- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07525895
Effect of Sciatic Nerve Mobilization on Lower Extremity Pain Perception
The Effect of Sciatic Nerve Mobilization on Pain Perception in Lower Extremity Peripheral Nerves
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
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.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ataşehir
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Istanbul, Ataşehir, Turkey (Türkiye), 34758
- Fenerbahçe University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Sciatic Nerve Mobilization Group
Participants 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.
|
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.
|
|
No Intervention: Control Group
Participants 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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pressure Pain Threshold of the Tibial Nerve
Time Frame: Before intervention and immediately after intervention
|
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
Time Frame: Before intervention and immediately after intervention
|
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
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sümeyye Akçay, Asst. Prof., Fenerbahçe University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- FenerbahceUniver
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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