Assessment Tactile Sensory Function (Tactile Sense)

July 16, 2026 updated by: Secil OZKURT, Istanbul Arel University

Assessment of Tactile Sensory Function in the Lower Extremity of Healthy Young Individuals

A total of 121 healthy volunteers (96 females, 25 males; mean age: 20,75±2,20 years) participated in this cross-sectional study conducted in the Physiotherapy and Rehabilitation Laboratory of Istanbul Arel University. Tactile sensation was assessed using the Baseline 5-piece monofilament kit in 10 specific regions of both the dominant and non-dominant lower extremities. Measurements included the tip of the hallux, medial and lateral aspects of the leg, anterior and posterior thigh, and metatarsal regions. Data were analyzed using descriptive statistics. Between-group comparisons were made using the Mann-Whitney U test. Correlations between age, body mass index (BMI), and sensation values were analyzed using Spearman's correlation coefficient.

Study Overview

Study Type

Observational

Enrollment (Actual)

121

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

8-25 years healthy young adults university students.excluded if they had a history of lower limb injuries, systemic or neurological conditions, chronic pain, or skin-related issues potentially influencing tactile sensitivity, such as burns, calluses, scars, or tattoos.

Description

Inclusion Criteria: 18-25 years healthy young adults -

Exclusion Criteria: if they had a history of lower limb injuries, systemic or neurological conditions, chronic pain, or skin-related issues potentially influencing tactile sensitivity, such as burns, calluses, scars, or tattoos.

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Young adults
The tactile sensibility of 10 predefined regions of the lower extremity was then evaluated using the Baseline brand tactile monofilament test kit, and the results were recorded. Before starting the procedure, each participant was properly positioned on an examination table first in the supine position and then in the prone position. During the assessment, the lower extremity was placed parallel to the ground. Once the participant was in a comfortable position, they were asked to close their eyes. The same examiner performed all the measurements. To minimize measurement bias, all tests were conducted by the same trained examiner under standardized environmental and procedural conditions. However, the use of a single examiner may limit inter-rater generalizability The monofilament test was applied three times to each predetermined region. Pressure was applied until the monofilament was gentlyently bent. Participants were instructed to say "yes" as soon as they perceived the stimulus, at

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Tactile Sensation normative values
Time Frame: june 2022-January 2023
The tactile sensibility of 10 predefined regions of the lower extremity was then evaluated using the Baseline brand tactile monofilament test kit, and the results were recorded. Before starting the procedure, each participant was properly positioned on an examination table first in the supine position and then in the prone position. During the assessment, the lower extremity was placed parallel to the ground. Once the participant was in a comfortable position, they were asked to close their eyes. The same examiner performed all the measurements. To minimize measurement bias, all tests were conducted by the same trained examiner under standardized environmental and procedural conditions. However, the use of a single examiner may limit inter-rater generalizability.The monofilament test was applied three times to each predetermined region. Pressure was applied until the monofilament was gentlyently bent. Participants were instructed to say "yes" as soon as they perceived the stimulus, at
june 2022-January 2023
the normative data of the monofilament test of the lower extremity in the healthy, young Turkish population.
Time Frame: 01 June 2022- 15 Jan 2023
the normative data of the monofilament test of the lower extremity in the healthy, young Turkish population.
01 June 2022- 15 Jan 2023

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Gender
Time Frame: June 2022-January 2023
The secondary outcome was to make a comparison according to gender and laterality, whether through the dominant or non-dominant sides. Before the assessment, the laboratory environment was inspected to ensure suitability.
June 2022-January 2023

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2022

Primary Completion (Actual)

January 15, 2023

Study Completion (Actual)

January 20, 2023

Study Registration Dates

First Submitted

July 16, 2026

First Submitted That Met QC Criteria

July 16, 2026

First Posted (Actual)

July 21, 2026

Study Record Updates

Last Update Posted (Actual)

July 21, 2026

Last Update Submitted That Met QC Criteria

July 16, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • IstanbulArelUniversity

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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