Effect of Sciatic Nerve Mobilization on Lower Extremity Pain Perception

Официальное название

The Effect of Sciatic Nerve Mobilization on Pain Perception in Lower Extremity Peripheral Nerves

Обзор

This randomized controlled study aims to investigate the effect of sciatic nerve mobilization on pain perception in lower extremity peripheral nerves, specifically the tibial and common peroneal nerves. The study will be conducted in university students at Fenerbahçe University. Participants will be randomly assigned to either an intervention group or a control group. Pressure pain threshold (PPT) will be measured using a pressure algometer at standardized anatomical points over the tibial and common peroneal nerves before and after the intervention period. Demographic and clinical information, including age, sex, height, weight, dominant lower extremity, physical activity level, history of lower extremity injury or surgery, neurological or systemic disease, and regular medication use, will also be recorded. Participants in the intervention group will receive a standardized sciatic nerve mobilization protocol consisting of sliding-type neurodynamic mobilization performed in the supine position, including components of hip flexion, knee extension, and ankle dorsiflexion/plantarflexion in a rhythmic sequence. No intervention will be applied to the control group. The primary purpose of the study is to determine whether sciatic nerve mobilization changes pressure pain threshold values in the tibial and common peroneal nerves compared with no intervention.

Подробное описание

This randomized controlled pilot study aims to investigate the effect of sciatic nerve mobilization on pain perception in lower extremity peripheral nerves, specifically the tibial nerve and the common peroneal nerve, in healthy university students. The study will be conducted at Fenerbahçe University.

A total of 34 participants will be included. Eligible participants will be students aged 18 to 30 years at Fenerbahçe University who voluntarily agree to participate and meet the study eligibility criteria. Participants will be randomly assigned to an intervention group or a control group.

Pain perception will be assessed using pressure pain threshold measurements obtained with a pressure algometer at standardized anatomical points over the tibial and common peroneal nerves. Measurements will be performed before and after the study procedure using the same protocol for all participants.

Participants in the intervention group will receive a standardized sliding-type sciatic nerve mobilization protocol performed in the supine position. The mobilization includes coordinated movements of hip flexion, knee extension, and ankle dorsiflexion/plantarflexion to create a sliding effect on the sciatic nerve. The control group will not receive any intervention.

Вмешательства

• Другое Sciatic Nerve Mobilization
  A standardized sliding-type sciatic nerve mobilization will be applied in the supine position. The technique includes coordinated hip flexion, knee extension, and ankle dorsiflexion/plantarflexion movements to produce a sliding effect on the sciatic nerve.

Первичные конечные точки

• Pressure Pain Threshold of the Tibial Nerve [Срок оценки: Before intervention and immediately after intervention]
• Pressure Pain Threshold of the Common Peroneal Nerve [Срок оценки: Before intervention and immediately after intervention]

Критерии участия

Критерии включения

• Aged 18 to 30 years
• Being a student at Fenerbahçe University
• No history of major trauma or surgery in the lower extremity within the last 6 months
• Voluntarily agreeing to participate in the study and signing the informed consent form

Критерии исключения

• History of neurological disease
• History of lower extremity peripheral nerve injury
• Having undergone lower extremity surgery within the last 6 months
• Regular use of analgesic or muscle relaxant medications
• Pregnancy
• Presence of any systemic disease that may interfere with the assessment or intervention procedures

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Простое слепое

Основная цель

Фундаментальное исследование

Центры проведения

Turkey (Türkiye) · 1 центр

• Fenerbahçe University — Istanbul

Идентификаторы

NCT: NCT07525895 · FenerbahceUniver

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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