Investigation of Central Sensitization Frequency and Related Factors in Axial Spondyloarthritis Patients

CompletedOBSERVATIONAL
Enrollment

150

Participants

Timeline

Start Date

October 20, 2019

Primary Completion Date

February 14, 2020

Study Completion Date

April 18, 2020

Conditions
Axial SpondyloarthritisCentral Sensitisation
Interventions
DIAGNOSTIC_TEST

Pressure pain threshold

The PPT assessments of spine will be performed over the spinous process and 2 cm right and left side of the corresponding spinous process. The regional PPT scores will be composed from sum of all PPT values for related segments at spine. The sacroiliac PPT scores will be obtained bilaterally from four measurement points; the first point is located 1 cm medially and caudally from spina iliaca posterior superior (SIPS) and 3 more laterally, medially and cranially.The left trapezius muscle will be used to evaluate distant control point .The 1 cm2 algometer probe will be placed vertically in the each selected point and pressure will be increased with 0.1 kg/sc until the participant reporting pressure became painful. The pressure value at which the pain is first felt will be accepted as the PPT of that point.

DIAGNOSTIC_TEST

Temporal summation

TS will be evaluated over the trapezius muscle, sacroiliac joints, C7, T6, and L3 levels at spine with manuel algometer. TS scores will be calculated for each spine level as the sum of three values which measured over the spinous process and 2 cm right and left side of corresponding level. In the evaluation of TS, a pressure as much the PPT value of each point will be applied with pain pressure algometer ten times with a 1-second interstimulus interval. Patients will be asked to rate their pain using on a 0 to 10 visual analogue scale (VAS) at 0, 5, and 10 seconds. TS will be calculated by subtracting the rating at 0 seconds from the rating at 10 seconds. The point that is located 1 cm medially and caudally from SIPS was used for SI joint TS measurement on both sides.

DIAGNOSTIC_TEST

Conditioned pain modulation

First stimulus will be applied to trapezius with the pressure that induced a pain intensity of 4 point on a 10 point VAS as called a test stimulus. After that the right hand of the patient will be immersed in 70C water for 20 seconds to create a conditioning stimulus. Second test stimulus with the same intensity of first one will be applied to trapezius after the conditioning stimulus and patients will be asked to rate their pain. If the patients cannot hold their hand in the water for 20 seconds, the test stimulus will be applied immediately after the patients removed their hands out of water. The ratio between the first and second VAS values multiplied by 100 will be defined as CPM score

DIAGNOSTIC_TEST

Central Sensitization Inventory

Standardized questionnaire to determine the level of central sensitization

OTHER

Bath Ankylosing Spondylitis Disease Activity Index

Standardized questionnaire to determine the level of disease activity in AxSpa patients

OTHER

Ankylosing Spondylitis Quality of Life

Standardized questionnaire to investigate the quality of life in AxSpa patients

OTHER

Istanbul Low Back Pain Disability Index

Standardized questionnaire to investigate the disability

OTHER

Beck Depression Inventory

Standardized questionnaire to investigate the depression

OTHER

Fatigue Severity Scale

Standardized questionnaire to investigate the fatigue

OTHER

Pittsburgh Sleep Quality Index

Standardized questionnaire to investigate the sleep quality and disturbance

OTHER

Fibromyalgia Rapid Screening Tool

Standardized questionnaire to detect fibromyalgia

OTHER

Visual analogue scale

global pain score on a 0 to 10

Trial Locations (1)

34100

Feyza Nur YUCEL, Istanbul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Marmara University

OTHER