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The Effect of Structured Pain Education on Pain and Performance Parameters in Patients With Chronic Low Back Pain

16 mei 2022 bijgewerkt door: Ayşe Yaşar, Medipol University

The Effect of Structured Pain Education on Pain and Performance Parameters in Patients with Chronic Low Back Pain

The aim of this study is to compare the effects of only Low Load Motor Control Exercises and Pain Education in addition to these exercises on pain, performance, disability and psychological factors, and to present a generalizable pain education in patients with chronic low back pain. We think that DYMK exercises applied together with a general Pain Education given to the patients will provide more improvement on these factors.

The patients will be divided into 2 groups, as a pain training group and an exercise group, with 20 people in each group, in a randomized controlled manner. Only DYMK exercise training will be applied to the exercise group. In the pain training group, pain training will be applied in addition to the DYMK exercise training.

As an evaluation parameter to the participants; Numerical Rating Scale, Short-Form McGill Pain Questionnaire, Pain Catastrophizing Scale, Tampa Kinesiophobia Scale, Roland-Morris Disability Questionnaire, Pain Self-Efficacy Questionnaire, Passive Lumbar Extension Test, Finger-Place Test and Physical Performance Test Battery will be applied. Patients will be evaluated before the start of the study (T0) and at the end of the study (T1).

Low Load Motor Control Exercises will be applied to people in both groups for 4 weeks, 3 days a week, during 20-30 minute sessions. In addition to the DYMK exercise training, a session of 30 to 50 minutes of Pain Training in groups of 4 to 5 people will be given to the patients included in the Pain Training group at the beginning of the exercise training and the exercise training will begin.

Studie Overzicht

Toestand

Werving

Conditie

Interventie / Behandeling

Studietype

Ingrijpend

Inschrijving (Verwacht)

35

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

  • Kalkoen
      • Istanbul, Kalkoen, 34515
        • Werving
        • Istanbul Medipol University Sefakoy Hospital
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 65 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • 18 to 65 years old
  • Chronic low back pain 3 days a week and ≥ 3 months
  • Absence of spinal fracture or acute disc herniation
  • Absence of existing psychiatric problems and mental deficiencies
  • Absence of exercise contraindications [28] [29] [30]

Exclusion Criteria:

  • Being diagnosed with lumbar radiculopathy
  • Pain due to tumors or infections, metastases, osteoporosis, inflammatory arthritis or fractures
  • Specific medical conditions (neck or back surgery in the previous 3 years, osteoporotic vertebral fractures or rheumatological diseases)
  • Chronic widespread pain syndromes (fibromyalgia or chronic fatigue syndrome)
  • Receiving any other treatment for chronic low back pain during the study [28] [29] [30]

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: exercise group
Only DYMK exercise training will be applied to the exercise group.
Ander: exercise group

1 stage

  • In a sitting position, pull the leg up and extend the knee forward
  • Standing, bending forward and bending the knee
  • Supine, tucked legs
  • Maintaining spinal smoothness in crawling
  • Prone heel pull to buttock

Stage 2

  • Prone on forearms-hands
  • Extending the supine hands to the knees
  • Rounding and hollowing the waist in crawling
  • Progressive sit-stand
  • Standing up from sitting and putting on and taking off socks
  • Reaching up while standing and maintaining the straightness of the spine
  • Squatting
  • Climbing and descending stairs

Stage 3

  • Maintaining standing, arms forward
  • Slipping hands on the bed while standing
  • Initiating the standing throw and maintaining the position until the final interval
  • Putting on and taking off socks while standing
  • Taking weight towards the ground from a certain height
  • Picking up different weights from the ground
  • Push-pull items
  • Crossing obstacles of certain height
  • Walking a certain distance
Experimenteel: pain training group
In the pain training group, pain training will be applied in addition to the DYMK exercise training.
Ander: pain training group

The training provides participants with the opportunity to explain the central sensitization mechanism and also integrates the behavioral, psychological and environmental aspects that contribute to the persistence of pain. It is intended to teach that education reduces pain and improves endogenous pain inhibition, mental health, physical function, vitality and self-rated disability in patients with chronic pain, and reduces passive coping, kinesiophobia, and catastrophizing.

