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Fear-Avoidance Beliefs and Physical Function in Patients With Lumbar Disc Herniation (FAB-LDH)

10 de agosto de 2026 atualizado por: Mohammed Issa, Istinye University

The Relationship Between Fear-Avoidance Beliefs and Trunk Muscle Endurance, Balance, and Functional Impairment in Patients With Lumbar Disc Herniation

Lumbar disc herniation is one of the most common causes of low back pain and is associated with substantial functional limitations and reduced quality of life, particularly among working-age individuals. Displacement of disc material toward the spinal canal may result in mechanical compression and inflammation of the nerve roots, leading to pain, restricted movement, and reduced functional performance.

The course of low back pain cannot be explained solely by biomechanical and anatomical factors. Psychosocial factors also play an important role in symptom persistence and functional outcomes. Within this context, the fear-avoidance model provides an important theoretical framework, suggesting that individuals may develop fear of movement and avoid physical activities because they believe these activities may increase pain or cause further injury. Over time, avoidance behaviors may contribute to physical deconditioning, reduced muscle function, and increased functional impairment.

The Fear-Avoidance Beliefs Questionnaire is commonly used to assess individuals' beliefs regarding the relationship between pain, physical activity, and work-related activities. Higher levels of fear-avoidance beliefs have been associated with greater pain severity, increased disability, and poorer physical performance in individuals with low back pain.

Trunk muscle endurance plays a key role in maintaining spinal stability. Adequate endurance of the paraspinal and abdominal muscles supports mechanical stability of the spine and contributes to the safe performance of functional movements. The Biering-Sørensen Test and plank test are commonly used to assess trunk muscle endurance in clinical and research settings. The Biering-Sørensen Test evaluates the endurance of the trunk extensor muscles, whereas plank-based tests assess the endurance of the anterior and lateral trunk musculature.

Functional impairment in individuals with low back pain can be evaluated using the Oswestry Disability Index, a self-reported questionnaire that assesses limitations experienced during activities of daily living. Functional mobility and performance may also be evaluated using the Timed Up and Go test, which involves standing up from a chair, walking a short distance, turning, returning to the chair, and sitting down. This test reflects mobility, dynamic balance, and functional performance during daily activities.

Postural control and balance may also be affected in individuals with low back pain. Reduced static balance performance can negatively influence functional activities and mobility. The Single-Leg Stance Test is a practical clinical measure used to assess postural stability and static balance.

Although previous studies have examined associations between psychosocial factors and functional status in individuals with low back pain, studies evaluating the relationship between fear-avoidance beliefs, trunk muscle endurance, balance, and functional performance together remain limited. Identifying these relationships may contribute to the development of more comprehensive rehabilitation programs for individuals with lumbar disc herniation.

Visão geral do estudo

Status

Recrutamento

Condições

Tipo de estudo

Observacional

Inscrição (Estimado)

65

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

Locais de estudo

      • Istanbul, Turquia (Türkiye), 34010
        • Recrutamento
        • Istinye University
        • Contato:
        • Subinvestigador:
          • Kubra Kardes, Asst. Prof.

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
  • Adulto mais velho

Aceita Voluntários Saudáveis

N/D

Método de amostragem

Amostra de Probabilidade

População do estudo

The study will include volunteer individuals aged 18-65 who applied to a physiotherapy and rehabilitation clinic and were diagnosed with lumbar disc herniation.

Descrição

Inclusion Criteria:

  • Aged between 18 and 65 years
  • Clinically and/or radiologically diagnosed with lumbar disc herniation
  • Presence of low back pain for at least 3 months
  • Sufficient cognitive capacity to understand and perform the assessment procedures
  • Ability to walk independently
  • Willingness to participate voluntarily and provide written informed consent

Exclusion Criteria:

  • History of lumbar spine surgery
  • History of neurological disorders, such as stroke or Parkinson's disease
  • Vestibular disorders or severe balance impairment
  • History of orthopedic injury or surgery affecting the lower extremities
  • Presence of rheumatological disease
  • Pregnancy
  • Severe pain or an acute inflammatory condition that prevents completion of the assessment procedures

