Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Sensory Stimulation Belt for Chronic Low Back Pain in Office Workers (LSS-BELT)

30 de agosto de 2026 atualizado por: Peemongkon Wattananon, Mahidol University

Effectiveness of a Sensory Stimulation Belt for Office Workers With Chronic Nonspecific Low Back Pain: A Double-Blind, Sham-Controlled Randomized Trial

This randomized, double-blind, sham-controlled trial will evaluate the effectiveness of a sensory stimulation belt in office workers with chronic nonspecific low back pain. Participants will first complete baseline clinical and sensorimotor assessments and will then be randomly assigned in a 1:1 ratio to receive either an active sensory stimulation belt or a sham belt.

Participants will wear the assigned belt during their usual office work for at least 4 hours per day, 5 days per week, for 4 weeks. Daily belt use, pain intensity, adherence, skin reactions, and device-related problems will be recorded in a study logbook, with weekly follow-up by the research team.

Clinical outcomes will include pain intensity, frequency and intensity of low back pain or discomfort episodes, low back pain-related disability, work-related musculoskeletal discomfort, tactile acuity, and pressure pain threshold. Mechanistic outcomes will include corticospinal excitability, somatosensory cortical responses during unstable sitting, postural control, lumbar multifidus motor-unit behavior, and lumbar multifidus contractile response.

The primary objective is to determine whether 4 weeks of active lumbar sensory stimulation produces greater improvements in clinical outcomes than a sham intervention and whether clinical changes are accompanied by changes in sensorimotor and neuromuscular outcomes.

Visão geral do estudo

Status

Ainda não está recrutando

Condições

Descrição detalhada

Phase III is a prospective, double-blind, sham-controlled randomized clinical trial designed to evaluate the clinical effectiveness and potential sensorimotor mechanisms of a wearable sensory stimulation belt in office workers with chronic nonspecific low back pain.

After eligibility screening and written informed consent, participants will undergo a baseline laboratory assessment. Baseline clinical assessments will include pain intensity, low back pain-related disability, work-related musculoskeletal discomfort, movement-control testing, tactile acuity, and pressure pain threshold.

Baseline mechanistic assessments will characterize corticospinal, cortical, postural, motor-unit, and lumbar multifidus function. Corticospinal excitability will be assessed using single-pulse transcranial magnetic stimulation (TMS), with motor-evoked potentials recorded from the lumbar multifidus and erector spinae muscles. Somatosensory cortical and postural responses will be assessed during unstable sitting using functional near-infrared spectroscopy (fNIRS) over the bilateral primary somatosensory cortex together with inertial measurement units (IMUs). Participants will also perform a repeated loaded forward-bending task while lumbar multifidus motor-unit behavior is recorded using decomposition electromyography (dEMG) and trunk movement is recorded using IMUs. Lumbar multifidus morphology and contractile response will be assessed using rehabilitative ultrasound imaging (RUSI) at rest and during contralateral arm lifting.

Following completion of the baseline assessment, participants will be randomly allocated in a 1:1 ratio to an active sensory stimulation belt group or a sham belt group using a computer-generated block randomization sequence. Allocation will be concealed using sequentially numbered, opaque, sealed envelopes prepared by a research assistant who is not involved in outcome assessment.

Participants assigned to the active intervention group will receive a sensory stimulation belt programmed with the lumbar vibration parameters identified during the preceding Phase II parameter-optimization study. Participants assigned to the sham group will receive a belt designed to have similar appearance, weight, sound, and user interface. The sham belt will provide only a brief, low-level surface vibration at the beginning of use and will subsequently cease active stimulation so that it does not provide the intended sustained sensory stimulation.

Participants and outcome assessors will be blinded to group allocation. Device programming and allocation management will be performed by research personnel who are not involved in clinical or mechanistic outcome assessment.

Participants will be instructed to wear their assigned belt during their usual office working hours for at least 4 hours per day, 5 days per week, for 4 consecutive weeks. Participants may continue their usual occupational activities while wearing the belt.

Throughout the 4-week intervention period, participants will complete a daily study logbook documenting belt-wear duration, number of wear sessions, pain intensity before and after belt use, local discomfort or skin reactions, technical or device-related problems, and reasons for missed use when applicable. A member of the research team will conduct weekly follow-up to review adherence, identify technical problems, reinforce study procedures, and document adverse events.

