The Effect of a Developed Perioperative Rehabilitation Pathway Following Lumbar Arthrodesis

NCT03427099 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2024-01-03

No results posted yet for this study

Summary

To compare the current rehabilitation pathway with the implementation of a newly developed rehabilitation pathway for patients with a single and double level lumbar arthrodesis.

Conditions

  • Physical Disability
  • Low Back Pain, Recurrent
  • Surgery

Interventions

BEHAVIORAL

Rehabilitation with a biopsychosocial focus

Rehabilitation with a biopsychosocial focus

BEHAVIORAL

Control group

usual care

Sponsors & Collaborators

  • KU Leuven

    collaborator OTHER
  • UHasselt

    collaborator UNKNOWN
  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Principal Investigators

  • Bart Depreitere, PhD, MD · Universitaire Ziekenhuizen KU Leuven

  • Thijs Swinnen, MSc, PT · Universitaire Ziekenhuizen KU Leuven

  • Tinne Thys, MSc, PT · Universitaire Ziekenhuizen KU Leuven

  • Wim Dankaerts, PhD, PT · KU Leuven

  • Simon Brumagne, PhD, PT · KU Leuven

  • Peter Van Wambeke, MD · Universitaire Ziekenhuizen KU Leuven

  • Lieven Moke, PhD, MD · Universitaire Ziekenhuizen KU Leuven

  • Sebastiaan Schelfaut, MD · Universitaire Ziekenhuizen KU Leuven

  • Ann Spriet, MSc, PT · Universitaire Ziekenhuizen KU Leuven

  • Lotte Janssens, PhD, PT · Hasselt University

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-03
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03427099 on ClinicalTrials.gov