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Clinical Trials/NCT04123756
NCT04123756
Terminated
Not Applicable

Smerteprofiler Som Redskab Til at prædiktere Effekten af 6-8 Ugers GLA:D®-forløb Hos Patienter Med Smertefuld Slidgigt i knæene

Aalborg University1 site in 1 country12 target enrollmentOctober 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Aalborg University
Enrollment
12
Locations
1
Primary Endpoint
pain reduction
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

Pain sensitization has been associated with pain severity in people with knee osteoarthritis (KOA) and a neuropathic pain component has been identified in up to 30% of KOA patients. Mechanistic pain profiling aims to identify the underlying mechanisms in the peripheral and central nervous systems, which are associated to the clinical pain.

In addition, the mechanisms underlying the pain relieving effect of standardized exercise therapy are largely unknown, but it is hypothesized that they are linked to the patient's ability to activate the descending pain inhibitory pathways (conditioned pain modulation, CPM) in the central nervous system. Mechanistic pain profiling including CPM have been used prognostic to identify responders to treatment, but these measures as a prognostic tool for standardized exercise therapy has not been investigated.

The primary aim of this study is to investigate if mechanistic pain profiling alone or in combination with clinical pain measures before standardized exercise therapy can predict the patients' pain reduction following the exercise therapy program

Registry
clinicaltrials.gov
Start Date
October 1, 2019
End Date
December 31, 2020
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Aalborg University
Responsible Party
Principal Investigator
Principal Investigator

Kristian Kjær Petersen

Associate Professor, M.Sc., Ph.D.

Aalborg University

Eligibility Criteria

Inclusion Criteria

  • The American College of Rheumatology for clinical knee osteoarthritis (excluding radiological OA assessment)

Exclusion Criteria

  • Known factors to influence pain and pain sensitization

Outcomes

Primary Outcomes

pain reduction

Time Frame: 1-2 weeks after last exercise session

Pain measured on a numerical rating scale from 0 (no pain) to 10 (worst pain imaginable)

Study Sites (1)

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