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

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Fear-Avoidance Beliefs
Prazo: 4 weeks
Fear-avoidance beliefs related to pain will be assessed using the Fear-Avoidance Beliefs Questionnaire. The Fear-Avoidance Beliefs Questionnaire is a self-reported questionnaire that evaluates individuals' fear-avoidance beliefs regarding pain in relation to physical activity and work-related activities. The questionnaire consists of 16 items and includes two subscales: the Physical Activity subscale and the Work subscale. Participants rate each statement on a Likert-type scale ranging from 0 (completely disagree) to 6 (completely agree). Higher scores indicate stronger fear-avoidance beliefs, suggesting greater concern that physical activity or work-related activities may worsen pain or cause further injury. Lower scores indicate fewer fear-avoidance beliefs and less perceived threat associated with movement and activity.
4 weeks
Lumbar Extensor Muscle Endurance
Prazo: 4 weeks
Lumbar extensor muscle endurance will be assessed using the Biering-Sørensen Test. During the test, participants will be positioned prone on a treatment table, with the pelvis and lower extremities stabilized. Participants will be instructed to maintain their upper body in a horizontal position with the trunk extending beyond the edge of the table. The duration for which the participant maintains this position will be recorded in seconds using a stopwatch. The test will be terminated if the participant is unable to maintain the required position, demonstrates a loss of alignment, or wishes to stop the test. A longer holding time indicates greater lumbar extensor muscle endurance, whereas a shorter holding time indicates reduced lumbar extensor muscle endurance.
4 weeks
Abdominal Muscle Endurance
Prazo: 4 weeks
Abdominal muscle endurance will be assessed using the plank test. Participants will assume a prone plank position with the elbows positioned under the shoulders and the toes in contact with the floor. They will be instructed to maintain the trunk in a straight line. The duration for which the position is maintained will be recorded in seconds using a stopwatch. The test will be terminated if trunk alignment is lost or if the participant is unable to continue. A longer holding time indicates greater abdominal muscle endurance and trunk stabilization capacity, whereas a shorter holding time indicates reduced abdominal muscle endurance.
4 weeks
Assessment of Functional Impairment
Prazo: 4 weeks
Functional impairment in activities of daily living will be assessed using the Oswestry Disability Index. The Oswestry Disability Index is a self-reported questionnaire that evaluates the impact of low back pain on daily activities. It consists of 10 sections, each containing six response options that reflect the individual's functional status during daily activities. Each section is scored from 0 to 5, and the total score is calculated as a percentage. Higher Oswestry Disability Index scores indicate greater functional impairment and disability related to low back pain, whereas lower scores indicate less functional impairment and better functional status.
4 weeks
Assessment of Functional Performance
Prazo: 4 weeks
Functional mobility and performance will be assessed using the Timed Up and Go test. Participants will begin in a seated position in a standard chair. Upon instruction, participants will stand up, walk three meters to a designated point, turn around, walk back to the chair, and sit down. The completion time will be measured in seconds using a stopwatch. A shorter completion time indicates better functional mobility, dynamic balance, and walking performance, whereas a longer completion time indicates reduced functional mobility and performance.
4 weeks
Assessment of Balance Performance
Prazo: 4 weeks
Static balance performance will be assessed using the Single-Leg Stance Test. Participants will be instructed to stand on one leg with their arms positioned alongside the body. The duration for which they are able to maintain balance while keeping the opposite foot off the floor will be recorded in seconds using a stopwatch. The test will be terminated if the raised foot touches the floor, the stance foot changes position, or balance is lost. The test may be performed on both the right and left legs, and the holding times will be recorded separately. A longer standing time indicates better static balance and postural stability, whereas a shorter standing time indicates reduced static balance performance.
4 weeks

Colaboradores e Investigadores

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

Patrocinador

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 (Real)

30 de junho de 2026

Conclusão Primária (Estimado)

30 de setembro de 2026

Conclusão do estudo (Estimado)

30 de outubro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

23 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

23 de junho de 2026

Primeira postagem (Real)

29 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

11 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

10 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

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

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