Effect of Sciatic Nerve Mobilization on Lower Extremity Pain Perception
The Effect of Sciatic Nerve Mobilization on Pain Perception in Lower Extremity Peripheral Nerves
1 other identifier
interventional
34
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 20, 2026
CompletedFirst Submitted
Initial submission to the registry
April 6, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedApril 27, 2026
April 1, 2026
1 month
April 6, 2026
April 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pressure Pain Threshold of the Tibial Nerve
Pressure pain threshold of the tibial nerve will be assessed using a pressure algometer at a standardized anatomical point in the popliteal fossa. The algometer probe will be placed perpendicular to the skin, and pressure will be gradually increased until the participant first reports pain. The recorded value will be used as the pressure pain threshold.
Before intervention and immediately after intervention
Pressure Pain Threshold of the Common Peroneal Nerve
Pressure pain threshold of the common peroneal nerve will be assessed using a pressure algometer at a standardized anatomical point around the fibular head/neck region. The algometer probe will be placed perpendicular to the skin, and pressure will be gradually increased until the participant first reports pain. The recorded value will be used as the pressure pain threshold.
Before intervention and immediately after intervention
Study Arms (2)
Sciatic Nerve Mobilization Group
EXPERIMENTALParticipants in this group will receive a standardized sliding-type sciatic nerve mobilization. Pressure pain threshold of the tibial and common peroneal nerves will be measured before and after the intervention.
Control Group
NO INTERVENTIONParticipants in this group will receive no intervention. Pressure pain threshold of the tibial and common peroneal nerves will be measured before and after the study procedure.
Interventions
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Fenerbahçe University
Istanbul, Ataşehir, 34758, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Sümeyye Akçay, Asst. Prof.
Fenerbahçe University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The outcome assessor measuring pressure pain threshold values will be blinded to group allocation. The investigator delivering the intervention and the participants will not be blinded.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst. Prof.
Study Record Dates
First Submitted
April 6, 2026
First Posted
April 13, 2026
Study Start
March 20, 2026
Primary Completion
May 1, 2026
Study Completion
May 1, 2026
Last Updated
April 27, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be shared because the study involves a small sample from a single university population, and data sharing could increase the risk of participant identification.