At the end of the 4-week intervention, participants will return to the laboratory for post-intervention assessments using procedures comparable to the baseline assessment. Clinical assessments will include pain intensity, low back pain-related disability, work-related musculoskeletal discomfort, movement-control testing, tactile acuity, and pressure pain threshold. Mechanistic assessments will include corticospinal excitability using TMS, somatosensory cortical and postural responses during unstable sitting using fNIRS and IMUs, lumbar multifidus motor-unit behavior during loaded forward bending using dEMG, and lumbar multifidus contractile response using RUSI.

The primary efficacy analysis will compare changes in clinical outcomes between the active and sham groups over the 4-week intervention period. Linear mixed-effects models will be used to evaluate group, time, and group-by-time interaction effects for continuous outcomes. Repeated daily pain or discomfort measurements will also be evaluated using mixed-effects models. The frequency of pain or discomfort episodes may be analyzed using Poisson or negative-binomial regression, depending on the distribution of the data.

The primary analysis will follow the intention-to-treat principle. A complementary per-protocol analysis will be performed for participants who complete at least 75% of the prescribed belt use. Treatment effects will be reported with 95% confidence intervals.

Safety, adherence, comfort, usability, and device-related problems will be monitored throughout the intervention. Belt use will be discontinued if a participant requests discontinuation, develops clinically important symptom aggravation, experiences a significant adverse event, or develops a device-related problem that makes continued use inappropriate.

Tipo de estudo

Intervencional

Inscrição (Estimado)

72

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

  • Nome: Apinkarn Jaroenlarp, PhD Candidate
  • Número de telefone: +66-89-329-6194
  • E-mail: j.apinkarn@hotmail.com

Locais de estudo

    • Changwat Nakhon Pathom
      • Salaya, Changwat Nakhon Pathom, Tailândia, 73170
        • Faculty of Physical Therapy, Mahidol University
        • Contato:
        • Contato:
        • Investigador principal:
          • Peemongkon Wattananon, PhD
        • Subinvestigador:
          • Apinkarn Jaroenlarp, PhD Candidate
        • Subinvestigador:
          • Preeyajit Anukulpipat, BSc
        • Subinvestigador:
          • Nguyen The Minh Hung, BSc
        • Subinvestigador:
          • Kent Fhilip Aseron, BSc

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  1. Office workers who currently sit for at least 6 hours per workday.
  2. Age between 20 and 60 years.
  3. Chronic nonspecific low back pain for at least 3 months.
  4. Current pain intensity of at least 2/10 on the Numeric Pain Rating Scale.

Exclusion Criteria:

