Plantar Pressure Values in Patients With Ankylosing Spondylitis

Sponsor

Amasya University (Other)

Overall Status

Completed

CT.gov ID

NCT05731635

Collaborator

(none)

Enrollment

Actual Duration (Months)

Study Details

Study Description

Brief Summary

this study was discovered that clinical and radiological characteristics were related to plantar pressure assessments in patients with AS.

Condition or Disease	Intervention/Treatment	Phase
Device is Used for Evalution (Event)	Diagnostic Test: plantar pressure values

Detailed Description

Determine the correlation between the plantar pressure readings of AS patients and the clinical and radiological measures utilized in the monitoring of the condition.

Method: This study covered 75 participants. The quality of life was measured using ASQoL, BASMI, BASFI, and BASDAI, and demographic information was also recorded. The pedobarographic evaluations included the recording of static and dynamic plantar pressures

Study Design

Study Type:

Observational [Patient Registry]

Actual Enrollment :

75 participants

Observational Model:

Case-Only

Time Perspective:

Cross-Sectional

Official Title:

Plantar Pressure Values in Patients With Ankylosing Spondylitis and Their Relation With Clinical and Radiological Parameters

Actual Study Start Date :

Dec 1, 2011

Actual Primary Completion Date :

Dec 1, 2012

Actual Study Completion Date :

Dec 1, 2012

Outcome Measures

Primary Outcome Measures

Pedobarographic Measurements [at begining]
The cases' foot sole pressures were measured using a pedobarography device of the RsScan International brand (1m, 3D Scientific+Balance software model). This technology measures both static (when standing) and dynamic foot sole pressures (walking). The device's pressure measuring platform has an overall frame size of 1068x418x12 mm, 8192 sensors totaling 4 sensors per cm2, and a sensor area of 975x325 mm. It has a 500 Hz frequency, a 0-200 N/cm2 pressure range, a 15° to 40° C temperature range, and a 220/110 volt connecting power.

Eligibility Criteria

Criteria

Ages Eligible for Study:

N/A and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria: patients diagnosed with AS -

Exclusion Criteria: Patients with cognitive dysfunction, vision loss that would prevent walking on the pedobarography platform, history of surgery and neurological deficit in the lower extremity, and patients who could not walk independently

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Amasya University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Esra Topçu, specialist doctor (esra topcu), Amasya University

ClinicalTrials.gov Identifier:

NCT05731635

Other Study ID Numbers:

First Posted:

Feb 16, 2023

Last Update Posted:

Feb 16, 2023

Last Verified:

Feb 1, 2023

Individual Participant Data (IPD) Sharing Statement:

Undecided

Plan to Share IPD:

Undecided

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Spondylitis

Spondylitis, Ankylosing

Study Results

No Results Posted as of Feb 16, 2023