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Diaphragmatic Release for Low Back Pain

Investigating the Effectiveness of Diaphragmatic Release in Patients With Low Back Pain.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07298109
Enrollment
42
Registered
2025-12-23
Start date
2025-12-11
Completion date
2026-12-15
Last updated
2025-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diaphragm; Relaxation, Low Back Pain

Brief summary

Low back pain is one of the most common musculoskeletal disorders, significantly affecting the quality of life of individuals. In non-specific low back pain, a lack of stabilization in the core region negatively impacts the performance of activities. The diaphragm forms the framework of the core region, and its dysfunction can contribute to both respiratory problems and low back pain. This study will investigate the effects of diaphragm relaxation, added to spinal stabilization exercises, on pain, disability, quality of life, central sensitization, and trunk muscle endurance.

Detailed description

Low back pain is one of the most common musculoskeletal problems, limiting daily life activities, leading to loss of productivity, and significantly reducing quality of life. In non-specific low back pain, insufficient stabilization in the trunk region and inadequate activation of deep muscles reduce the effectiveness of functional movements and contribute to chronic pain. The diaphragm, a crucial component of trunk stability, plays a critical role not only in respiratory function but also in maintaining spinal stability through the regulation of intra-abdominal pressure. Dysfunction or insufficient relaxation of the diaphragm can lead to changes in breathing patterns, impaired postural control, and persistent low back pain. Therefore, a better understanding of the diaphragm's role in low back pain mechanisms and its targeting in therapeutic interventions is becoming increasingly important. This study aims to investigate the effects of diaphragm relaxation techniques, applied in addition to spinal stabilization exercises, on pain intensity, disability level, quality of life, central sensitivity, and trunk muscle endurance.

Interventions

In addition to spinal stabilization exercises, patients will perform diaphragmatic relaxation exercises three days a week for eight weeks.

OTHERControl

Patients will undergo spinal stabilization exercises three times a week for eight weeks.

Sponsors

Karabuk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Masking description

Double blind (Participant, Investigator)

Intervention model description

Parallel Assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Being between 18-65 years of age * Having been diagnosed with chronic non-specific lower back pain (pain between the gluteal folds and the 12th ribs lasting at least 12 weeks and without a known pathoanatomical cause) * Being willing to participate in the study

Exclusion criteria

* Psychological disorders, mental disorders, cancer, and severe depression * History of primary or metastatic spinal malignancy or spinal fracture * Neurological disease (Hemiplegia, Multiple Sclerosis, Parkinson's, etc.) * Having been diagnosed with advanced osteoporosis * Having undergone previous surgery or had an acute infection in the lumbar region

Design outcomes

Primary

MeasureTime frameDescription
Pain severityBaseline, After intervention (eight week later)The severity of back pain will be assessed using the Visual Analog Scale (VAS). Patients choose the appropriate score between 0 and 10. Higher scores indicate higher pain levels.
Central sensitizationBaseline, After intervention (eight week later)Central sensitization will be assessed with the Central Sensitization Scale. The total score range is between 0-100 points. As the score increases, sensitization increases and 40 points and above are considered higher sensitization.
Disability levelsBaseline, After intervention (eight week later)Disability will be measured by the Oswestry Disability Index. The total score ranges from 0-100 and the higher the score, the higher the level of disability.
Quality of life levelBaseline, After intervention (eight week later)In the SF-36 quality of life assessment, each sub-parameter is scored on a scale of 0. 0 is the lowest score and 100 is the highest.
Trunk muscle enduranceBaseline, After intervention (eight week later)The endurance of the trunk flexor and extensor muscles will be evaluated. Increasing the duration of the test indicates an increase in endurance.

Countries

Turkey (Türkiye)

Contacts

Primary ContactMusa Güneş, PhD
musagunes@karabuk.edu.tr03704789081

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026