MedPath

Short-term Effects of Exercise Program Versus Electropuncture in Patients With Chronic Non-specific Low Back Pain: A Randomized Clinical Trial.

Not Applicable
Completed
Conditions
Exercise Program
Electroacupuncture
Low Back Pain
Interventions
Other: Percutaneous electrostimulation treatment (EPS)
Other: Exercise program
Registration Number
NCT03794869
Lead Sponsor
Universidad de Almeria
Brief Summary

This study evaluate the effectiveness that exists when performing a treatment based on a table of exercises for strengthening the lumbar muscles versus a treatment based on electropuncture in patients with chronic low back pain.

Detailed Description

Low back pain has a high prevalence in all European countries, appearing as the main cause of activity limitation in people under 45 years of age. It has got a high recurrence, which decreases the activities of daily life, facilitates the focus of attention to pain and increases the fear of movement, with the consequent muscular atrophy. A serie cases will be conducted comparing a a table of exercises versus electropuncture.

Objective: Evaluate the effectiveness that exists when performing a tratment based on a table of exercises for strengthening the lumbar muscles versus a treatment based on electropuncture.

Methods: A sample of 12 subjects with chronic low back pain will be assigned to an exercise program or dry electropuncture treatment (EPS), during 4 weeks (2 sessions/week). The measurement variables selected for the study were the followings: Straight Leg Raise, Vasalva, Gaesslen test, algometry (pressure pain threshold), goniometry (measurement of the range of motion), Scale of disability for low back pain of Oswestry, Beck's Depression Inventory (BDI), Visual Analogue Scale (EVA), Mcquade's Test and the Roland-Morrys' Questionnaire, developing a pre-treatment and post-treatment assessment.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
68
Inclusion Criteria
  • Chronic non-specific low back pain persisting ≥ 3 months.
  • Age between 25 and 60 years.
  • Not currently receiving physical therapy.
Read More
Exclusion Criteria
  • Presence of lumbar stenosis.
  • Presence of clinical signs of radiculopathy.
  • Diagnosis of spondylolisthesis.
  • Diagnosis of fibromyalgia.
  • Treatment with corticosteroid or pharmachological medication within the paset 2 weeks.
  • A history of spinal surgery.
  • Central or peripheral nervous system disease
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Exercise programPercutaneous electrostimulation treatment (EPS)It will be consist in a program of lumbo-pelvic stabilization exercises and strengthening of the core: awareness of breathing, front and side plate abdominal, glute bridge/hip elevations, lift extended leg, pelvic tilt, hamstring stretch, strengthening lower abdominals, cat-camel posture, trunk rotations with flexed knees, rolling in sitting and lumbar extension with hip extensión in prone
Percutaneous electrostimulation treatment (EPS)Exercise programApply dry needles in a tight band of some of the muscles that most affect the appearance of low back pain, such as: paravertebral, lumbar quadrate, gluteus medius and pyramidal, and administer analgesic microcurrents.
Primary Outcome Measures
NameTimeMethod
AlgometryAt baseline and immediate post-treatment

An instrument for measuring the degree of sensitivity to pain.

Secondary Outcome Measures
NameTimeMethod
Beck's Depression InventoryAt baseline and immediate post-treatment

The state of depression will be determined with the Beck Depression Inventory (BDI), a self-applied 21-item questionnaire that assesses a wide spectrum of depressive symptoms. It focuses on the cognitive components of depression, which represent around 50% of the total questionnaire score.

GoniometryAt baseline and immediate post-treatment

Measurement of the range of motion

Mcquade TestAt baseline and immediate post-treatment

It measures the isometric endurance of trunk flexion muscles

Visual Analog ScaleAt baseline and immediate post-treatment

Pain will be assessed with the Visual Analog Scale (VAS), which assesses the pain intensity and degree of relief experienced by the patient (scored of 0 = no pain; 10 = unbearable pain).

Oswestry Low Back Pain Disability Index.At baseline and immediate post-treatment

It has 10 items associated to activities of daily living, each item has a puntuation fron 0 to 5 points

Roland-Morrys' QuestionnaireAt baseline and immediate post-treatment

This is a self-reported questionnaire consisting in 24 items reflecting limitations in different activities of daily living attributed to low back pain including walking, vending over, sitting, lying down, dressing, sleeping, self-care and daily activities

Trial Locations

Locations (1)

Almeria University

🇪🇸

Almeria, Spain

© Copyright 2025. All Rights Reserved by MedPath