Central Sensitisation and Functioning in patients with Chronic Low Back Pai

Completed

• Conditions: multifactorial back pain; Nonspecific back pain; 10028302

• Registration Number: NL-OMON45648
• Lead Sponsor: Revalidatiegeneeskunde

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

Adult (18-65 years old) patients with chronic (>3 months) low back pain admitted to pain rehabilitation at UMCG Centre for Rehabilitation (CvR).
All subjects will have signed an informed consent form before they are included in this study.

Exclusion Criteria

Radicular radiation to the leg

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main study parameters each study will be the measures of sensitisation and<br /><br>functioning:<br /><br>* Sensitisation: QST, HRV, CSI<br /><br>* Functioning: Lifting capacity, aerobic capacity, accelerometry, RAND PF, PDI,<br /><br>WAI.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>N/a.</p><br>