Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Assessment Tactile Sensory Function (Tactile Sense)

16. juli 2026 opdateret af: 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.

Studieoversigt

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

121

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ja

Prøveudtagningsmetode

Sandsynlighedsprøve

Studiebefolkning

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.

Beskrivelse

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.

-

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Kohorter og interventioner

Gruppe / kohorte
Intervention / Behandling
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

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Tactile Sensation normative values
Tidsramme: 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.
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Gender
Tidsramme: 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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

1. juni 2022

Primær færdiggørelse (Faktiske)

15. januar 2023

Studieafslutning (Faktiske)

20. januar 2023

Datoer for studieregistrering

Først indsendt

16. juli 2026

Først indsendt, der opfyldte QC-kriterier

16. juli 2026

Først opslået (Faktiske)

21. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

21. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • IstanbulArelUniversity

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

UBESLUTET

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Tactile Sensation Values

3
Abonner