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

Primary Purpose

Low Back Pain, Trigger Point Pain, Myofascial

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Jones Group (Strain Counterstrain)
Myofascial Induction Group
Placebo Group
Sponsored by
Universidad Católica San Antonio de Murcia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain focused on measuring Physiotherapy, Rehabilitation, Treatment, Active Trigger Point

Eligibility Criteria

19 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Universidad Católica de Murcia

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Jones Group (Strain Counterstrain)

Myofascial Induction Group

Placebo Group

Arm Description

Jones Group consist in 90 seconds in a ralease positioning of no pain in muscle acortation

Myofascial Induction Group consist in 15 minutes of superficial and deep lumbar fascia maneuvers

Placebo Group only have to mantain no pain positioning for 3 minutes

Outcomes

Primary Outcome Measures

Pain intensity
Measured with Numeric Rating Scale wich consist in measure pain intensity with a score of 0-10
Pression algometer
Measures pressure pain thresholds

Secondary Outcome Measures

Spinal test
Measured 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 test
Measured with Baiobit software counter movement jump test wich consist a velocity, height and accuracy evaluation of a vertical jump

Full Information

First Posted
February 7, 2022
Last Updated
May 19, 2022
Sponsor
Universidad Católica San Antonio de Murcia
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1. Study Identification

Unique Protocol Identification Number
NCT05279794
Brief Title
Efficacy of Two Types of Non-invasive Erector Spinae Muscle Taut Band Therapy in University Students With Low Back Pain
Official Title
Efficacy of Two Types of Non-invasive Erector Spinae Muscle Taut Band Therapy in University Students With Low Back Pain: A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
March 21, 2022 (Actual)
Primary Completion Date
March 23, 2022 (Actual)
Study Completion Date
May 19, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad Católica San Antonio de Murcia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain, Trigger Point Pain, Myofascial
Keywords
Physiotherapy, Rehabilitation, Treatment, Active Trigger Point

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Jones Group (Strain Counterstrain)
Arm Type
Experimental
Arm Description
Jones Group consist in 90 seconds in a ralease positioning of no pain in muscle acortation
Arm Title
Myofascial Induction Group
Arm Type
Active Comparator
Arm Description
Myofascial Induction Group consist in 15 minutes of superficial and deep lumbar fascia maneuvers
Arm Title
Placebo Group
Arm Type
Placebo Comparator
Arm Description
Placebo Group only have to mantain no pain positioning for 3 minutes
Intervention Type
Other
Intervention Name(s)
Jones Group (Strain Counterstrain)
Intervention Description
No pain positioning technique with diaphragmatic breathing
Intervention Type
Other
Intervention Name(s)
Myofascial Induction Group
Intervention Description
Myofascial Induction technique on the lumbar fascia
Intervention Type
Other
Intervention Name(s)
Placebo Group
Intervention Description
No pain positioning of participants
Primary Outcome Measure Information:
Title
Pain intensity
Description
Measured with Numeric Rating Scale wich consist in measure pain intensity with a score of 0-10
Time Frame
20 minutes
Title
Pression algometer
Description
Measures pressure pain thresholds
Time Frame
20 minutes
Secondary Outcome Measure Information:
Title
Spinal test
Description
Measured with Baiobit Software. The range of movement will be measured in grades as per: flexion/extension; right/left rotation; and right/left inclination
Time Frame
20 minutes
Title
Countermovement jump test
Description
Measured with Baiobit software counter movement jump test wich consist a velocity, height and accuracy evaluation of a vertical jump
Time Frame
20 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Facility Information:
Facility Name
Universidad Católica de Murcia
City
Murcia
ZIP/Postal Code
30107
Country
Spain

12. IPD Sharing Statement

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

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