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Chronic Low-back PainLOBACOMNCT05511012

Does the Therapist's Assessment of Movement Control in Low Back Pain Patients Correspond to an Objective Kinematic Modification

A study of Chronic Low-back Pain, run by University Hospital, Brest at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Exercise-based treatment is part of the recommendations for good practice in the treatment of low back pain (acute, sub-acute and chronic). The low back pain population is heterogeneous. Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Chronic Low-back Pain
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteFrance
Study dates
15 Dec 2022to 15 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Aged more than 18 years
  • Common low back pain with medical prescription for rehabilitation
  • Signed consent
  • Be affiliated to a social security scheme
  • Be able to perform the lumbar motion control failure tests

Who cannot join

  • Body Mass Index greater than 30 (obesity)
  • Person who does not understand French
  • Pregnant woman
  • Refusal to participate
  • Volunteer under guardianship or curatorship

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • CHU de Brest

    Brest, Finistère, 29609

    Vincent CREAC'H, +33(0)298017935, vincent.creach@univ-brest.fr

    Marine BOURHIS

    Recruiting

Other trials in France

About this study

  • Exercise-based treatment is part of the recommendations for good practice in the treatment of low back pain (acute, sub-acute and chronic).
  • The low back pain population is heterogeneous. This heterogeneity would cause the positive effects of a treatment to be canceled out by the negative effects of another part of the population.
  • This polymorphism has led several authors to classify low back pain into subgroups. These subgroups constitute more homogeneous clinical pictures and would facilitate the adaptation of treatments.
  • The recommendations of the American Physical Therapy Association suggest 5 subgroups of low back pain. One of them is "low back pain with movement coordination defect". In this subgroup, Luomajoki studied the reliability of different functional tests used in clinical practice. 6 out of 10 motion control fault tests show good reliability.
  • The quantified analysis of the movement of low back pain patients would make it possible to determine the sensitivity of detecting an anomaly in the 6 lumbar movement control tests.
Read the detailed description
  • Exercise-based treatment is part of the recommendations for good practice in the treatment of low back pain (acute, sub-acute and chronic).
  • The low back pain population is heterogeneous. This heterogeneity would cause the positive effects of a treatment to be canceled out by the negative effects of another part of the population.
  • This polymorphism has led several authors to classify low back pain into subgroups. These subgroups constitute more homogeneous clinical pictures and would facilitate the adaptation of treatments.
  • The recommendations of the American Physical Therapy Association suggest 5 subgroups of low back pain. One of them is "low back pain with movement control impairment". In this subgroup, Luomajoki studied the reliability of different functional tests used in clinical practice. 6 out of 10 motion control fault tests show good reliability.
  • The quantified analysis of the movement of low back pain patients would make it possible to determine the sensitivity of detecting an anomaly in the 6 lumbar movement control tests.

LoBaCoM is a monocentric, exploratory prospective study.

The purpose is to define a kinematic (angular) threshold corresponding to an anomaly detected clinically by three therapists for each test.

Being tested
motion control fault tests
Keywords
Low back pain, Movement control, Kinematic analysis, Clinical assessment
Medical subject headings
Low Back Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • motion control fault testsOther

    Patients make 6 motion control fault tests, in the same order. Each test is performed three times

Study groups in NCT05511012
Study groupRoleWhat they receive
motion control fault testingOtherEach patient make six motion control fault tests in the same order : 1. "waiters bow" 2. "pelvic tilt" 3. "one leg stance" 4. "sitting knee extension" 5. "rocking 4 point kneeling" 6. "prone knee bend" This tests are performed three times.
Receives: Other: motion control fault tests

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Range of compensation motion : "waiters bow" test

    Lumbar flexion measured for test number 1 "waiters bow". Patients are filmed during the test. Videos are watched by three physiotherapists. They going to establish a diagnostic normal or abnormal

    Measured: Day 0

  2. Range of compensation motion : "pelvic tilt" test

    thoracic flexion measured for test number 2 "pelvic tilt". Patients are filmed during the test. Videos are watched by three physiotherapists. They going to establish a diagnostic normal or abnormal.

    Measured: Day 0

  3. Range of compensation motion : "One leg stance" test

    Pelvic shift measured for test number 3 "One leg stance ". Patients are filmed during the test. Videos are watched by three physiotherapists. They going to establish a diagnostic normal or abnormal.

    Measured: Day 0

  4. Range of compensation motion : "sitting knee extension" test

    Lumbar flexion measured for test number 4 "sitting knee extension". Patients are filmed during the test. Videos are watched by three physiotherapists. They going to establish a diagnostic normal or abnormal.

    Measured: Day 0

  5. Range of compensation motion : "rocking 4 point kneeling" test

    Lumbar flexion and extension measured for test number 5 "rocking 4 point kneeling ". Patients are filmed during the test. Videos are watched by three physiotherapists. They going to establish a diagnostic normal or abnormal.

    Measured: Day 0

  6. Range of compensation motion : "prone knee bend" test

    Lumbar extension measured for test number 6 "prone knee bend". Patients are filmed during the test. Videos are watched by three physiotherapists. They going to establish a diagnostic normal or abnormal

    Measured: Day 0

Secondary outcomes (6)
  1. Speed of execution for test 1

    It is measured with a camera. The camera can film one hundred pictures per second. Speed of execution is measured in seconds.

    Measured: Day 0

  2. Speed of execution for test 2

    It is measured with a camera. The camera can film one hundred pictures per second. Speed of execution is measured in seconds.

    Measured: Day 0

  3. Speed of execution for test 3

    It is measured with a camera. The camera can film one hundred pictures per second. Speed of execution is measured in seconds.

    Measured: Day 0

  4. Speed of execution for test 4

    It is measured with a camera. The camera can film one hundred pictures per second. Speed of execution is measured in seconds.

    Measured: Day 0

  5. Speed of execution for test 5

    It is measured with a camera. The camera can film one hundred pictures per second. Speed of execution is measured in seconds.

    Measured: Day 0

  6. Speed of execution for test 6

    It is measured with a camera. The camera can film one hundred pictures per second. Speed of execution is measured in seconds.

    Measured: Day 0

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Aug 2022
  2. Study start15 Dec 2022
  3. Primary completion15 Dec 2026 (estimated)
  4. Study completion15 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Model description
It is a prospective, monocentric, exploratory study
Masking
None (open label)
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05511012
Sponsor's protocol ID
29BRC22.0128
Acronym
LOBACOM
Status last verified
Jun 2026
First submitted
19 Aug 2022
Last updated
11 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: All collected data that underlie results in a publication

Questions about this trial

What is this clinical trial studying?

A study of Chronic Low-back Pain, run by University Hospital, Brest at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 11 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Vincent CREAC'H (+33(0)298017935, vincent.creach@univ-brest.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Range of compensation motion : "waiters bow" test (time frame: Day 0). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jun 2026.

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