Biopsychosocial Exploration of Pain Profiles in Inflammatory and Chronic Non-specific Axial Low Back Pain
19. oktober 2016 opdateret af: Lolwah Al-Rashed, University of Dublin, Trinity College
Biopsychosocial Exploration of Pain Profiles in Inflammatory and Chronic Non-specific Axial Low Back Pain: An Exploration of Similarities and Differences
The biopsychosocial model is well established in chronic low back pain (CLBP) research.
Nevertheless, researchers to date have overlooked the biopsychosocial aspects of Inflammatory Low Back pain (ILBP).
Most health care providers are biologically oriented in their treatment of ILBP, neglecting its possible multidimensional nature.
It is true that people with ILBP may present with more complex pain and physical limitations than those with chronic non-specific low back pain (CNSLBP), but it remains unexplored whether or not these limitations are affected by the same pain factors that affect CNSLBP patients.
This study aims to explore and compare the biopsychosocial back pain profiles of adults with ILBP and CNSLBP.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
This is a multicentre case-control study that will compare back pain in patients with ankylosing spondylitis and CNSLBP.
A multidimensional pain assessment will be conducted for patients in both groups.
Each patient will be assessed on one occasion by the same experienced physiotherapist.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
58
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Dublin, Irland, D24
- Physiotherapy Department, Adelaide and Meath Incorporating the National Children's Hospital (Tallaght Hospital)
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Dublin, Irland, D8
- Ankylosing Spondylitis clinic, Rheumatology Department, St. James's Hospital
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Dublin, Irland, D8
- Physiotherapy Department, St. James's Hospital
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
A convenience sample of adults with Ankylosing Spondylitis (AS) will be consecutively recruited from a pool of patients referred to AS clinic in the Rheumatology and Physiotherapy Departments of St. James's and Tallaght Hospitals in Dublin.
Adults with chronic non-specifi low back pain (CNSLBP) (control group) will be consecutively recruited from a pool of patients referred to the Physiotherapy Department of St. James's and Tallaght Hospitals in Dublin. An invitation to participate in the study and an information leaflet will be extended to the patients who potentially meet the recruitment criteria.
Beskrivelse
Inclusion Criteria:
- Adult between 18 and 65 years of age
- Low back pain >3 months
- On stable medication
- Ability to walk independently without an assistive device
- Specific inclusion criteria for AS group: clinical diagnosis of ankylosing spondylitis by a rheumatologist
- Specific inclusion for CNSLBP group: clinical diagnosis by a physician for CLBP
Exclusion Criteria:
- Spinal surgery or compression fracture within the last 6 months
- Cauda equine and conus medullaris syndromes
- Severe musculoskeletal conditions affecting the upper and/or the lower limbs, such as severe inflammatory arthritis of the peripheral joints
- Severe osteoporosis
- Leg-length discrepancy
- Cancer
- Morbid obesity, or pregnancy
- Progressive neurological disease
- Psychiatric disease and/or cognitive limitations that could affect the ability to complete the study questionnaires
- Inability to read and/or understand the English language
- Severe cardiac, respiratory or neurological diseases
- Uncontrolled epilepsy
- Specific exclusion criteria for CNSLBP group: Spondyloarthropathy, or any structural abnormalities in the lumbar spine that result in serious neurological dysfunction, such as stage III-IV lumbar disc herniation, and grade III-IV spondylolisthesis
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
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Ankyloserende spondylitis
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Chronic non-specific low back pain
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Back pain intensity - total
Tidsramme: Day 1, no follow-up will be required.
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The average total back pain intensity in the last week will be measured by the Numeric Rating Scale (NRS)
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Day 1, no follow-up will be required.
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Back pain-related functional disability
Tidsramme: Day 1, no follow-up will be required.
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Oswestry Disability Index (ODI)
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Day 1, no follow-up will be required.
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Back pain beliefs
Tidsramme: Day 1, no follow-up will be required.
|
Back Beliefs Questionnaire (BBQ)
|
Day 1, no follow-up will be required.
|
|
Pain-related fear, fear of movement/(re)injury
Tidsramme: Day 1, no follow-up will be required.
|
Tampa Scale for Kinesiophobia (TSK)
|
Day 1, no follow-up will be required.
|
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The fear-avoidance behaviours of physical activity
Tidsramme: Day 1, no follow-up will be required.
|
modified Fear Avoidance Behaviour Questionnaire (mFABQ)
|
Day 1, no follow-up will be required.
|
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Pain catastrophizing behavior
Tidsramme: Day 1, no follow-up will be required.