The same exercises will be applied as the exercise group.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change from baseline of pain intensity on the Numerical Rating Scale at 3 weeks
Tijdsspanne: baseline and 3 weeks
It is an 11-point unidimensional measure of pain intensity. It is a segmented numerical version of the Visual Analog Scale (VAS), in which participants select an integer (0-10 integer) that best reflects the intensity of their pain. 0 represents no pain and 10 represents worst pain.
baseline and 3 weeks
Change from baseline in the multidimensional measure of pain on the Short-Form McGill Pain Questionnaire at 3 weeks
Tijdsspanne: baseline and 3 weeks
A multidimensional measure of pain. It consists of 2 subscales: 1) a sensory subscale consisting of 11 words or items, and 2) an emotional subscale consisting of 4 items rated on the intensity scale (0= none, 1= mild, 2= moderate, and 3= severe). It also includes 1 item for current pain intensity and 1 item for 10 cm Visual Analog Scale for mean pain.
baseline and 3 weeks
Change from baseline in assessing feelings, thoughts, and emotions related to pain and disaster on the Pain Catastrophizing Scale at 3 weeks
Tijdsspanne: baseline and 3 weeks
It is used to assess the patient's feelings, thoughts, and feelings about pain and disaster. It is a self-administered questionnaire with 13 items and 3 subscales: helplessness, magnification, and rumination. A 5-point scale is used for each item, with higher values representing greater destruction. The scores of each item are added to determine the subscales and the total score is calculated with the sum of all items. Scores range from 0 to 52 points.
baseline and 3 weeks
Change from baseline in measuring fear of movement and (re)injury on the Tampa Kinesiophobia Scale at 3 weeks
Tijdsspanne: baseline and 3 weeks
A 17-item questionnaire that measures fear of movement and (re)injury. Each question is answered on a 4-point Likert scale ranging from "strongly disagree" to "strongly agree". The total score is calculated after reversing the individual scores of items 4, 8, 12, and 16.
baseline and 3 weeks
Change from baseline in questioning pain-related disability from low back pain on the Roland Morris Disability Questionnaire at 3 weeks
Tijdsspanne: baseline and 3 weeks
A 24-item self-reported outcome measure questioning pain-related disability from low back pain. Items are scored 0 if left blank or 1 if approved. The total score ranges from 0 to 24; higher scores represent higher pain-related disability.
baseline and 3 weeks
Change from baseline in the patient's ability to perform a range of activities despite pain in the Pain Self-Efficacy Questionnaire at 3 weeks
Tijdsspanne: baseline and 3 weeks
A 10-item questionnaire that measures both the strength and generality of a patient's beliefs about their ability to perform a range of activities despite pain. Scores can range from 0 to 60, with higher scores indicating stronger self-efficacy beliefs.
baseline and 3 weeks
Measuring pain intensity and disability in the Revised Graded Chronic Pain Scale at baseline
Tijdsspanne: baseline
The new scale, consisting of 6 questions, was developed as a revised version of the original scale. There is a categorical rating scheme and numerical self-assessment scores for pain intensity and disability. The first 2 questions ask the frequency of pain, how the pain affects life and work activities and evaluate the last 3 months. It is scored from 0 to 4 (0 = never to 4 = every day). Questions between 3 and 5 (PEG scale) evaluate the severity of pain in the last 7 days and are scored between 0-10 points. The third question questions the severity of the pain. Questions 4 and 5, respectively, ask how pain interferes with enjoying life and how it affects general activities. Question 6 has 2 answers (1=yes and 2=no) and asks if the person is not working or unable to work because of pain or painful condition.
baseline
Change from baseline in assessing internal factors and emotions influencing the experience of health-threatening physical injury and pain in the Pain Beliefs Questionnaire at 3 weeks
Tijdsspanne: baseline and 3 weeks
The consists of two subscales. The organic beliefs subscale (PBQ-O) questions the user about physical injury or physiological pain that threaten wellness, while the psychological pain beliefs subscale (PBQ-P) evaluates intrinsic factors and emotions affecting the pain experience that may potentially threaten wellness.
baseline and 3 weeks
Identifying subjective neuropathic pain experience on the Pain Perception Questionnaire at baseline
Tijdsspanne: baseline
It is a symptom-based assessment tool performed by clinicians to specify the subjective neuropathic pain experience of patients.
baseline
Change from baseline in assessing overall quality of Sleep at 3 weeks
Tijdsspanne: baseline and 3 weeks
It's about the overall quality of sleep about most nights in the last 7 days. It is scored between 1 and 10. High scores represent good sleep quality.
baseline and 3 weeks

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change from baseline in detecting structural lumbar segmental instability on Passive Lumbar Extension Test at 3 weeks
Tijdsspanne: baseline and 3 weeks
It is a passive test that detects structural lumbar segmental instability. Participants are placed in a prone position and the physiotherapist then lifts both lower extremities simultaneously to a height of approximately 30 cm from the bed while keeping the knees extended and gently pulling the legs. The test is considered positive if the participant reports low back pain during testing.
baseline and 3 weeks
Change from baseline on trunk mobility on the Finger-Place Test at 3 weeks
Tijdsspanne: baseline and 3 weeks
It is a test that provides information about trunk mobility. The participant stands upright on a 20 cm high platform, with shoes off and feet glued together. He is asked to bend forward as much as possible, fully extending his knees, arms and fingers. The vertical distance between the tip of the middle finger and the platform is measured with a flexible tape measure and expressed in centimeters. The vertical distance between the platform and the tip of the middle finger is considered positive when the participant does not reach the platform, and negative when they can go further.
baseline and 3 weeks
Change from baseline in maintaining a neutral lumbar spine in the Physical Performance Test Battery at 3 weeks
Tijdsspanne: baseline and 3 weeks
Includes bias bridge, side bridge, Biering-Sørensen test and a motion control test battery. . All tests will be performed in standard positions. In the bias bridge, side bridge and Biering-Sørensen testing, emphasis will be placed on maintaining a neutral lumbar spine for as long as possible (seconds).
baseline and 3 weeks

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Medipol University

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

15 april 2022

Primaire voltooiing (Verwacht)

15 juni 2022

Studie voltooiing (Verwacht)

30 oktober 2022

Studieregistratiedata

Eerst ingediend

15 maart 2022

Eerst ingediend dat voldeed aan de QC-criteria

14 april 2022

Eerst geplaatst (Werkelijk)

15 april 2022

Updates van studierecords

Laatste update geplaatst (Werkelijk)

17 mei 2022

Laatste update ingediend die voldeed aan QC-criteria

16 mei 2022

Laatst geverifieerd

1 mei 2022

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • MedipolUniversity

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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