  1. History of seizure in the participant or a family member.
  2. Implanted pacemaker.
  3. Contraindications to TMS or fNIRS, including relevant open wound, infection, skin lesion, or other condition preventing safe measurement.
  4. Acute cerebral hemorrhage.
  5. History of major spinal surgery, fracture, or traumatic injury to the lumbar spine.
  6. Evidence of neurological deficits, including radiculopathy, loss of sensation, or motor weakness in the lower limbs.
  7. Diagnosis of a systemic inflammatory condition, including ankylosing spondylitis or rheumatoid arthritis.
  8. Allergy to adhesives or history of severe skin sensitivity to vibration or mechanical pressure.
  9. Body mass index greater than 30 kg/m2 because of potential effects on RUSI, dEMG, and fNIRS signal quality.
  10. Pregnancy.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Active Sensory Stimulation Belt
Participants will receive an active sensory stimulation belt programmed using the optimized lumbar vibration parameters identified during Phase II. Participants will wear the belt during usual office work for at least 4 hours per day, 5 days per week, for 4 weeks.
The active sensory stimulation belt is a wearable device designed to deliver controlled mechanical sensory stimulation to the lumbar region during prolonged office work. The belt will be programmed using the optimized vibration parameters identified during the preceding Phase II neurophysiological optimization study. Participants will wear the active belt during usual office work for at least 4 hours per day, 5 days per week, for 4 weeks.
Comparador Falso: Sham Sensory Stimulation Belt
Participants will receive a sham belt designed to resemble the active belt in appearance, weight, sound, and user interface. The sham device will provide a brief, low-level surface vibration at the beginning of use and will subsequently cease active stimulation. Participants will wear the sham belt during usual office work for at least 4 hours per day, 5 days per week, for 4 weeks.
The sham sensory stimulation belt is designed to resemble the active belt in appearance, weight, sound, and user interface. The sham device will provide a brief, low-level surface vibration at the beginning of use and will subsequently cease active stimulation. It will therefore not provide the sustained lumbar sensory stimulation delivered by the active device. Participants will wear the sham belt during usual office work for at least 4 hours per day, 5 days per week, for 4 weeks.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in low back pain intensity
Prazo: Baseline and 4 weeks
Pain intensity will be measured using the 11-point Numeric Pain Rating Scale (NPRS), ranging from 0 (no pain) to 10 (worst imaginable pain). Current pain and average pain during the previous 7 days will be recorded. Change in pain intensity from baseline to the end of the 4-week intervention will be compared between the active and sham groups.
Baseline and 4 weeks
Frequency of low back pain or discomfort episodes
Prazo: Daily during the 4-week intervention
Participants will record the occurrence of low back pain or discomfort episodes in a daily study logbook throughout the 4-week intervention. The number of episodes will be summarized over the intervention period and compared between the active and sham groups.
Daily during the 4-week intervention
Daily change in low back pain intensity associated with belt use
Prazo: Before and after belt use on each study day for 4 weeks
Participants will rate low back pain intensity using the 0-10 Numeric Pain Rating Scale immediately before the first belt-wear period and after the final belt-wear period of each study day. Repeated daily pain responses will be compared between the active and sham groups.
Before and after belt use on each study day for 4 weeks
Change in low back pain-related disability
Prazo: Baseline and 4 weeks
Low back pain-related disability will be assessed using the Oswestry Disability Index (ODI). The questionnaire score is expressed as a percentage, with higher scores indicating greater disability. Change from baseline to 4 weeks will be compared between groups.
Baseline and 4 weeks
Change in work-related musculoskeletal discomfort
Prazo: Baseline and 4 weeks
Work-related musculoskeletal discomfort will be assessed using the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ), which evaluates the frequency, severity, and interference with work associated with musculoskeletal discomfort during the previous working week. The lower-back score and total CMDQ score will be analyzed.
Baseline and 4 weeks
Change in lumbar tactile acuity
Prazo: Baseline and 4 weeks
Lumbar tactile acuity will be assessed using a three-point aesthesiometer to determine two-point discrimination threshold over the lumbar region. Lower discrimination thresholds indicate greater tactile spatial acuity.
Baseline and 4 weeks
Change in pressure pain threshold
Prazo: Baseline and 4 weeks
Pressure pain threshold will be measured using a digital pressure algometer at predefined local lumbar and remote anatomical sites. Pressure will be gradually increased until the participant first reports pain. Change in pressure pain threshold from baseline to 4 weeks will be compared between groups.
Baseline and 4 weeks

