Ignite Creation Date:
2024-05-06 @ 7:35 PM
Last Modification Date:
2024-10-26 @ 3:10 PM
Study NCT ID:
NCT06069388
Status:
RECRUITING
Last Update Posted:
2024-05-08
First Post:
2023-09-18
Brief Title:
Effectiveness of Diaphragm Treatment in Reducing Low Back Pain
Sponsor:
University of Seville
Organization:
University of Seville
Study Overview
Official Title:
Benefits of Diaphragm Treatment in Reducing Low Back Pain in Patients With Mechanical Lumbar Pain
Status:
RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Objective Determine the benefits of including a Stretching technique of the anterior part of the diaphragm in the supine position in the conventional physiotherapy treatment protocol applied to insurance company patients with mechanical low back pain
design The aim is to carry out an experimental analytical prospective longitudinal randomized single-blind study with a blinded evaluator with an experimental group EG to which a manual technique on the diaphragm will be included in the conventional physiotherapy treatment manual therapy and electrotherapy and a control group CG to which only conventional physiotherapy treatment is administered
Subject Patient diagnosed with subacute or chronic mechanical low back pain by a specialist doctor and who has attended in Fisioclinic physiotherapy clinic Older than 18 years-old Indistinct sex Diaphragm dysfunction
Methods it is proposed to carry out a study in which two groups of subjects with mechanical low back pain will be compared One group will receive conventional physiotherapy with electrotherapy and massage therapy while the other group will receive the same conventional physiotherapy plus a specific technique aimed at the diaphragm muscle Ten treatment sessions will be carried out daily from Monday to Friday Different variables will be evaluated using scientifically validated methods such as manual diagnostic tests for lumbar mobility algometry to measure muscle pain cirtometry to evaluate chest mobility validated questionnaires for quality of life and spirometry to measure respiratory parameters These variables will be measured before and after each treatment session and later a week a month and four months after the last intervention
design The aim is to carry out an experimental analytical prospective longitudinal randomized single-blind study with a blinded evaluator with an experimental group EG to which a manual technique on the diaphragm will be included in the conventional physiotherapy treatment manual therapy and electrotherapy and a control group CG to which only conventional physiotherapy treatment is administered
Subject Patient diagnosed with subacute or chronic mechanical low back pain by a specialist doctor and who has attended in Fisioclinic physiotherapy clinic Older than 18 years-old Indistinct sex Diaphragm dysfunction
Methods it is proposed to carry out a study in which two groups of subjects with mechanical low back pain will be compared One group will receive conventional physiotherapy with electrotherapy and massage therapy while the other group will receive the same conventional physiotherapy plus a specific technique aimed at the diaphragm muscle Ten treatment sessions will be carried out daily from Monday to Friday Different variables will be evaluated using scientifically validated methods such as manual diagnostic tests for lumbar mobility algometry to measure muscle pain cirtometry to evaluate chest mobility validated questionnaires for quality of life and spirometry to measure respiratory parameters These variables will be measured before and after each treatment session and later a week a month and four months after the last intervention
Detailed Description:
None
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