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Pain catastrophizing scale (PCS)
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Day 1, no follow-up will be required.
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Self-efficacy for AS patients
Tidsramme: Day 1, no follow-up will be required.
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Ankylosing Spondylitis-specific Arthritis Self-Efficacy Scale (ASES-AS)
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Day 1, no follow-up will be required.
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Pain cognition and coping
Tidsramme: Day 1, no follow-up will be required.
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Pain Coping Inventory (PCI)
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Day 1, no follow-up will be required.
|
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Psychological distress (depression & anxiety)
Tidsramme: Day 1, no follow-up will be required.
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Hospital Anxiety and Depression Scale (HADS)
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Day 1, no follow-up will be required.
|
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The extent and location of pain
Tidsramme: Day 1, no follow-up will be required.
|
Pain drawings will be completed for NSCLBP patients on a digital tablet (iPad 2, Apple Computer, Cupertino, CA, USA) using a commercially available sketching software (SketchBook)
|
Day 1, no follow-up will be required.
|
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Back pain intensity - nocturnal
Tidsramme: Day 1, no follow-up will be required.
|
The average nocturnal back pain intensity in the last week will be measured by the Numeric Rating Scale (NRS)
|
Day 1, no follow-up will be required.
|
|
Physical function for AS patients
Tidsramme: Day 1, no follow-up will be required.
|
Bath Ankylosing Spondylitis Functional Index (BASFI)
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Day 1, no follow-up will be required.
|
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Disease activity for AS patients
Tidsramme: Day 1, no follow-up will be required.
|
Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)
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Day 1, no follow-up will be required.
|
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Disease activity for AS patients
Tidsramme: Day 1, no follow-up will be required.
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Ankylosing Spondylitis Disease Activity Score (ASDAS)
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Day 1, no follow-up will be required.
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Global well-being for AS patients
Tidsramme: Day 1, no follow-up will be required.
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Bath Ankylosing Spondylitis Global score (BAS-G)
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Day 1, no follow-up will be required.
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Flexibility and spinal mobility for AS patients
Tidsramme: Day 1, no follow-up will be required.
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Bath Ankylosing Spondylitis Metrology Index (BASMI)
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Day 1, no follow-up will be required.
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Chest expansion
Tidsramme: Day 1, no follow-up will be required.
|
Chest expansion will be measured circumferentially using a tape measure
|
Day 1, no follow-up will be required.
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Forward bending
Tidsramme: Day 1, no follow-up will be required.
|
Finger-to-Floor Distance in centimetres (cm) will be measured using a tape measure
|
Day 1, no follow-up will be required.
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Isometric endurance of the trunk extensor muscles
Tidsramme: Day 1, no follow-up will be required.
|
Ito test
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Day 1, no follow-up will be required.
|
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Isometric endurance of the the trunk flexor muscles
Tidsramme: Day 1, no follow-up will be required.
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Shirado test
|
Day 1, no follow-up will be required.
|
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Grip strength
Tidsramme: Day 1, no follow-up will be required.
|
Hand grip dynamometer (Jamar Hydraulic Hand Dynamometer)
|
Day 1, no follow-up will be required.
|
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Functional performance
Tidsramme: Day 1, no follow-up will be required.
|
50-foot walk test
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Day 1, no follow-up will be required.
|
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Functional performance and endurance
Tidsramme: Day 1, no follow-up will be required.
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6-min walk distance (6MWD) test
|
Day 1, no follow-up will be required.
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Fiona Wilson, Trinity College Dublin, Ireland
- Ledende efterforsker: Lolwah A Al-Rashed, Trinity College Dublin, Ireland
- Ledende efterforsker: Finbar O'Shea, St. James's Hospital, Dublin, Ireland
- Ledende efterforsker: Deborah Falla, University Medical Center Göttingen, Georg-August University, Göttingen, Germany
- Ledende efterforsker: Marco Barbero, University of Applied Sciences and Arts of Southern Switzerland (SUPSI), Manno, Switzerland
- Ledende efterforsker: Aisling Brenan, Adelaide and Meath Hospital Dublin incorporating the National Children's Hospital (Tallaght Hospital), Dublin, Ireland
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. september 2015
Primær færdiggørelse (Faktiske)
1. august 2016
Studieafslutning (Faktiske)
1. august 2016
Datoer for studieregistrering
Først indsendt
27. februar 2016
Først indsendt, der opfyldte QC-kriterier
4. marts 2016
Først opslået (Skøn)
10. marts 2016
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
21. oktober 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. oktober 2016
Sidst verificeret
1. oktober 2016
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- UDublinTC 12
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