Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2021-A02319-32 | Other Identifier | ANSM |
Not provided
Not provided
insufficient recruitment to meet the objectives in time
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The main objective of this study is to assess efficacy of a spine rehabilitation program, using spine flexion and extension full active range of motion, on physical disability of patients with chronic low back pain.
Secondary objectives
The other objectives of this study are to assess the impact of spine rehabiliation program using spine flexion and extension full active range of motion on :
Conduct of research
After receiving the written consent of the study, participants will benefit from 5 sessions of spine flexion and extension full active range of motion exercises. The following tests and questionnaires will be performed before (baseline) and after (posttreatment) the 5 sessions :
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with chronic low back pain | Other |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Spine flexion/extension active range of motion exercises | Procedure | Five full active range of motion rehabilitation sessions will be scheduled. Four or the five following full active range of motion exercises will be performed during one rehabilitation session : spine flexion and extension (quadrupedic position), lumbar flexion and extension (sitting position), posterior and anterior pelvic tilt (sitting and standing position), lumbar flexion and extension (standing position) and Jefferson Curl exercise. All five rehabilitation sessions must be performed within 60 days |
| Measure | Description | Time Frame |
|---|---|---|
| Roland-Morris disability questionnaire | The Roland-Morris questionnaire is a 24-item self report questionnaire assessing physical disability, ranging from 0 (no disability) to 24 (severe disability). | Posttreatment (2 months) |
| Measure | Description | Time Frame |
|---|---|---|
| Pain intensity | Pain intensity will be measured with a Visual Analog Pain Scale, from 0 (no pain) to 10 (pain of maximum intensity) | Posttreatment (2 months) |
| Fear Avoidance Beliefs Questionnaire (FABQ) |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cabinet de masso-kinésithérapie | Mulhouse | 68100 | France |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
The FABQ is a patient reported questionnaire which specifically focuses on how patient's fear-avoidance beliefs about physical activity may affect and contribute to his/her low back pain and resulting disability.
| Posttreatment (2 months) |
| Active range of motion of lumbar flexion and lumbar extension | Active range of motion of lumbar flexion and lumbar extension will be measured with two inclinometers. | Posttreatment (2 months) |
| ID | Term |
|---|---|
| D017116 | Low Back Pain |
| D000092442 | Kinesiophobia |
| ID | Term |
|---|---|
| D001416 | Back Pain |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010698 | Phobic Disorders |
| D001008 | Anxiety Disorders |
| D001523 | Mental Disorders |
Not provided
Not provided