Abdominal Wall Evaluation in Low Back Pain

December 6, 2011 updated by: University of Sao Paulo General Hospital

Deep Abdominal Wall Muscle Dysfunction During Calm Respiration in Chronic Low Back Pain Patients

The purpose of this study was to evaluate feed-forward contraction of the transversus abdominis and thickness of the transversus abdominis, obliquus internus, and obliquus externus during calm and standardized respiration in low back pain patients and pain-free subjects.

Study Overview

Status

Completed

Detailed Description

Low back pain patients have alterations in abdominal wall function, especially in the feed-forward activation of transversus muscle during limbs movements. However, there are no reports on the abdominal function in low back pain patients during physiological respiratory movement.

Study Type

Observational

Enrollment (Actual)

39

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

      • São Paulo, Brazil, 05403-000
        • Physical Therapy, Speech and Occupational Therapy Department, School of Medicine: University of São Paulo, Brazil

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

20 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Community sample

Description

Inclusion Criteria:

  • For the low back pain group: women with history of non-specific chronic low back pain for more than three months
  • For the pain-free group: pain-free women

Exclusion Criteria:

  • For both groups were: pregnancy, neurological condition, obesity (body mass index: BMI >30), or previous spine or abdominal surgery.
  • For the low back pain group: rheumatology diseases other than low back pain.
  • For the pain-free group: any rheumatology disease.

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

Cohorts and Interventions

Group / Cohort
Nineteen women with low back pain
Twenty pain-free women

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Clarice Tanaka, PhD, Full Professor - Department of Physical Therapy, Communication Science & Disorders, Occupational Therapy, Faculty of Medicine - USP
  • Study Chair: Patricia R Patarro, Physical Therapy, Speech and Occupational Therapy Department, School of Medicine: University of São Paulo, Brazil
  • Study Chair: Renato A Sernik, Institute of Radiology, School of Medicine: University of São Paulo, Brazil
  • Study Chair: Débora M Meira, Physical Therapy, Speech and Occupational Therapy Department, School of Medicine: University of São Paulo, Brazil
  • Study Chair: América C Fracini, Physical Therapy, Speech and Occupational Therapy Department, School of Medicine: University of São Paulo, Brazil
  • Study Chair: Cássio M Siqueira, Physical Therapy, Speech and Occupational Therapy Department, School of Medicine: University of São Paulo, Brazil

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

December 1, 2009

Primary Completion (Actual)

November 1, 2010

Study Completion (Actual)

November 1, 2010

Study Registration Dates

First Submitted

December 6, 2011

First Submitted That Met QC Criteria

December 6, 2011

First Posted (Estimate)

December 8, 2011

Study Record Updates

Last Update Posted (Estimate)

December 8, 2011

Last Update Submitted That Met QC Criteria

December 6, 2011

Last Verified

December 1, 2011

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • FRACINI

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.

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