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Valuation of the Low Back Pain Treated With Different Types of Active Exercises in Women (ECOLUM)

Primary Purpose

Low Back Pain

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Core Stability Exercises (CSE)
Traditional Back School
TENS
Infra-red
Sponsored by
University Rovira i Virgili
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain focused on measuring Low Back Pain, Core stability exercise, Back school, TENS, Infra- red light

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Women aged 18 to 70 years.
  • Diagnosis of back pain from a trauma.
  • Untreated pain (except acetaminophen).
  • Informed consent.

Exclusion Criteria:

  • Algic process in the lumbar spine of infectious, neoplastic, metastasis, osteoporosis, inflammatory arthritis or fractures.
  • Cognitive impairment of any etiology.
  • Exercise intolerance for any reason.
  • Patients who have completed physical therapy in the last 3 months.
  • Patients who have received infiltration injections in the last 6 weeks.

Sites / Locations

  • Faculty of Medicine and Health SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Core Stability Exercises

Traditional Back School

Arm Description

Core Stability Exercises: 20 sessions, distributed daily, from Monday to Friday. The first 5 sessions are common in all patients in the study, and involves the application of infrared light (IR) (10 minutes) and TENS (20 minutes) to treat acute pain. From session number 6 to session 20, the patients will receive IR + TENS 2 days a week, and the other 3 days IR+TENS+Core Stability Exercises (25-30 minutes).

Traditional Back School: 20 sessions, distributed daily, from Monday to Friday. The first 5 sessions are common in all patients in the study, and involves the application of infrared light (IR) (10 minutes) and TENS (20 minutes) to treat acute pain. From session number 6 to session 20, the patients will receive IR + TENS 2 days a week, and the other 3 days IR+TENS+Traditional Back School (25-30 minutes).

Outcomes

Primary Outcome Measures

Changes in Visual Scale Analogue (VAS)
The VAS scale represents the pain intensity on a line of 10 cm, and one end there are the words "no pain" and the other end "the worst imaginable pain" written the distance in centimetres from the "no pain" point to the place marked by the patient represents the intensity of pain.

Secondary Outcome Measures

Changes in the Roland- Morris Disability Questionnaire
It consists of 24 items, which reflect limitation in different activities of daily living attributed by the patient to LBP. The patient must mark each item that applies to her current status. Scoring is also simple and fast; each checked item receives a score of 1, so scores range between 0 (no disability caused by LBP) and 24 (the maximum possible disability).

Full Information

First Posted
March 19, 2014
Last Updated
December 4, 2014
Sponsor
University Rovira i Virgili
Collaborators
Hospital Universitari Sant Joan de Reus
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1. Study Identification

Unique Protocol Identification Number
NCT02103036
Brief Title
Valuation of the Low Back Pain Treated With Different Types of Active Exercises in Women
Acronym
ECOLUM
Official Title
Valuation of the Low Back Pain Treated With Different Types of Active Exercises in Women
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Unknown status
Study Start Date
March 2014 (undefined)
Primary Completion Date
March 2015 (Anticipated)
Study Completion Date
October 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Rovira i Virgili
Collaborators
Hospital Universitari Sant Joan de Reus

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is determine whether the Core Stability Exercise is more effective than the traditional Back School for low back pain (LBP) in women.
Detailed Description
The aim of this study is to check what kind of exercises are the best to treat LBP with regard to clinical improvements. The secondary objectives are: to determine which treatment is more effective in improving pain in the fewest sessions possible, to determine the involvement of inflammatory biomarkers in the development of pain and revalue the results after one month of having finishing treatment. The project is a longitudinal, single-blind and randomized study with two treatment groups: GROUP 1: Infrared light+ Transcutaneous Electrical Nerve Stimulation (TENS) + Core Stability Exercises. GROUP 2: Infrared light + Transcutaneous Electrical Nerve Stimulation (TENS) + Traditional Back School. Duration of treatment: 4 weeks. The participants will performe the exercises in 20 daily sessions (Monday to Friday) guided by a physiotherapist. Following treatment with the physiotherapist, the participants should perform the exercises at home for 4 weeks at a rate of three times per week.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain
Keywords
Low Back Pain, Core stability exercise, Back school, TENS, Infra- red light

