Lumbar and Gluteal Motor Control in Chronic Low Back Pain
ConditionLow Back Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity of Castilla-La Mancha
About this trial
The present study aims to evaluate the effectiveness of an 8-week combined lumbar motor control and gluteal muscle strengthening program in individuals with chronic non-specific low back pain
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age between 18 and 65 years.
Non-specific low back pain with an intensity greater than 3/10 on a visual analogue scale.
Symptom duration longer than 3 months.
Sufficient understanding of spoken and written Spanish to adequately comprehend the intervention instructions and complete the assessments.
Disqualifiers
Severe lumbar or hip trauma within the previous 6 weeks.
Prior vertebral fracture or lumbar disc herniation.
Fibromyalgia.
Active oncological disease.
Trial design
Design model
Parallel
Treatments tested in this trial
Lumbar motor control exercises
Device24 sessions over an 8-week period, at a frequency of three sessions per week (on alternating days -Monday, Wednesday, and Friday-); 60min/session.
Gluteal strengthening exercises
DeviceGluteal strengthening exercises will be performed in the same days as lumbar motor control program.
Treatment groups
54 Participants
are divided into 2 treatment groupsGroup A: Lumbar motor control + Gluteal exercisesExperimental treatment 2 interventions
Group B: Lumbar motor controlExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Pain intensity
It will be measured with a visual analog scale (VAS) of 100 millimeters in length. The subject has to indicate the level of pain he feels, being 0 the absence of pain and 100 the maximum imaginable.
Time frame
Baseline; inmediately after intervention.Secondary outcomes
1
Functionality
The version adapted to Spanish from the Oswestry Disability Index (ODI) will be used. It comprises 10 items, each scored from 0 to 5 (from no limitation to maximum limitation). The total score (0-100%) is calculated by dividing the sum of the item scores by the maximum possible score and multiplying by 100.
Time frame
Baseline; inmediately after intervention.Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: