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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02007135
Other study ID # 2013_SBrumagne_pneumvibrators
Secondary ID
Status Completed
Phase N/A
First received December 5, 2013
Last updated October 14, 2015
Start date November 2013
Est. completion date October 2015

Study information

Verified date October 2015
Source Katholieke Universiteit Leuven
Contact n/a
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the concurrent validity of a newly developed pneumatic, fMRI compatible muscle vibrator as compared to a electromagnetic muscle vibrator in the stimulation of muscle proprioceptors.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date October 2015
Est. primary completion date November 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 45 Years
Eligibility Inclusion criteria for healthy individuals:

- Age: 20-45 years old

- No history of low back pain

- A score of 0% 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, pelvis or lower quadrant

- One of the following conditions: Parkinson, MS, Stroke with sequels....

- Radicular symptoms

- Not Dutch-speaking

- Strong opioids

- Neck pain

- Ankle problems

- Smoking

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium Katholieke Universiteit Leuven Leuven

Sponsors (2)

Lead Sponsor Collaborator
Katholieke Universiteit Leuven Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

References & Publications (1)

Claeys K, Brumagne S, Dankaerts W, Kiers H, Janssens L. Decreased variability in postural control strategies in young people with non-specific low back pain is associated with altered proprioceptive reweighting. Eur J Appl Physiol. 2011 Jan;111(1):115-23. doi: 10.1007/s00421-010-1637-x. Epub 2010 Sep 8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Proprioceptive postural control Center of pressure displacement on a 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. 6 months No
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