Low Back Pain Clinical Trial
Official title:
Evaluation of the Responsiveness of the Bridge Tests in Subjects With Non-specific Subacute or Chronic Low Back Pain
This observational study aims to investigate the internal responsiveness and external responsiveness of the Bridge Tests (supine bridge test, prone bridge test, and side bridge test) in relation to pain and disability, in subjects with subacute and chronic non-specific low back pain submitted to a physical therapy program.
Time 0 (first session of the physical therapy treatment program)
The physical therapist will explain to each patient the purpose of the study and request
informed consent and data processing consent. In the informed consent form will be specified
that the study will concern some diagnostic tests and the study protocol will not influence
the physical therapy treatment strategy in any way. Only those who give their consent will be
included in the study and will fill in a booklet containing:
- socio-demographical, anthropometric and pain data;
- the Italian version of the Oswestry Disability Index (ODI-I);
- the Italian version of the 0-100 Numerical Rating Scale (NRS). Once completed, the
questionnaires will be placed in a sealed envelope and delivered to the examiner.
The physical therapist will perform the following tests, without being aware of the results
collected during the initial clinical evaluation and will record the tests results on a
pre-printed sheet, which will then be inserted in the same envelope as well.
The tests performed are (in order of execution):
- Aberrant Movements (AM) Test,
- Active Straight Leg Raise (ASLR) Test,
- Supine Bridge Test (SuBT),
- Right Side Bridge Test (RBT),
- Left Side Bridge Test (LBT),
- Prone Bridge Test (PrBT),
- Passive Lumbar Extension (PLE) Test,
- Prone Instability Test (PIT).
The envelope containing the patient's data and the results of the tests will be sent to an
independent subject, who will take care of the data collection and their insertion into the
electronic database, assigning to each patient a numerical code as the only identification
element.
The patients will be submitted to a physical therapy treatment for eight 30-minutes sessions,
once a week.
Time 1 (at the end of the last session of the physical therapy treatment)
Those who have completed the physical therapy treatment will receive a final booklet
containing the Italian version of the Oswestry Disability Index (ODI-I), the Numerical Rating
Scale (NRS) and the Global Perceived Effect (GPE) Questionnaire. Once completed, these
questionnaires will be placed in a sealed envelope and delivered to the examiner.
Without being aware of the outcome of the questionnaires contained in the final booklet, the
same tests will be repeated:
- Aberrant Movements (AM) Test,
- Active Straight Leg Raise (ASLR) Test,
- Supine Bridge Test (SuBT),
- Right Side Bridge Test (RBT),
- Left Side Bridge Test (LBT),
- Prone Bridge Test (PrBT),
- Passive Lumbar Extension (PLE) Test,
- Prone Instability Test (PIT).
Test results will be recorded on a pre-printed sheet, which will then be inserted in the same
envelope and send to the independent subject who is responsible for data collection.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03916705 -
Thoraco-Lumbar Fascia Mobility
|
N/A | |
Completed |
NCT04007302 -
Modification of the Activity of the Prefrontal Cortex by Virtual Distraction in the Lumbago
|
N/A | |
Completed |
NCT03273114 -
Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain
|
N/A | |
Recruiting |
NCT03600207 -
The Effect of Diaphragm Muscle Training on Chronic Low Back Pain
|
N/A | |
Completed |
NCT04284982 -
Periodized Resistance Training for Persistent Non-specific Low Back Pain
|
N/A | |
Recruiting |
NCT05600543 -
Evaluation of the Effect of Lumbar Belt on Spinal Mobility in Subjects With and Without Low Back Pain
|
N/A | |
Withdrawn |
NCT05410366 -
Safe Harbors in Emergency Medicine, Specific Aim 3
|
||
Completed |
NCT03673436 -
Effect of Lumbar Spinal Fusion Predicted by Physiotherapists
|
||
Completed |
NCT02546466 -
Effects of Functional Taping on Static Postural Control in Patients With Non-specific Chronic Low Back Pain
|
N/A | |
Completed |
NCT00983385 -
Evaluation of Effectiveness and Tolerability of Tapentadol Hydrochloride in Subjects With Severe Chronic Low Back Pain Taking Either WHO Step I or Step II Analgesics or no Regular Analgesics
|
Phase 3 | |
Recruiting |
NCT05156242 -
Corticospinal and Motor Behavior Responses After Physical Therapy Intervention in Patients With Chronic Low Back Pain.
|
N/A | |
Recruiting |
NCT04673773 -
MY RELIEF- Evidence Based Information to Support People Aged 55+ Years Living and Working With Persistent Low-back Pain.
|
N/A | |
Completed |
NCT06049277 -
Mulligan Technique Versus McKenzie Extension Exercise Chronic Unilateral Radicular Low Back Pain
|
N/A | |
Completed |
NCT06049251 -
ELDOA Technique Versus Lumbar SNAGS With Motor Control Exercises
|
N/A | |
Completed |
NCT04980469 -
A Study to Explore the Effect of Vitex Negundo and Zingiber Officinale on Non-specific Chronic Low Back Pain Due to Sedentary Lifestyle
|
N/A | |
Completed |
NCT04055545 -
High Intensity Interval Training VS Moderate Intensity Continuous Training in Chronic Low Back Pain Subjects
|
N/A | |
Recruiting |
NCT05552248 -
Assessment of the Safety and Performance of a Lumbar Belt
|
||
Recruiting |
NCT05944354 -
Wearable Spine Health System for Military Readiness
|
||
Completed |
NCT05801588 -
Participating in T'ai Chi to Reduce Back Pain and Improve Quality of Life
|
N/A | |
Completed |
NCT05811143 -
Examining the Effects of Dorsal Column Stimulation on Pain From Lumbar Spinal Stenosis Related to Epidural Lipomatosis.
|