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change in lumbar multifidus and erector spinae motor-evoked potential amplitude
Prazo: Baseline and 4 weeks
Corticospinal excitability of the lumbar multifidus will be assessed using single-pulse transcranial magnetic stimulation with surface electromyographic recording. Motor-evoked potential amplitude will be quantified as peak-to-peak amplitude in millivolts.
Baseline and 4 weeks
Change in active motor threshold of lumbar multifidus and erector spinae measured by transcranial magnetic stimulation
Prazo: Baseline and 4 weeks
Active motor threshold of lumbar multifidus and erector spinae will be determined during standardized submaximal contraction and expressed as a percentage of maximum stimulator output.
Baseline and 4 weeks
Change in motor-evoked potential latency of lumbar multifidus and erector spinae
Prazo: Baseline and 4 weeks
Motor-evoked potential latency of lumbar multifidus and erector spinae will be measured as the time in milliseconds from the transcranial magnetic stimulation pulse to the onset of the electromyographic motor-evoked potential.
Baseline and 4 weeks
Change in cortical motor map volume of lumbar multifidus and erector spinae
Prazo: Baseline and 4 weeks
Cortical motor map volume of lumbar multifidus and erector spinae will be derived from motor-evoked potential amplitudes recorded across the standardized transcranial magnetic stimulation scalp grid.
Baseline and 4 weeks
Change in cortical motor map area of lumbar multifidus and erector spinae
Prazo: Baseline and 4 weeks
Cortical motor map area of lumbar multifidus and erector spinae will be calculated from the number and spatial distribution of responsive stimulation sites within the standardized transcranial magnetic stimulation grid.
Baseline and 4 weeks
Change in oxygenated hemoglobin concentration in the bilateral primary somatosensory cortex during unstable sitting
Prazo: Baseline and 4 weeks
Oxygenated hemoglobin concentration will be recorded from the bilateral primary somatosensory cortex using functional near-infrared spectroscopy during unstable sitting. The primary fNIRS metric will be the baseline-corrected change in oxygenated hemoglobin concentration during the unstable sitting condition.
Baseline and 4 weeks
Change in deoxygenated hemoglobin concentration in the bilateral primary somatosensory cortex during unstable sitting
Prazo: Baseline and 4 weeks
Deoxygenated hemoglobin concentration will be recorded from the bilateral primary somatosensory cortex using functional near-infrared spectroscopy during unstable sitting.
Baseline and 4 weeks
Change in total hemoglobin concentration in the bilateral primary somatosensory cortex during unstable sitting
Prazo: Baseline and 4 weeks
Total hemoglobin concentration will be calculated from oxygenated and deoxygenated hemoglobin signals recorded using functional near-infrared spectroscopy during unstable sitting.
Baseline and 4 weeks
Change in lumbar resultant angular velocity during unstable sitting
Prazo: Baseline and 4 weeks
Inertial measurement units positioned over the lumbar and pelvic regions will record trunk movement during unstable sitting. Resultant angular velocity will be calculated in degrees per second as a quantitative measure of postural-control behavior.
Baseline and 4 weeks
Change in number of lumbar multifidus motor units during loaded forward bending
Prazo: Baseline and 4 weeks
Decomposition electromyography will be used to identify lumbar multifidus motor units during repeated 45-degree trunk flexion-extension while holding 5% of body weight. The number of motor units meeting predefined decomposition quality criteria will be recorded.
Baseline and 4 weeks
Change in lumbar multifidus motor-unit action-potential amplitude during loaded forward bending
Prazo: Baseline and 4 weeks
Lumbar multifidus motor-unit action-potential amplitude will be derived from decomposition electromyography during the loaded forward-bending task and expressed in microvolts.
Baseline and 4 weeks
Change in lumbar multifidus motor-unit firing rate during loaded forward bending
Prazo: Baseline and 4 weeks
Lumbar multifidus motor-unit firing rate will be quantified using decomposition electromyography during repeated loaded forward bending and expressed in pulses per second.
Baseline and 4 weeks
Change in lumbar multifidus percentage thickness change during contraction
Prazo: Baseline and 4 weeks
Lumbar multifidus thickness will be measured using B-mode rehabilitative ultrasound imaging at the L4-L5 level at rest and during contralateral arm lifting against standardized resistance. Percentage thickness change will be calculated as [(contracted thickness - resting thickness) / resting thickness] × 100 and used as an estimate of lumbar multifidus contractile response.
Baseline and 4 weeks
Change in lumbar multifidus absolute thickness change during contraction
Prazo: Baseline and 4 weeks
Absolute lumbar multifidus thickness change will be calculated as contracted thickness minus resting thickness using rehabilitative ultrasound imaging at the L4-L5 level.
Baseline and 4 weeks
Belt-wear adherence
Prazo: Daily throughout the 4-week intervention
Adherence will be determined from the participant daily logbook using recorded belt-wear duration and frequency. The prescribed use is at least 4 hours per day, 5 days per week, for 4 weeks. Adherence will be summarized as the number and percentage of prescribed study days completed and the proportion of prescribed belt-wear time completed.
Daily throughout the 4-week intervention
Number of participants with device-related adverse events
Prazo: Throughout the 4-week intervention
Device-related adverse events will include increased low back pain, local discomfort, skin redness or irritation, excessive warmth, numbness, dizziness, or other symptoms judged to be related to use of the study belt. Events will be recorded in the participant daily logbook and reviewed during weekly follow-up contacts. The number of participants experiencing at least one device-related adverse event will be reported for each group.
Throughout the 4-week intervention

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Investigador principal: Peemongkon Wattananon, PhD, Mahidol university

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de janeiro de 2028

Conclusão Primária (Estimado)

31 de dezembro de 2028

Conclusão do estudo (Estimado)

31 de dezembro de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

26 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

30 de agosto de 2026

Primeira postagem (Real)

3 de setembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

3 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

30 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

De-identified individual participant data that underlie the results reported in publications from this trial may be shared with qualified researchers upon reasonable request. Shared data may include de-identified clinical outcomes, adherence data, and processed mechanistic outcome data. Direct identifiers and information that could reasonably permit participant re-identification will not be shared. Data sharing will be subject to approval by the principal investigator and applicable Mahidol University and ethics requirements, and may require a data-use agreement.

Prazo de Compartilhamento de IPD

Data will become available beginning 6 months after publication of the primary trial results and will remain available for 5 years after publication.

Critérios de acesso de compartilhamento IPD

Qualified researchers may request access by submitting a written proposal to the principal investigator describing the research question, requested variables, analysis plan, and intended use of the data. Requests will be reviewed for scientific merit, ethical appropriateness, participant confidentiality, and compatibility with the original informed consent. Approved requests may require execution of a data-use agreement before de-identified data are provided.

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever