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Comparison of the Effects of Physical Therapy With and Without Magnetic Field Therapy in People With Low Back Pain

Comparison of the Effects of Physical Therapy With and Without Magnetic Field Therapy in People With Low Back Pain

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05202691
Enrollment
40
Registered
2022-01-21
Start date
2022-03-31
Completion date
2023-03-31
Last updated
2022-01-21

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

Conditions

Low Back Pain

Keywords

low back pain, physical therapy, rehabilitation, magnetic field therapy

Brief summary

A randomized and controlled trial to people with low back pain who are divided into 2 groups of treatment: 1- people treated with a protocol of physical therapy techniques without magnetic field therapy; 2- people treated with the same protocol of physical therapy techniques adding a magnetic stimulation treatment. The interventions are conducted in 3 sessions provided during 3 weeks.The lumbar pain and disability are assessed before and after the intervention, and lumbar flexion and extension pain are assessed before and after each session in all the participants.

Detailed description

This study is a randomized controlled trial evaluating clinical effects of a protocol of Physical Therapy Treatment (PTT), via manual therapy and active mobilization, adding or not a magnetic field therapy in people with non-specific low back pain lasting at least 6 weeks. Participants were randomized to receive either a PTT protocol including a magnetic stimulation treatment or the same PTT protocol with a sham magnetic intervention. The interventions are conducted in 3 sessions provided during 3 weeks. Intervention: A description of the 2 groups of treatment: 1. \- Experimental group 1: a protocol of physical therapy treatment including: * Manual therapy techniques for inhibition of piriformis, quadratus lumbar, and paravertebral muscles in prone position and bilaterally. * 2 functional techniques applied to the sacrum in prone position. * A myofascial release of ligaments inserted to the sacrum in prone position and bilaterally. * Manual therapy technique for inhibition of psoas-iliacus muscle in supine position and bilaterally. * Stretching techniques of piriformis, gluteal and paravertebral muscles in supine position and bilaterally. * Active gluteus maximus contraction in supine position bilaterally. To this protocol, a 15 minutes of magnetic field therapy treatment applied to the lumbosacral region in prone position is added. 2. \- Experimental group 2: the same Physical Therapy Treatment protocol with a sham magnetic intervention applying in the same region with a disconnected device during 15 minutes.

Interventions

OTHERGroup 1 (Physical Therapy+Magnetic Field Therapy)

A Physical Therapy Protocol (including manual therapy, stretching and exercise for low back pain) adding a Magnetic Field Therapy using the Zimmer EmfieldPro device (Zimmer MedizinSysteme, Germany)

OTHERGroup 2 (Physical Therapy)

A Physical Therapy Protocol (including manual therapy, stretching and exercise for low back pain)

Sponsors

Universidad Complutense de Madrid
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

To participants: the intervention applied to both groups is the same Physical Therapy Treatment protocol and the use of the same magnetic field therapy device during the same time (for the sham group: the device is disconnected and the sound is simulated with a recording). The investigator assessing the outcomes is blinded to the group assignments

Intervention model description

This study is a randomized controlled trial evaluating clinical effects in people with low back pain who are divided into 2 groups of treatment, where the interventions are conducted in 3 sessions provided during 3 weeks.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* The inclusion criteria were individuals aged between 18 and 65 years with a diagnosis of non-specific low back pain, with or without lower limb irradiation, lasting at least 6 weeks.

Exclusion criteria

* Pregnancy, spinal tumor or infection, diabetes, spinal fracture or previous spine surgery. * Patients with a history of rehabilitation treatment for back pain within the preceding month * Unstable medical disorder not controlled by standard treatment and those with a cardiac pacemaker or using any other electrical devices or prosthesis.

Design outcomes

Primary

MeasureTime frameDescription
Lumbar pain change with the Pain Detect QuestionnaireChange from Baseline Lumbar pain at 4 weeks.lumbar pain at this moment and in the last 4 weeks evaluated with the Pain Detect Questionnaire. The Questionnaire has a maximum score of 35 and a minimum score of 0. Lower scores mean a better outcome.
Disability Questionnaire 1 changeChange from Baseline degree of diability at 4 weeks.Disability Questionnaire assessed with the Roland-Morris Questionnaire. The Questionnaire has a maximum score of 24 and a minimum score of 0. Lower scores mean a better outcome.
Disability Questionnaire 2 changeChange from Baseline degree of diability at 4 weeks.Disability Questionnaire 2 assessed with the Oswestry Disability Index. The Oswestry Disability Index is scored from 0 (absence of disability) to 100 (maximum disability). This questionnaire has 10 multiple-choice questions, each of which may be scored between 0 (no disability) and 5 (maximum disability). Lower scores mean a better outcome.

Secondary

MeasureTime frameDescription
Lumbar flexion Numerical Rating Scale4 weeks (immediately before and after each of the sessions)Lumbar flexion evaluated with a Numerical Rating Scale. The minimum value is 0 and the maximum value is 10. Lower scores mean a better outcome.
Lumbar extension Numerical Rating Scale4 weeks (immediately before and after each of the sessions)Lumbar extension evaluated with a Numerical Rating Scale. The minimum value is 0 and the maximum value is 10. Lower scores mean a better outcome.
Finger to Floor test4 weeks (immediately before and after each of the sessions)Lumbar mobility evaluated with the finger-to-floor test, assessed before and after each session in all the participants. The minimum value is 0 centimeters and the maximum value depending the flexibility os each participant and the distance, in centimeters between fingers anthe floor. Lower distance in centimeters means a better outcome.

Countries

Spain

Contacts

Primary ContactIsidro Fernández-López, Dr.
isidrofelo@gmail.com+34625598970
Backup ContactPablo Llanes-Ontiveros, Mr.
pablo_llanes@hotmail.com+34629234854

Outcome results

None listed

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