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Core Stability Exercises
Arm Type
Experimental
Arm Description
Core Stability Exercises: 20 sessions, distributed daily, from Monday to Friday. The first 5 sessions are common in all patients in the study, and involves the application of infrared light (IR) (10 minutes) and TENS (20 minutes) to treat acute pain. From session number 6 to session 20, the patients will receive IR + TENS 2 days a week, and the other 3 days IR+TENS+Core Stability Exercises (25-30 minutes).
Arm Title
Traditional Back School
Arm Type
Experimental
Arm Description
Traditional Back School: 20 sessions, distributed daily, from Monday to Friday. The first 5 sessions are common in all patients in the study, and involves the application of infrared light (IR) (10 minutes) and TENS (20 minutes) to treat acute pain. From session number 6 to session 20, the patients will receive IR + TENS 2 days a week, and the other 3 days IR+TENS+Traditional Back School (25-30 minutes).
Intervention Type
Procedure
Intervention Name(s)
Core Stability Exercises (CSE)
Other Intervention Name(s)
Motor control exercises, Specific spinal stabilitation exercises
Intervention Description
The increase in intra-abdominal pressure stiffens and strengthens the relevant structural support around the spine, compacts the arthrogenic structures and in combination with abdominal contraction, it can encourage a rigid cylinder and stiffness to occur around the spine. The relevant anatomy in these type of exercises are deep muscles like transversus abdominous, multifidus or pelvic floor. The participants will have to do 10 different exercises. They will have to perform from 8 to 10 repetitions of every exercise, guided by a physical therapist. They will be recommended about making some series more at home, three days a week, when the treatment was finished.
Intervention Type
Procedure
Intervention Name(s)
Traditional Back School
Intervention Description
The back school exercises are based in the traditional activity used for improve the back pain symptoms using the breathing with the stretching of the trunk muscles, the erector spinae reinforcement, the abdominal reinforcement or the postural movements. The participants will have to do 10 different exercises. They will have to perform from 8 to 10 repetitions of every exercise, guided by a physical therapist. They will be recommended about making some series more at home, three days a week, when the treatment was finished.
Intervention Type
Device
Intervention Name(s)
TENS
Other Intervention Name(s)
Transcutaneous Electrical Nerve Stimulation
Intervention Description
Used equipment: MEGASONIC 313 P4 (Carin). Application program number 15: analgesic TENS with stimulation of afferent fibers. Type of current: two-phase TNS. Width of the impulse: 70µs. Frequency of the impulse: 100Hz. Train: Not. Pause / pause activates: Not. Time of treatment: 20 minutes.
Intervention Type
Device
Intervention Name(s)
Infra-red
Other Intervention Name(s)
Infrared light
Intervention Description
Used equipment: INFRA - 2000 (Enraf Nonius) with the following parameters: 230 V / 50-60 Hz / 1.2 A
Primary Outcome Measure Information:
Title
Changes in Visual Scale Analogue (VAS)
Description
The VAS scale represents the pain intensity on a line of 10 cm, and one end there are the words "no pain" and the other end "the worst imaginable pain" written the distance in centimetres from the "no pain" point to the place marked by the patient represents the intensity of pain.
Time Frame
Pain was measured at the beginning of the study (session 0), and changes are evaluated again at sessions 10, 20, and 1 month later.
Secondary Outcome Measure Information:
Title
Changes in the Roland- Morris Disability Questionnaire
Description
It consists of 24 items, which reflect limitation in different activities of daily living attributed by the patient to LBP. The patient must mark each item that applies to her current status. Scoring is also simple and fast; each checked item receives a score of 1, so scores range between 0 (no disability caused by LBP) and 24 (the maximum possible disability).
Time Frame
Disability was measured at the beginning of the study (session 0), and changes are evaluated again at sessions 10, 20, and 1 month later.
Other Pre-specified Outcome Measures:
Title
Questionnaire of Physical Activity (ClassAF)
Description
Is a method developed by the Health Department of the Catalan Government. The ClassAF is a comprehensive questionnaire which contains a few items (1-4) to measure the general level of Physical Activity, it is calculated in METS (basal metabolic expenditure: mlO2/kg.min) and it allows to classify people into physically active or physically inactive.
Time Frame
The physical activity will be measured at the beginning of the study (session 0).
Title
Changes in the biomarkers: Tumor Necrosis Factor (TNF-Alpha) and Interleukin 10 (IL-10)
Description
These two cytokines are parameters to indicate the inflammation levels. Their concentrations are measured using commercial ELISA kits.
Time Frame
The concentrations of these biomarkers will be measured at the beginning (session 0) and changes will be evaluated again at the end of the treatment (session 20).

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Women aged 18 to 70 years. Diagnosis of back pain from a trauma. Untreated pain (except acetaminophen). Informed consent. Exclusion Criteria: Algic process in the lumbar spine of infectious, neoplastic, metastasis, osteoporosis, inflammatory arthritis or fractures. Cognitive impairment of any etiology. Exercise intolerance for any reason. Patients who have completed physical therapy in the last 3 months. Patients who have received infiltration injections in the last 6 weeks.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rosa Nogués, Ph D.
Phone
+34977759355
Email
mariarosa.nogues@urv.cat
First Name & Middle Initial & Last Name or Official Title & Degree
Eduard Minobes, PT
Email
eminobes@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rosa Nogués, Pharm.D.
Organizational Affiliation
Faculty of Medicine and Health Sciences. Rovira i Virgili University. Spain.
Official's Role
Study Director
Facility Information:
Facility Name
Faculty of Medicine and Health Sciences
City
Reus
State/Province
Tarragona
ZIP/Postal Code
43201
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rosa Nogués, PhD
Phone
+34977759355
Email
mariarosa.nogues@urv.cat
First Name & Middle Initial & Last Name & Degree
Eduard Minobes, PT

12. IPD Sharing Statement

Citations:
PubMed Identifier
33312766
Citation
Minobes-Molina E, Nogues MR, Giralt M, Casajuana C, de Souza DLB, Jerez-Roig J, Romeu M. Effectiveness of specific stabilization exercise compared with traditional trunk exercise in women with non-specific low back pain: a pilot randomized controlled trial. PeerJ. 2020 Nov 27;8:e10304. doi: 10.7717/peerj.10304. eCollection 2020.
Results Reference
derived

Learn more about this trial

Valuation of the Low Back Pain Treated With Different Types of Active Exercises in Women

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