- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07570641
Effects of Combined Ciaphragmatic Breathing and Trunk Stabilization in Chronic Low Back Pain
May 6, 2026 updated by: lee kyoungju
The Effects of Combined Diaphragmatic Breathing and Trunk Stabilization Exercises on Pain, Function and Muscle Activity in Patients With Chronic Low Back Pain
The purpose of this study was to investigate the effects of combined diaphragmatic breathing and trunk stabilization exercises on pain, function, and muscle activity in patients with chronic low back pain, and to compare its clinical effectiveness with trunk stabilization exercise alone.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Seoul, South Korea
- Private exercise facility
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Individuals with low back pain lasting at least 3 months (12 weeks)
- Individuals with a pain intensity of 3 or higher on the Visual Analogue Scale (VAS)
- Individuals who are physically capable of performing trunk stabilization and diaphragmatic breathing exercises
Exclusion Criteria:
- Individuals with neurological or musculoskeletal disorders
- Pregnant individuals
- Individuals with fractures or deformities of the spine or related areas
- Individuals with sensory deficits
- Individuals who engaged in activities that could affect the study results (e.g., medication use, alcohol consumption, or excessive exercise) within 24 hours prior to participation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: The combined diaphragmatic breathing and trunk stabilization exercise group
The combined diaphragmatic breathing and trunk stabilization exercise group performed trunk stabilization exercises consisting of dead bug, bridge, side plank, and bird dog, with additional diaphragmatic breathing exercise.
|
Trunk stabilization exercises consisting of dead bug, bridge, side plank, and bird dog were performed for 10 repetitions in 3 sets, while the side plank was performed for 5 repetitions with a 10-second hold for 3 sets.
Rest intervals between sets were set at 1 minute.
diaphragmatic breathing exercise was performed in a crook-lying position with one hand placed on the sternum and the other on the abdomen.
Participants were instructed to inhale through the nose for 5 seconds, allowing lateral expansion of the rib cage, and exhale through pursed lips for 10 seconds while minimizing chest movement.
The breathing exercise was performed for 10 repetitions in 3 sets with 1-minute rest between sets.
|
|
Active Comparator: The trunk stabilization exercise group
The trunk stabilization exercise group performed trunk stabilization exercises consisting of dead bug, bridge, side plank, and bird dog
|
Trunk stabilization exercises consisting of dead bug, bridge, side plank, and bird dog were performed for 10 repetitions in 3 sets, while the side plank was performed for 5 repetitions with a 10-second hold for 3 sets.
Rest intervals between sets were set at 1 minute.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pain intensity
Time Frame: Baseline and Week 4
|
Pain intensity was measured using the Visual Analogue Scale (VAS), a 0-10 cm scale where 0 indicates no pain and 10 indicates the worst imaginable pain.
|
Baseline and Week 4
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional disability
Time Frame: Baseline and Week 4
|
Functional disability was assessed using the Korean version of the Oswestry Disability Index (KODI).
The total score ranges from 0 to 100, with higher scores indicating greater disability.
Disability levels are interpreted as follows: 0-20 (minimal disability), 21-40 (moderate disability), 41-60 (severe disability), 61-80 (crippled), and 81-100 (bed-bound or exaggerating symptoms).
|
Baseline and Week 4
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle activity
Time Frame: Baseline and Week 4
|
Muscle activity was measured using surface electromyography (sEMG) of the rectus abdominis, external oblique, internal oblique, and erector spinae, expressed as %MVIC.
|
Baseline and Week 4
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 23, 2025
Primary Completion (Actual)
February 23, 2025
Study Completion (Actual)
April 8, 2025
Study Registration Dates
First Submitted
April 29, 2026
First Submitted That Met QC Criteria
April 29, 2026
First Posted (Actual)
May 6, 2026
Study Record Updates
Last Update Posted (Actual)
May 11, 2026
Last Update Submitted That Met QC Criteria
May 6, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SYU 2024-11-004-007
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data (IPD) will not be shared due to ethical and privacy considerations.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Low Back Pain
-
University of Kansas Medical CenterCompletedLower Back Pain | Low Back Pain | Low Back Pain, Mechanical | Low Back Pain, Recurrent | Low Back Pain, Postural | Postural Low Back Pain | Mechanical Low Back Pain | Low Back Ache | Recurrent Low Back Pain | Lower Back Pain Chronic | Low Back Pain, Posterior Compartment | Low BackacheUnited States
-
Istanbul UniversityIstinye UniversityCompletedLow Back Pain | Low Back Pain, Mechanical | Low Back Pain, Recurrent | Low Back Pain, PosturalTurkey
-
Dow University of Health SciencesRecruitingLow Back Pain | Chronic Low-back Pain | Low Back Pain, Mechanical | Mechanical Low Back Pain | Pain, Chronic | Pain, Back | Lower Back Pain Chronic | CLBP - Chronic Low Back PainPakistan
-
Faculdade de Ciências Médicas da Santa Casa de...CompletedLow Back Pain, Mechanical | Low Back Pain, Postural | Lower Back Pain Chronic | Low Back Pain, Posterior CompartmentBrazil
-
General Incorporated Foundation Ryukyuseimeisaiseikai...CompletedChronic Low Back Pain | Non-specific Low Back Pain | Low Back Pain (LBP)Japan
-
University School of Physical Education in WroclawCompletedLow Back Pain | Low Back Pain, Mechanical | Low Back Pain, PosturalPoland
-
Texas Woman's UniversityTexas Physical Therapy AssociationCompletedLow Back Pain | Chronic Low Back Pain | Subacute Low Back PainUnited States
-
University of ParmaKing's College London; Helmholtz Zentrum München; GENOS; Ip Research Consulting... and other collaboratorsUnknownChronic Low Back Pain | Acute Low Back PainUnited States, Australia, Belgium, Croatia, Italy, United Kingdom
-
Karolinska InstitutetCompletedChronic Low Back Pain | Recurrent Low Back Pain | Persistent Low Back PainSweden
-
Ache Laboratorios Farmaceuticos S.A.Unknown
Clinical Trials on trunk stabilization exercise
-
University of VermontEunice Kennedy Shriver National Institute of Child Health and Human Development...Completed
-
University of Social Welfare and Rehabilitation...CompletedLow Back PainIran, Islamic Republic of
-
Khon Kaen UniversityCompleted
-
Inje UniversityUnknown
-
Bundang CHA HospitalNot yet recruiting
-
Istanbul University - Cerrahpasa (IUC)Completed
-
University of VermontEunice Kennedy Shriver National Institute of Child Health and Human Development...Completed
-
Riphah International UniversityCompleted
-
Riphah International UniversityRecruitingBasketball PlayersPakistan
-
Drexel UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development...Completed