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Chronic Nonspecific Low Back PainNCT03181659

Therapeutic Exercise and Therapeutic Patient Education With or Without Manual Therapy for Chronic Nonspecific Low Back Pain.

A study testing Manual Therapy, Therapeutic Education, Therapeutic Exercice and Therapeutic Education, Therapeutic Exercice in people with Chronic Nonspecific Low Back Pain and Low Back Pain, run by Roy La Touche Arbizu at 1 site in Spain.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This clinical trial study evaluates the effectiveness of a multimodal physiotherapy treatment based on a biobehavioural paradigm in the treatment of non-specific chronic low back pain. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Manual Therapy, Therapeutic Education, Therapeutic Exercice and Therapeutic Education, Therapeutic Exercice
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
88 participants
Where
1 siteSpain
Study dates
1 Sep 2017to 30 May 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients with non specific low back pain lasting for at least 3 months.
  • Patients with pain intensity corresponding to at least 3 points on a 10 point analogue visual scale.
  • Patients with pain frequency corresponding to at least 10 days per month.
  • Men and Women between 18 and 65 years old.

Who cannot join

  • Presence of trauma or surgery to the thoracic or lumbar region.
  • Patients with diagnosis of discopathy or radicular symptoms.
  • Patients with history of previous physical-therapy intervention for the lumbar region in the last month.
  • Any cognitive impairment that hindered viewing of audiovisual material.
  • difficulty understanding or communicating.
  • Presence of systemic pathology, Central Nervous System or rheumatic disease.
  • Inadequate understanding of the Spanish language to follow instructions for measuring and treatment.
  • Collaboration of pregnant women.

Trial locations and contacts

1 site in 1 country.

Roy A La Touche, physiotherapist contact

917401980 ext. 313

roylatouche@lasallecampus.es

Mónica A Grande, physiotherapist contact

660638251

monica.grande@irflasalle.es

Spain1 site, 1 recruiting

  • CSEU La Salle

    Madrid, 28023

    Roy A A La Touche, physiotherapist, 917401980 ext. 313, roylatouche@lasallecampus.es

    Mónica M Grande, physiotherapist, 660638251, monica.grande@irflasalle.es

    Recruiting

Other trials in Spain

About this study

Official title: Therapeutic Exercise and Therapeutic Patient Education With or Without Manual Therapy for Chronic Nonspecific Low Back Pain: a Randomized Control Trial.

This clinical trial study evaluates the effectiveness of a multimodal physiotherapy treatment based on a biobehavioural paradigm in the treatment of non-specific chronic low back pain. The experimental group received treatment based on therapeutic exercise, education in neuroscience, and manual therapy, contrary to the control group, which did not receive manual therapy treatment.

Read the detailed description

Low back Pain (LBP) is defined by patients as a pain located between the low margins of the costal gridiron and the top limits of the buttock musculature, and it can either be of short or long duration. LBP is the most prevalent musculoskeletal problem, assuming a prevalence between 18,6% and 57,4%. Traditionally, the diagnosis of the DL continues to be based on pathoanatomical criteria even though, in numerous occasions, the outcomes found in complementary tests of image do not correlate with the intensity of pain and the level of disability of the patients. According to the guides of clinical practice, LBP can be divided in three subgroups: firstly, patients whose pain can be associated to a previous pathology, secondly, patients with a diagnosed neuropathic pain associated to a neurological condition, and lastly, patients who present LBP of unspecific characteristics, not preceded by any pathology or relevant damage. According to the World Health Organization, the latter represent 90% of the cases. Thus, this problem supposes a high index of chronicity, and it is the principal reason of labor absenteeism and disability encountered in society, as well as one of the most common motives of consultation in centers of primary care and specialized attention, which results in a high socioeconomic cost. As for the intervention of the CLBP, nowadays there are numerous studies based on disabling the processing of central and peripheral levels of pain by means of a multidisciplinary boarding based on psychology and on a biobehavioral approach. The aim of this study is to evaluate the efficiency of a multimodal treatment by means of therapeutic exercise (TE) and education in neuroscience (NE), with or without manual therapy (MT).

