Changing Trunk Muscle Activation in Patients With Recurrent Low Back Pain in Remission

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity Ghent

About this trial

The first aim of the study is to investigate the effects of a single therapy session on trunk muscle activation and lumbopelvic sensorimotor control in persons with recurrent low back pain in remission.

The second aim of the study is to examine the convergent validity of (in)voluntary multifidus activation by means of inspection and palpation during two clinically assessed lumbopelvic sensorimotor control tests in persons with recurrent low back pain in remission. The convergent validity will be examined by calculating the relationship between (1) the clinical score of (in)voluntary multifidus activation, (2) back muscle activation during the same tests measured simultaneously with electromyography and (3) trunk muscle activation during other functional movements measured with electromyography.

The third aim of the study is to investigate the convergent validity of a left-right discrimination test by calculating the relationship between (1) the left-right discrimination test, (2) position-reposition test, (3) the Fremantle Back Awareness Questionnaire and (4) the Photograph Series of Daily Activities Scale.

Eligibility criteria

Qualifiers

People between 18-65 years old

At least 2 episodes of LBP/year, with an 'episode' implying pain lasting a minimum of 24 hours which is preceded and followed by at least 1 month without LBP

Minimum LBP intensity during episodes should be ≥2/10 on a numeric rating scale (NRS) from 0 to 10

During remission the NRS intensity for LBP should be 0-1/10.

Disqualifiers

People <18 years old or >65 years old

Having any other type of non-specific LBP (acute, subacute, chronic).

Having an active extension movement pattern

Having any type of blood clotting disorder

Trial design

Treatments tested in this trial

  • Specific sensorimotor control training
  • Aspecific extension training
  • Fascia training

Treatment groups

55 Participants
are divided into 3 treatment groups

Sponsors and collaborators

University Ghent

Lead sponsor

VZW Educatieve Lichaamsbeweging

Collaborator