Proprioceptive Training and Low Back Pain

This study is currently recruiting participants. (see Contacts and Locations)
Verified January 2012 by Katholieke Universiteit Leuven
Sponsor:
Collaborator:
Universitaire Ziekenhuizen Leuven
Information provided by (Responsible Party):
Simon Brumagne, Katholieke Universiteit Leuven
ClinicalTrials.gov Identifier:
NCT01505595
First received: January 4, 2012
Last updated: December 4, 2013
Last verified: January 2012
  Purpose

Proprioceptive weighting changes may explain differences in postural control performance. Deficits in proprioception are found in a subgroup of patients with low back pain.

The aim of the study is to clarify whether proprioceptive training has a positive effect on proprioceptive postural control in individuals with recurrent low back pain.


Condition Intervention
Proprioceptive Training
Low Back Pain
Other: Proprioceptive training
Other: Sham proprioceptive training

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment

Resource links provided by NLM:


Further study details as provided by Katholieke Universiteit Leuven:

Primary Outcome Measures:
  • Proprioceptive postural control [ Time Frame: 12 weeks ] [ Designated as safety issue: Yes ]
    Center of pressure displacement (force plate) in standing in response to local muscle vibration on ankle and back muscles to specifically detect the role of proprioception in postural control.


Estimated Enrollment: 40
Study Start Date: January 2012
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: January 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Proprioceptive training Other: Proprioceptive training
12 weeks
Sham Comparator: Sham proprioceptive training Other: Sham proprioceptive training
Three times daily inspiratory muscle training (2x30 breaths) at an intensity of 10% Pi,max

  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria individuals with low back pain:

  • Age: 18-45 years old
  • At least 1 year of low back pain with/without referred pain in buttock/thigh
  • At least 3 episodes of disabling low back pain
  • At least a score of 20% on the Oswestry Disability Index
  • Willingness to sign the informed consent

Exclusion Criteria:

  • History of major trauma and/or major orthopedic surgery of the spine, the pelvis or the lower quadrant
  • One of the following conditions: Parkinson, multiple sclerosis, stroke, history of vestibular disorder, respiratory disease, pregnancy
  • Radicular symptoms
  • Not Dutch-speaking
  • Strong opioids
  • Neck pain
  • Smoking history
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01505595

Contacts
Contact: Lotte Janssens, PhD student 003216329082 lotte.janssens@faber.kuleuven.be
Contact: Simon Brumagne, PhD 003216329121 simon.brumagne@faber.kuleuven.be

Locations
Belgium
Katholieke Universiteit Leuven Recruiting
Leuven, Belgium, 3000
Contact: Lotte Janssens, PhD student    003216329082    lotte.janssens@faber.kuleuven.be   
Contact: Simon Brumagne, PhD    003216329121    simon.brumagne@faber.kuleuven.be   
Sub-Investigator: Lotte Janssens, PhD student         
Principal Investigator: Simon Brumagne, PhD         
Principal Investigator: Thierry Troosters, PhD         
Sponsors and Collaborators
Katholieke Universiteit Leuven
Universitaire Ziekenhuizen Leuven
Investigators
Principal Investigator: Simon Brumagne, PhD Katholieke Universiteit Leuven
Principal Investigator: Thierry Troosters, PhD Katholieke Universiteit Leuven
Principal Investigator: Roeland Lysens, MD, PhD Katholieke Universiteit Leuven
Principal Investigator: Peter Van Wambeke, MD Universitaire Ziekenhuizen Leuven
  More Information

Publications:
Responsible Party: Simon Brumagne, Prof. dr. Simon Brumagne, Katholieke Universiteit Leuven
ClinicalTrials.gov Identifier: NCT01505595     History of Changes
Other Study ID Numbers: 2012_SBrumagne_PT-LBP, 1.5.104.03, G.0674.09
Study First Received: January 4, 2012
Last Updated: December 4, 2013
Health Authority: Belgium: Ethics Committee

Additional relevant MeSH terms:
Back Pain
Low Back Pain
Nervous System Diseases
Neurologic Manifestations
Pain
Signs and Symptoms

ClinicalTrials.gov processed this record on October 21, 2014