TE is one of the most frequently used techniques, and one of the most effective in patients with CLBP. Research shows reduction of pain in healthy people through either aerobic exercise, resistance exercise, or isometric exercise, showing an increase in pain thresholds and pain intensity. NE aims to change maladaptive beliefs and erroneous thoughts that interfere in the perception of pain and which lead to increase the presence of psychological variables such as fear of movement, hypervigilance, and catastrophism, enhancing the perpetuation and chronicity of the same. Additionally, MT offers a wide range of specific techniques for the treatment of musculoskeletal disorders with the aim of obtaining a modulation of pain through the neurophysiological effects produced at both peripheral and central levels.

The hypothesis of the present study is that TE, when combined with both NE and MT, is more effective on the principal variables of study after 3 months of follow-up. It is a clinical trial randomized with masking of the assessor. An evaluation of the variables previously described will take place, and it will be measured by a trained physical therapist before receiving the treatment. The second evaluation will be conducted after finishing the intervention, whereas a last evaluation will be undertaken after 3 months of follow-up. The intervention will be carried out by a specialized physical therapist that will use a multimodal approach in a simple, randomized way by means of the software known as GraphPad, which allows us to randomly divide the participants into two groups. The group control will receive a treatment based on a total of 8 sessions, at a rate of 2 sessions per week. In total, a number of 4 sessions of NE will take place once per week during a period of four weeks, together with 7 TE sessions. The experimental group will receive the same intervention that the control group in combination with TM based on a protocol, which will develop during a period of 20-25 minutes, 2 sessions per week, in a total of 8 sessions. Groups will have to continue receiving NE and, regularly, they will receive a total of 4 follow-ups on the process of education via audio-visual material.

Being tested
Manual Therapy, Therapeutic Education, Therapeutic Exercice, Therapeutic Education, Therapeutic Exercice
Keywords
Musculoskeletal Manipulations, Exercise, Patient Education, Low back pain
Medical subject headings
Low Back Pain, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Manual Therapy, Therapeutic Education, Therapeutic ExerciceProcedure or surgery

    They will receive 8 sessions (2 sessions per week) of joint and neural manual therapy, and will receive 4 sessions (1 session per week) of neuroscience education in which mirror therapy and image observation. The therapeutic exercise program is based on stabilization of the lumbopelvic region.

  • Therapeutic Education, Therapeutic ExerciceProcedure or surgery

    They will receive a total of 8 sessions (2 sessions per week) of therapeutic exercise based on the stabilization of the lumbopelvic region and will receive 4 sessions (1 session per week) of neuroscience education in which mirror therapy and image observation.

Study groups in NCT03181659
Study groupRoleWhat they receive
Group 1: patients with NSCLBP who do not seek careExperimentalManual Therapy, Therapeutic Education, Therapeutic Exercice
Receives: Procedure: Manual Therapy, Therapeutic Education, Therapeutic Exercice
Group 2: patients with NSCLBP who do not seek careExperimentalTherapeutic Education, Therapeutic Exercice
Receives: Procedure: Therapeutic Education, Therapeutic Exercice
Group 3: patients with NSCLBP who seek careExperimentalManual Therapy, Therapeutic Education, Therapeutic Exercice
Receives: Procedure: Manual Therapy, Therapeutic Education, Therapeutic Exercice
Group 4: patients with NSCLBP who seek careExperimentalTherapeutic Education, Therapeutic Exercice
Receives: Procedure: Therapeutic Education, Therapeutic Exercice

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Disability and function

    The Roland Morris Disability Questionnaire (RMDQ) will be used to assess the physical disability in activities of daily living due to low back pain. This self-administered questionnaire consists of 24 items that refer to the limitations of daily activities as a result of low back pain (Roland and Morris, 1983). The total score ranges from 0 to 24 (higher scores indicate a more severe disability level). The Spanish version of RMDQ has been demonstrated as having acceptable psychometric properties (Kovacs et al., 2002).

    Measured: Change from disability and function at 3 months.

