Viewing Study NCT05467592



Ignite Creation Date: 2024-05-06 @ 5:53 PM
Last Modification Date: 2024-10-26 @ 2:37 PM
Study NCT ID: NCT05467592
Status: UNKNOWN
Last Update Posted: 2022-07-20
First Post: 2022-05-16

Brief Title: Central Sensitization in Patients Seeking Outpatient Physical Therapy Services
Sponsor: University of Kansas Medical Center
Organization: University of Kansas Medical Center

Study Overview

Official Title: Central Sensitization in Patients Seeking Outpatient Physical Therapy Services
Status: UNKNOWN
Status Verified Date: 2022-07
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is an observational study to examine presence of CS in patients with knee osteoarthritis OA chronic LBP CLBP and chronic neck pain CNP seeking outpatient physical therapy PT services The study will also examine if outcomes differ between patients with CS and patients without CS symptoms with standard PT interventions
Detailed Description: Central Sensitization CS defined as augmented pain processing is common in subgroup of nearly all chronic pain conditions including fibromyalgia CLBP OA and chronic tension headache However current studies of CS are primarily limited to research settings lacking the knowledge about prevalence of CS and rehabilitation outcomes in usual clinical care

Practicing clinicians do not routinely assess for CS symptoms Without proper screening for CS and lack of knowledge of varying levels of nervous system involvement contributing to pain clinicians are unable to fully identify the depth of the mechanisms and therefore unable to fully determine the best treatment strategies This observational study addresses this gap in knowledge by screening patients for CS symptoms

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None