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

Sponsor
Universidad Complutense de Madrid (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05202691
Collaborator
(none)
40
1
2
12
3.3

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Group 1 (Physical Therapy+Magnetic Field Therapy)
  • Other: Group 2 (Physical Therapy)
N/A

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:
    • 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.

    • 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
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.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.
Masking:
Triple (Participant, 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
Primary Purpose:
Treatment
Official Title:
Comparison of the Effects of Physical Therapy With and Without Magnetic Field Therapy in People With Low Back Pain
Anticipated Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
May 1, 2022
Anticipated Study Completion Date :
Mar 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group 1 (Physical Therapy+Magnetic Field Therapy)

Physical Therapy Protocol plus Magnetic Field Therapy A protocol of physical therapy treatment including: Manual therapy techniques for inhibition of piriformis, quadratus lumbaris, 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 using the Zimmer EmfieldPro device (Zimmer MedizinSysteme, Germany) applied to the lumbosacral region in prone position is added.

Other: Group 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)
Other Names:
  • physical therapy and magnetic field therapy for low back pain
  • Active Comparator: Group 2 (Physical Therapy)

    Physical Therapy Protocol alone: The same Physical Therapy Treatment protocol with a sham magnetic intervention applying in the same region with a disconnected Zimmer EmfieldPro device (Zimmer MedizinSysteme, Germany) during 15 minutes.

    Other: Group 2 (Physical Therapy)
    A Physical Therapy Protocol (including manual therapy, stretching and exercise for low back pain)
    Other Names:
  • physical therapy for low back pain
  • Outcome Measures

    Primary Outcome Measures

    1. Lumbar pain change with the Pain Detect Questionnaire [Change 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.

    2. Disability Questionnaire 1 change [Change 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.

    3. Disability Questionnaire 2 change [Change 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 Outcome Measures

    1. Lumbar flexion Numerical Rating Scale [4 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.

    2. Lumbar extension Numerical Rating Scale [4 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.

    3. Finger to Floor test [4 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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts 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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Complutense University of Madrid Madrid Spain

    Sponsors and Collaborators

    • Universidad Complutense de Madrid

    Investigators

    • Principal Investigator: Isidro Fernández-López, Dr., Complutense University of Madrid

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Universidad Complutense de Madrid
    ClinicalTrials.gov Identifier:
    NCT05202691
    Other Study ID Numbers:
    • ComplutenseHolystic
    First Posted:
    Jan 21, 2022
    Last Update Posted:
    Jan 21, 2022
    Last Verified:
    Dec 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Universidad Complutense de Madrid
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 21, 2022