  2. Pain Intensity

    Pain Intensity will be measured with Visual Analogue Scale (VAS). The VAS consists of a 100-mm line, the left side of which represents "no pain" whereas the right side represents "maximal pain" (Bijur et al., 2001).

    Measured: Change from pain intensity at 3 months.

  3. Isometric Force Endurance

    To evaluate the force endurance of the lumbar stabilizing muscles, the Ito test is used to test isometric isometric elevation of the trunk (Moreau et al., 2001). This assay was described by Ito et al. 1996 and has a good level of reliability (Ito et al., 1996). In this test the subject will be asked to lie prone on the stretcher. Then, the subject must elevate his head and trunk of the stretcher, in the way that his sternum does not come into contact with it, maintaining the maximum possible cervical flexion. The subjects must maintain this position in the longest possible time, finishing the test after 5 minutes, a state of fatigue or pain appears.

    Measured: Change from Isometric force endurance at 3 months.

Secondary outcomes (11)

  1. Temporal Summation

    The temporal summation of stimuli will be measured by Von Frey filaments on the area of worst pain in the lumbar region and on the forearm of the non-dominant upper limb as the control area.; At first a single stimulus will be performed on these points, applied for 0.5 seconds, and then the patient will assess the intensity of pain through a VAS scale. Subsequently, on the same points, 10 rhythmic stimuli will be performed at 1-second intervals and again the intensity of pain will be assessed by a VAS (Starkweather et al., 2015).

    Measured: Temporal Summation will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  2. Two-point discrimination

    The discrimination of two points was evaluated both on the healthy side and on the affected side through an ossiometer, which is accountable for measuring the tactile sensitivity. It consists of a small ruler with two mobile tips. During the test the patient was asked to close his eyes while the Physiotherapist produced tactile stimuli through the instrument and the patient indicated whether he felt one or two contacts. Finally, the smallest distance in millimetres recognized by the patient was measured (Catley et al., 2013).

    Measured: Two-Point discrimination will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  3. Funcional range

    The functional range test was developed by Duncan as a predictor of falls in adulthood (Duncan et al., 1990). It is a measure of postural stability from the multi-directional reach of the upper limb with a fixed base. The functional use test was first validated for the former and subsequently for adults obtaining a good reliability of the measurement of stability (Newton et al.,2001) For the calculation of this test, use a measuring device consisting of a tripod containing a rigid tape measure, parallel to the ground, and placed at the height of the acromion of each subject with elbows and hands in complete extension. The subject has to reach as far as possible maintaining the posture for 2-3 seconds without lifting the feet off the ground.

    Measured: Funcional range will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  4. Strength of lumbar region

    The strength of the lumbar region will be measured by a foot dynamometer (Takei TM 5420). The patient should stand on the dynamometer platform with knees extended, elbows extended, hips bent and index fingers holding the bar at knee height. Starting from this position the subject will have to make a previous adjustment of contraction of the musculature of the lumbar region and must perform a movement of lumbar extension. Subjects should maintain contraction for 3 seconds. It is a valid and reliable test to measure the muscular strength of the lumbar region (Coldwells et al.,1994)

    Measured: Strength of the lumbar region will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  5. Motor control of lumbar region

    Lumbar motor control will be measured by a pressure biofeedback called Stabilizer TM. The measurement protocol in the following procedure; The patient should be supine position with the Stabilizer TM placed in the lumbar region with an initial pressure of 70 mmHg. Then, the patient will be asked to flex the hip and knee at 90 ° with one leg and then with the opposite one repeating the procedure 3 times, then performing a total average. It is a validated and reliable protocol for motor control of the lumbar region (Azevedo et al., 2013)

    Measured: Motor control will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  6. Range of movement

    The range of lumbar movement will be measured using a digitized inclinometer based on a mobile application called iHandy ®. Such an application provides the ability to convert the mobile device into an inclinometer. The inclinometer has proven to be a valid and reliable instrument for measuring lumbar range of motion (Saur et al., 1996) The measurement protocol consists of the following process: the patient should stand in a standing position with the arms along the body. The evaluating physiotherapist will mark the T12 level at the height of the last rib and later the L4-L5 level using the iliac crest as the anatomical reference. There will be 5 movements; Thoraco-lumbar flexion, lumbar flexion, thoraco-lumbar extension, right lateral thoraco-lumbar flexion and left lateral thoraco-lumbar flexion (Kolber et al., 2013)

