Validation of the French Version of the Fremantle Back Awareness Questionnaire (FreBAQ) in Patients With Chronic Low Back Pain

Centre Hospitalier Universitaire de Nīmes

Status: Completed

Conditions: Low Back Pain

Treatments: Other: Pain Questionnaire

Study type: Observational

Funder types: Other

Identifiers

NCT04931758

2021-A00373-38 (Other Identifier)

NIMAO/2020-2/AH-1

Details and patient eligibility

About

In patients with chronic low back pain, the Fremantle Back Awareness Questionnaire (FreBAQ) measures the duration and intensity of pain and functional limitations. The FreBAQ is a simple tool created to assess disturbances in the body representation of the back, and the only one existing in chronic low back pain. It is a 9-item self-questionnaire in which each item is measured on a 5-point Likert scale ranging from "Never (score of 0)" to "Always (score of 4)". It assesses neglect, perceived body image of the back, accuracy in proprioceptive perception of back movements.

The psychometric properties of the FreBAQ in English, Japanese, Dutch, Turkish and German are validated and acceptable; however, they have never been studied in French and no validated version of this questionnaire in French exists.

The study investigators hypothesize that the French version of the FreBAQ has good psychometric qualities, allowing it to be used in the French chronic low back pain population.

Enrollment: 150 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Subject with no history of chronic low back pain and with a lumbar VAS <2 for more than 3 months.
• Patient with chronic low back pain: pain localized between the edge of the last lower ribs and the intergluteal groove (17) for more than 3 months.
• Patient with a lumbar VAS > 2 for more than 3 months.
• Patient whose low back pain is of common origin (no underlying organic etiology).
• In case of lumbar-radicular pain, patient with a VAS (lumbar) > VAS (leg)
• Patient who speaks and understands French
• Patient with no history of arthrodesis or lumbar disc prosthesis
• Subject affiliated or beneficiary of a health insurance plan.
• The patient must have given their free and informed consent and signed the consent form

Exclusion criteria

• It is impossible to give the subject informed information
• The patient is under safeguard of justice or state guardianship
• Patient pregnant, parturient or breastfeeding

Trial design

150 participants in 2 patient groups

Patients with low back pain

Treatment:

Other: Pain Questionnaire

Controls

Treatment:

Other: Pain Questionnaire