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Transversus Abdominis Muscular Training and Chronic Low Back Pain

Effectiveness of Transversus Abdominis Muscular Training in Patients With Chronic Low Back Pain

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02374970
Enrollment
50
Registered
2015-03-02
Start date
2015-02-28
Completion date
2016-02-29
Last updated
2015-03-02

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

Conditions

Low Back Pain

Brief summary

Low back pain is not a diagnosis; it is a symptom describing the presence of pain in the lumbar vertebral or paravertebral region without any reference to the structure or cause of the process. It is one of the most widespread diseases and one of the most common reasons for visits in primary care setting. Exercises to improve lumbar stability involving co-contraction of the transversus abdominis have proved to be effective in reducing pain and improving function. It has been stated by ultrasound images that specific stabilization exercises cause contraction of the deep abdominal muscles, but it remains unclear whether training produce thickness muscle improvement and if this improvement is related to clinical findings. To try to resolve this issue a project of an experimental trial, double-blind (patient and evaluator) with two groups randomly assigned is presented. All participants will be recruited in an primary care center of the Catalan Health Institut and will sign informed consent. All will receive a protocolized treatment with therapeutic exercises and thermotherapy and, additionally, those assigned to the intervention group were instructed in performing lumbar stability exercises. Pain (VAS), function (Roland-Morris Questionnaire) and the thickness of the transversus abdominis, internal and external oblique muscles (measured by ultrasound) at baseline, end of treatment protocol (12 sessions) and three months after the end of treatment will be assessed. Results in pain, function, and its correlation with the mean changes in the thickness of transversus abdominis will be analyzed.

Interventions

OTHERLumbar stability exercises

Four individualized learning sessions will be held during the same period of protocolized physiotherapy. Biofeedback training using the ultrasound machine will be performed in the first session, in order to show the specific contraction of the abdominal muscles with the stability exercises. The other three learning sessions will be performed without feedback, for the patient learn the exercises to make at home during the follow-up period.

Therapeutic exercises and thermotherapy during 12 daily sessions

Sponsors

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* 18 years old and over * Diagnosis of chronic low back pain (over 3 months) * Sign the informed consent form.

Exclusion criteria

* Non-stand supine position * Neural Irradiation pain * Previous surgical intervention in low back region * Heart pathology * Pregnancy * Pending litigation or legal claim * Poor language and communication skills making difficult to understand the informed consent

Design outcomes

Primary

MeasureTime frame
Change in transversus abdominis muscle thickness (Ultrasonography)Baseline, 15 days after, and three months after

Secondary

MeasureTime frame
Change in pain intensity (Visual analogue scale)Baseline, 15 days after, and three months after
Disability (Roland-Morris questionnaire)Baseline, 15 days after, and three months after
Change in internal oblique muscle thickness (Ultrasonography)Baseline, 15 days after, and three months after
Change in external oblique muscle thickness (Ultrasonography)Baseline, 15 days after, and three months after
Patient perception of change (Global Rating of Change scale)15 days after recruitment, and three months after

Countries

Spain

Contacts

Primary ContactEdurne Villar-Mateo
edurne.villar.mateo@gmail.com

Outcome results

None listed

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