    Measured: Range of movement will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  7. Dynamic Stability

    Dynamic stability will be assesed with Y-Balance test. It is a reliable clinical test of that evaluates the neuromuscular control of the trunk and the lower limbs (Pilsky et al.2009). The subject is in the center of a three-arm platform, which has one arm in the anterior direction, and two in the posterior direction, one medial and one lateral with a 45º separation between them and 135º with respect to the anterior arm. Each arm has a graphic scale in length measurements for distance measurement. The arm contains a scope aiming objective that the subject will have to slide along the arm to accurately measure how far they can reach with one lower limb while the other is in the center of the platform. Once the maximum possible distance has been reached the subject must pick up his lower limb back to the platform without resting it on the ground. The upper limbs will be supported like a pitcher on the hips

    Measured: Dynamic Stability will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  8. Pain catastrophizing

    The Spanish version of the pain catastrophizing scale (PCS) assesses the degree of pain catastrophizing. The PCS has 13 items and a 3-factor structure of rumination, magnification, and helplessness (García Campayo J et al., 2008)

    Measured: Pain catastrophizing will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  9. Kinesiophobia

    Fear of movement or kinesiophobia will be quantified with the Spanish version of the Kinesiophobia Tampa Scale (TSK-11). This instrument demonstrates reliability and validity in patients with chronic pain, being shorter than the original scale. The total score ranges from 11 to 44 points, with the highest scores indicating greater fear of a new injury due to movement (Gómez-Pérez L et al., 2011)

    Measured: Kinesiophobia will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  10. Self-efficacy

    Self-efficacy will be evaluated through the short version of the General Self-Efficacy Scale, which evaluates initiative, persistence, and effort. It is a scale validated in Spanish and has demonstrated validity, reliability and good internal consistency (Herrero et al., 2014)

    Measured: Self-efficacy will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

  11. Anxiety and Depression

    Anxiety and Depression will be evaluated through The Spanish version of the Anxiety and Depression Scale (HADS) is a 14-item instrument with a 4-item Likert scale that measures from 0 to 3. This instrument has two subscales consisting of 7 items each (Perez et al.,1995)

    Measured: Anxiety and Depression will be assessed up to 1 week before treatment, up to 1 week after treatment and after 3 months of follow up.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Jun 2017
  2. Study start1 Sep 2017
  3. Primary completion29 Dec 2018 (estimated)
  4. Study completion30 May 2019 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
88 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03181659
Sponsor's protocol ID
1
Status last verified
Sep 2018
First submitted
9 May 2017
Last updated
6 Sep 2018
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Roland M, Morris R. A study of the natural history of back pain. Part I: development of a reliable and sensitive measure of disability in low-back pain. Spine (Phila Pa 1976). 1983 Mar;8(2):141-4. doi: 10.1097/00007632-198303000-00004. No abstract available.

    PubMed 6222486

  • Kovacs FM, Llobera J, Gil Del Real MT, Abraira V, Gestoso M, Fernandez C, Primaria Group KA. Validation of the spanish version of the Roland-Morris questionnaire. Spine (Phila Pa 1976). 2002 Mar 1;27(5):538-42. doi: 10.1097/00007632-200203010-00016.

    PubMed 11880841

  • Bijur PE, Silver W, Gallagher EJ. Reliability of the visual analog scale for measurement of acute pain. Acad Emerg Med. 2001 Dec;8(12):1153-7. doi: 10.1111/j.1553-2712.2001.tb01132.x.

    PubMed 11733293

  • Moreau CE, Green BN, Johnson CD, Moreau SR. Isometric back extension endurance tests: a review of the literature. J Manipulative Physiol Ther. 2001 Feb;24(2):110-22. doi: 10.1067/mmt.2001.112563.

