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Motor Learning for the Lumbar Spine Using Sensor-based Postural Feedback: a Randomized Controlled Trial

Motor Learning for the Lumbar Spine Using Sensor-based Postural Feedback: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02773160
Enrollment
80
Registered
2016-05-16
Start date
2015-04-30
Completion date
2017-03-31
Last updated
2016-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Non-specific Low Back Pain

Brief summary

A large subgroup of patients with chronic non-specific low back pain have motor control impairments. During motor control exercises, different forms of external feedback can be used to support training. This randomized controlled trial will investigate the effectiveness of different forms of external feedback during the learning phase of a motor control task for the lumbar spine in healthy subjects and patients with chronic non-specific low back pain (CNSLBP). Both healthy subjects and patients with CNSLBP will be randomized into three groups: one group will receive feedback from motion sensors, one group from a mirror and one group will receive no feedback (control group). A single session intervention with measurements at baseline and immediately post-intervention will be used.

Interventions

OTHERSensor-based postural feedback

Motion tracking sensors will provide feedback to subjects during the learning phase of a motor control task

OTHERMirror feedback

Subjects will receive feedback from a mirror during the learning phase of a motor control task

OTHERControl group

Subjects will receive no feedback during the learning phase of a motor control task

Sponsors

Jessa Hospital
CollaboratorOTHER
Hasselt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Chronic non-specific low back pain * Age 18-65 * Able to understand Dutch

Exclusion criteria

* Subjects that received lumbar stabilization exercises in the past year * Spinal surgery in the past * Pregnancy * Serious underlying pathologies (e.g. multiple sclerosis, tumors,…) * Signs or symptoms of nerve root involvement * Any physical condition at the moment of testing that can interfere with activities of daily living (e.g. serious knee pain) * Known skin-allergy for tape * BMI \> 30kg/m²

Design outcomes

Primary

MeasureTime frameDescription
Change in lumbopelvic kinematics from baseline to immediately post-interventionDay 1, immediately post-interventionKinematics will be assessed using motion sensors that are mounted on the skin at the spinous processes of L1 and S1, and at the femur.

Secondary

MeasureTime frameDescription
usefulness of feedback (Numeric rating scale 0-10)Day 1, immediately post-interventionHow useful was the feedback that was provided to the subjects during the exercise trials?
Pain during the exercise trials (Numeric rating scale 0-10)Day 1, immediately post-interventionOutcome measure primarily used as possible covariate
Fear of low back pain during the exercise trials (Numeric rating scale 0-10)Day 1, immediately post-interventionOutcome measure primarily used as possible covariate
Fear of damaging the lumbar spine during the exercise trials (numeric rating scale 0-10)Day 1, immediately post-interventionOutcome measure primarily used as possible covariate
Borg-scale to measure fatigue during the exercise trialsDay 1, immediately post-interventionOutcome measure primarily used as possible covariate

Countries

Belgium

Contacts

Primary ContactThomas Matheve, drs.
Thomas.Matheve@UHasselt.be
Backup ContactAnnick Timmermans, prof. dr.
Annick.Timmermans@uhasselt.be

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026