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Effectiveness of Motorised Lumbar Support for Non-specific Low Back Pain

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Recruitment opened
    • Study sites: 0 to 1
    v3
  2. Start date: Jan 15, 2026 to Feb 16, 2026v2 Show 4 more changesShow less
    • Interventions: Motorized lumbar support (Other), Satic lumbar support (Other) to Motorized lumbar support (Other), Standard lumbar support (Other)
    • Eligibility criteria expanded, about 36 words
    • Secondary endpoints: details revised at 5 of 8 entries
    • Study description expanded, about 21 words
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Low back pain (LBP) represents a common musculoskeletal conditions worlwide, causing substantial disability and economic burden. While traditional semi-rigid lumbar supports are commonly prescribed to alleviate LBP symptoms, their effectiveness remains limited by their static mechanical properties and lack of adaptability to movement patterns. Motorized lumbar support offer a novel approach by allowing the application of controlled decompressive forces while maintaining functional mobility. This experimental study aims to compare the effectiveness between a motorized lumbar support and a standard semi-rigid support in adults with non-specific LBP. Seventy adults with non-specific low back pain (LBP) will be recruited. Primary outcomes (pain intensity and physical functioning \[daily average\]) will be collected daily, while secondary outcomes (average pain intensity over the last week, pain-related disability, etc.) will be assessed at baseline, 3 and 9 weeks after randomization.
Trial Details
NCT Number NCT07366827
Lead Sponsor Laval University
Collaborators: Corset Saint-Francis, MedTeq
Conditions
(from sponsor)		 Non-specific Low Back Pain
Enrollment 70 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov