Viewing Study NCT05213845



Ignite Creation Date: 2024-05-06 @ 5:09 PM
Last Modification Date: 2024-10-26 @ 2:23 PM
Study NCT ID: NCT05213845
Status: TERMINATED
Last Update Posted: 2023-01-25
First Post: 2022-01-17

Brief Title: Spine Rehabilitation Using Spine Flexion Extension Full Active Range of Motion for Patients With Chronic Low Back Pain
Sponsor: Groupe Hospitalier de la Region de Mulhouse et Sud Alsace
Organization: Groupe Hospitalier de la Region de Mulhouse et Sud Alsace

Study Overview

Official Title: Assessment of Spine Rehabilitation Program Using Spine Flexion and Extension Full Active Range of Motion for Patients With Chronic Low Back Pain a Monocentric Prospective Cohort Study
Status: TERMINATED
Status Verified Date: 2022-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: insufficient recruitment to meet the objectives in time
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: REACTIVE
Brief Summary: 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
Detailed Description: 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

pain intensity
kinesiophobia
active range of motion of lumbar flexion and lumbar extension

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

Visual Analogue Pain Scale
Fear Avoidance Beliefs Questionnaire FABQ
Double-inclinometer to measure active range of motion of lumbar flexion and lumbar extension

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2021-A02319-32 OTHER ANSM None