NCT07525895

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

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
34

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 20, 2026

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

April 6, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 13, 2026

Completed
18 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2026

Completed
Last Updated

April 27, 2026

Status Verified

April 1, 2026

Enrollment Period

1 month

First QC Date

April 6, 2026

Last Update Submit

April 24, 2026

Conditions

Keywords

Sciatic nerve mobilizationPressure pain thresholdNeurodynamic mobilizationPeripheral nerve mechanosensitivity

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

EXPERIMENTAL

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.

Other: Sciatic Nerve Mobilization

Control Group

NO INTERVENTION

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.

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.

Sciatic Nerve Mobilization Group

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

Study Officials

  • Sümeyye Akçay, Asst. Prof.

    Fenerbahçe University

    PRINCIPAL INVESTIGATOR

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
Model Details: Participants will be randomly assigned to one of two parallel groups: an intervention group receiving sciatic nerve mobilization or a control group receiving no intervention. Pressure pain threshold measurements of the tibial and common peroneal nerves will be obtained before and after the study procedure in both groups.
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.

Locations