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Effects of Diaphragmatic Manual Therapy in Chronic Low Back Pain

Effects of Diaphragmatic Manual Therapy in Chronic Low Back Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02343185
Enrollment
64
Registered
2015-01-21
Start date
2014-01-31
Completion date
2016-06-30
Last updated
2017-08-08

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

Conditions

Low Back Pain

Keywords

diaphragm, osteopathic treatment, myofascial release

Brief summary

This study is a double-blind randomized clinical trial with two arms which aims to study the effects of diaphragmatic treatment in patients with nonspecific low back pain. Low back pain has a great importance in today's society, and it is therefore important to develop an effective treatment for this condition. People with chronic nonspecific low back pain, can present respiratory disorders and get anxiety states, affecting mainly the diaphragm muscle. Therefore, given its direct anatomic relationship, the diaphragm may be part of the development of chronic low back pain. Although clinical practice guidelines for chronic low back pain have been developed, it hasn't been explored before a physiotherapy treatment especially aimed at a diaphragmatic treatment. A double-blind randomized clinical trial with two arms will be used for this purpose, 64 patients with nonspecific low back pain referred from different hospitals of Castellón will be randomized into two groups: * Diaphragmatic intervention with osteopathic manual therapy treatment (D). * Diaphragmatic intervention with placebo treatment group (P). An osteopathic manual therapy protocol for the treatment of back pain including techniques for the diaphragm muscle will be applied to the patients in group D, in a total of 5 sessions. For patients in group P, the same protocol will be performed on the diaphragm but with placebo treatment techniques. The study focuses on the analysis of the following variables: scores on the questionnaires: * Pain: McGill Pain Questionnaire and VAS (Visual Analogical Scale ). * Fear Avoidance: (FABQ) * Disability: Oswestry Disability Index and Roland-Morris * Anxiety: HADS: (Hospital Anxiety and Depression Scale) * Catastropizing: PCS (Pain Catastropizing Scale) * Satisfaction with treatment (Escala de Satisfacción con el tratamiento) The results of these pre-intervention and post-intervention variables will be compared between the two groups in the first session, in the fourth session and in the first and third month after the first intervention. The VAS score will also be assessed in the second and third session.

Interventions

OTHERmanual therapy with diaphragmatic treatment

Subjects receive five sesions of manual therapy for low back pain combined with diaphragmatic treatment.

OTHERPlacebo treatment

Subjects receive five sesions of manual therapy for low back pain combined with a sham diaphragmatic treatment.

Sponsors

Cardenal Herrera University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* low back pain for more than 3 months

Exclusion criteria

* vertebra fracture * systemic disease * spinal surgery * degenerative articular disease * acute soft tissue inflammation * radiculopathy * structural spine deformities * pregnancy * mental disease * dermatologic disease * rejection to manual contact

Design outcomes

Primary

MeasureTime frameDescription
Pain4 weeksShort form McGill Pain Questionnaire
Disability4 weeksOswestry Disability Index

Secondary

MeasureTime frameDescription
Fear Avoidance Beliefs Questionnaire4 weeksFABQ
Hospital Anxiety and Depression Scale4 weeks
Pain Catastropizing Scale4 weeks
Satisfaction with treatment Questionnaire4 weeks

Countries

Spain

Outcome results

None listed

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