Chronic
- Neurologic Manifestations
- Back Pain
- Low Back Pain
- Behavior, Health
- Interventions
- Behavioral: Multimodal + Resistance Programs
- Other: Control group
- Sponsor
- IBS Granada
- Collaborators
- University Hospital Virgen de las Nieves; Instituto de Salud Carlos III
- Start date
- 2023-01-01
- Primary completion
- 2025-04-30
- Sex
- All
- Age range
- from 18 Years to 65 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: * Be previously diagnosed with NSCLBP pain by a healthcare professional according to the criteria established by O'Sullivan et al1. * Intend to participate in the intervention and perform all the tests included in the study. * Able to read and understand informed consent, as well as the objective of the study. * Able to walk and move without outside help. * Able to communicate without problems. Exclusion Criteria: * Be under 20 years or over 65 years old. * Having acute or terminal illness. * Having medical prescription that prevents the performance of the tests. * Having injury or circumstance that makes it impossible to perform the tests correctly. * Having other physical or mental illness that prevents participating in the intervention.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06114264