Skip to content

Efficacy of Two Types of Non-invasive Erector Spinae Muscle Taut Band Therapy in University Students With Low Back Pain

Efficacy of Two Types of Non-invasive Erector Spinae Muscle Taut Band Therapy in University Students With Low Back Pain: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05279794
Enrollment
60
Registered
2022-03-15
Start date
2022-03-21
Completion date
2022-05-19
Last updated
2022-05-20

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

Conditions

Low Back Pain, Trigger Point Pain, Myofascial

Keywords

Physiotherapy, Rehabilitation, Treatment, Active Trigger Point

Brief summary

Non-specific low back pain can be caused by the presence of active trigger points in the muscles of the lumbopelvic region. Trigger points are defined as hypersensitive points within a taut band of a musculoskeletal system that cause pain during contraction, stretching, or stimulation of said muscle. If these points are active, they can trigger referred pain, local tenderness, and vegetative responses. There is scientific evidence of the improvement of the treatment of these points through non-invasive manual techniques. The objective of this study will be to determine the effect of Strain Counterstrain and Myofascial Induction techniques in subjects with low back pain secondary to the presence of active trigger points in the lumbopelvic region. Hyperexcitable myofascial trigger points located within a taut band of skeletal muscle or fascia cause referred pain, local tenderness, and autonomic changes. The scientific data refer to an immediate improvement in the symptoms of these active points treated with manual therapy. Based on these factors, the objective of the study is to determine the effect of the combined therapy of the Strain Counterstrain technique and Myofascial Induction in participants with the presence of an active trigger point in the erector spinae muscle.

Detailed description

The treatment will last a total of 15 minutes accompanied by a baseline assessment and after 10 minutes of the intervention in 2 experimental groups and a placebo group, of no-pain positioning. In addition to basic indices and scales of low back pain and disability caused by low back pain, it is intended to measure flexibility, range of motion, proprioception and cognition through software with sensors of the latest technology when representing reliable results in differences between techniques.

Interventions

No pain positioning technique with diaphragmatic breathing

OTHERMyofascial Induction Group

Myofascial Induction technique on the lumbar fascia

OTHERPlacebo Group

No pain positioning of participants

Sponsors

Universidad Católica San Antonio de Murcia
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
19 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Presence of low back pain * Presence of active trigger point in the erector spinae as described by Lawrence H. Jones

Exclusion criteria

* Participants who present dizziness, vertigo; * Previous or scheduled surgeries in the lumbar spine and/or lower extremities; * Suspicion of serious fractures or pathologies (tumor, inflammation, infection, rheumatological disorder, systemic disease, presence of fever); * Diagnosis of radiculopathy or neuropathy; * Structural deformity in the spine; spondyloarthropathy, disabling pain and physical disability; * Use of pain relievers or anti-inflammatory drugs in the last 48 hours; * Neurological or psychiatric disorder; * Presence or suspicion of pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity20 minutesMeasured with Numeric Rating Scale wich consist in measure pain intensity with a score of 0-10
Pression algometer20 minutesMeasures pressure pain thresholds

Secondary

MeasureTime frameDescription
Spinal test20 minutesMeasured with Baiobit Software. The range of movement will be measured in grades as per: flexion/extension; right/left rotation; and right/left inclination
Countermovement jump test20 minutesMeasured with Baiobit software counter movement jump test wich consist a velocity, height and accuracy evaluation of a vertical jump

Countries

Spain

Outcome results

None listed

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