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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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9 March 2015 |
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Main ID: |
NCT02374970 |
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Date of registration:
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19/02/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Transversus Abdominis Muscular Training and Chronic Low Back Pain
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Scientific title:
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Effectiveness of Transversus Abdominis Muscular Training in Patients With Chronic Low Back Pain |
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Date of first enrolment:
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February 2015 |
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Target sample size:
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50 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT02374970 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Spain
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Contacts
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Name:
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Edurne Villar-Mateo |
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Address:
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Telephone:
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Email:
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edurne.villar.mateo@gmail.com |
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Affiliation:
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Name:
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Edurne Villar-Mateo |
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Address:
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Telephone:
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Email:
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edurne.villar.mateo@gmail.com |
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Affiliation:
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Name:
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Edurne Villar-Mateo |
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Address:
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Telephone:
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Email:
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Affiliation:
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Jordi Gol Institut of Research in Primary Health Care |
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Key inclusion & exclusion criteria
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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
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Low Back Pain
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Intervention(s)
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Other: Protocolized Physiotherapy
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Other: Lumbar stability exercises
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Primary Outcome(s)
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Change in transversus abdominis muscle thickness (Ultrasonography)
[Time Frame: Baseline, 15 days after, and three months after]
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Secondary Outcome(s)
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Change in external oblique muscle thickness (Ultrasonography)
[Time Frame: Baseline, 15 days after, and three months after]
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Change in internal oblique muscle thickness (Ultrasonography)
[Time Frame: Baseline, 15 days after, and three months after]
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Change in pain intensity (Visual analogue scale)
[Time Frame: Baseline, 15 days after, and three months after]
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Disability (Roland-Morris questionnaire)
[Time Frame: Baseline, 15 days after, and three months after]
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Patient perception of change (Global Rating of Change scale)
[Time Frame: 15 days after recruitment, and three months after]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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