    PubMed 11208223

  • Ito T, Shirado O, Suzuki H, Takahashi M, Kaneda K, Strax TE. Lumbar trunk muscle endurance testing: an inexpensive alternative to a machine for evaluation. Arch Phys Med Rehabil. 1996 Jan;77(1):75-9. doi: 10.1016/s0003-9993(96)90224-5.

    PubMed 8554479

  • Starkweather AR, Heineman A, Storey S, Rubia G, Lyon DE, Greenspan J, Dorsey SG. Methods to measure peripheral and central sensitization using quantitative sensory testing: A focus on individuals with low back pain. Appl Nurs Res. 2016 Feb;29:237-41. doi: 10.1016/j.apnr.2015.03.013. Epub 2015 Apr 8.

    PubMed 26856520

  • Catley MJ, Tabor A, Wand BM, Moseley GL. Assessing tactile acuity in rheumatology and musculoskeletal medicine--how reliable are two-point discrimination tests at the neck, hand, back and foot? Rheumatology (Oxford). 2013 Aug;52(8):1454-61. doi: 10.1093/rheumatology/ket140. Epub 2013 Apr 22.

    PubMed 23611918

  • Duncan PW, Weiner DK, Chandler J, Studenski S. Functional reach: a new clinical measure of balance. J Gerontol. 1990 Nov;45(6):M192-7. doi: 10.1093/geronj/45.6.m192.

    PubMed 2229941

  • Newton RA. Validity of the multi-directional reach test: a practical measure for limits of stability in older adults. J Gerontol A Biol Sci Med Sci. 2001 Apr;56(4):M248-52. doi: 10.1093/gerona/56.4.m248.

    PubMed 11283199

  • Coldwells A, Atkinson G, Reilly T. Sources of variation in back and leg dynamometry. Ergonomics. 1994 Jan;37(1):79-86. doi: 10.1080/00140139408963625.

    PubMed 8112285

  • Azevedo DC, Lauria AC, Pereira AR, Andrade GT, Ferreira ML, Ferreira PH, Van Dillen L. Intraexaminer and interexaminer reliability of pressure biofeedback unit for assessing lumbopelvic stability during 6 lower limb movement tests. J Manipulative Physiol Ther. 2013 Jan;36(1):33-43. doi: 10.1016/j.jmpt.2012.12.008.

    PubMed 23380212

  • Saur PM, Ensink FB, Frese K, Seeger D, Hildebrandt J. Lumbar range of motion: reliability and validity of the inclinometer technique in the clinical measurement of trunk flexibility. Spine (Phila Pa 1976). 1996 Jun 1;21(11):1332-8. doi: 10.1097/00007632-199606010-00011.

    PubMed 8725925

  • Kolber MJ, Pizzini M, Robinson A, Yanez D, Hanney WJ. The reliability and concurrent validity of measurements used to quantify lumbar spine mobility: an analysis of an iphone(R) application and gravity based inclinometry. Int J Sports Phys Ther. 2013 Apr;8(2):129-37.

    PubMed 23593551

  • Plisky PJ, Gorman PP, Butler RJ, Kiesel KB, Underwood FB, Elkins B. The reliability of an instrumented device for measuring components of the star excursion balance test. N Am J Sports Phys Ther. 2009 May;4(2):92-9.

    PubMed 21509114

  • Garcia Campayo J, Rodero B, Alda M, Sobradiel N, Montero J, Moreno S. [Validation of the Spanish version of the Pain Catastrophizing Scale in fibromyalgia]. Med Clin (Barc). 2008 Oct 18;131(13):487-92. doi: 10.1157/13127277. Spanish.

    PubMed 19007576

Questions about this trial

What is this clinical trial studying?

A study testing Manual Therapy, Therapeutic Education, Therapeutic Exercice and Therapeutic Education, Therapeutic Exercice in people with Chronic Nonspecific Low Back Pain and Low Back Pain, run by Roy La Touche Arbizu at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 6 Sep 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Roy A La Touche, physiotherapist (917401980 ext. 313, roylatouche@lasallecampus.es), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Disability and function (time frame: Change from disability and function at 3 months.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03181659, which also lists 17 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Sep 2018.

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