- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT04007822
Pain Navigator Tool for Self-management in Back Pain: PATiENCe Trial (PATiENCe)
Evaluation of the 'Pain Navigator Tool' During Physiotherapy Consultations in Patients With Chronic Low-back Pain: a Service Evaluation Trial.
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
Chronic pain is the largest cause of disability globally and affects up to 28 million people in the UK alone. Nearly half of those who experienced chronic pain in Europe reported receiving insufficient pain management. Conventional treatments commonly used in physiotherapy continue to show only moderate effects in pain management. A potential avenue to improve the global effect of treatments may lie in exploring non-specific treatment moderators such as the therapeutic alliance (TA). Findings suggest that it is linked with engagement in rehabilitation and is a strong predictor of treatment outcomes and adherence. This study aims to evaluate and compare the quality of practice with or without the Pain Navigator Tool (PNT). Understanding the impact of the PNT on therapeutic alliance would open an avenue to improve chronic pain management, reduce healthcare-related expenses and increase the quality of life in the population studied. In addition, exploring the experience of the physiotherapists with using the PNT will provide an in-depth understanding of its use and applicability in similar settings.
The aims of this study are to:
- To evaluate and compare the quality of practice with or without the PNT in patients with chronic low-back.
- To collect preliminary data on the usability and practicality of the PNT for physiotherapists.
Studietype
Contacten en locaties
Studie Locaties
-
-
Strathcylde
-
Glasgow, Strathcylde, Verenigd Koninkrijk, G4 0BA
- Glasgow Caledonian University
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Bemonsteringsmethode
Studie Bevolking
Physiotherapists working in an MSK outpatient clinic and are able to read and speak English to a level allowing satisfactory completion of the study procedures.
Patients with chronic low back pain attending an MSK outpatient clinic.
Beschrijving
Inclusion Criteria:
Patient:
- Participant aged >18 years
- Low-back pain for more than three months
- Able to read and speak English to a level allowing satisfactory completion of the study procedures
- Initial appointment with a participating physiotherapist
Physiotherapist:
- 2 years of experience in treating patients with chronic pain
- Currently working in an MSK outpatient clinic
- Able to read and speak English to a level allowing satisfactory completion of the study procedures
Exclusion Criteria:
Patient:
- Low-back pain is not the primary reason for physiotherapy appointment
- Return appointment with physiotherapist
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
Interventie / Behandeling |
---|---|
Physiotherapists
Physiotherapists will be recruited using the following inclusion criteria: (1) two years of experience in treating patients with chronic pain, (2) currently working in an MSK outpatient clinic and (3) able to read and speak English to a level allowing satisfactory completion of the study procedures.
There are no exclusion criterium.
Potential participants will be recruited through the relevant gatekeeper.
The gatekeeper will be responsible of forwarding the participant information sheet and consent form to the physiotherapists.
Physiotherapists will be asked to demonstrate their interest by replying to the email.
Any questions will be answered by the research team via email or phone.
|
The Pain Navigator Tool (PNT) was developed recently with the aim to empower patients through helping them to discuss their main concerns about pain, and to help therapists to prioritise addressing these concerns (Blomkvist et al., 2018).
The initial pilot study with this tool improved the content of the consultations and patient engagement, and led to better patient-therapist interaction in a small population of healthcare providers and patients (Blomkvist et al., 2018).
As it endeavours to facilitate the implementation of self-management in patients with chronic pain, the PNT aligns with the Scottish Intercollegiate Guidelines Network (SIGN) guideline for chronic pain and the Scottish Government's strategic vision (Scottish Government, 2011; SIGN, 2013).
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Semi-Structured Interview
Tijdsspanne: 4 weeks
|
Semi-structured interviews with the participating physiotherapists will explore the experience using the PNT.
|
4 weeks
|
Change in the Health Care Providers Pain and Impairment Relationship Scale
Tijdsspanne: 0 weeks, 4 weeks and at 1 month follow-up
|
The HC-PAIRS is selected to assess the pain-related attitudes and beliefs of physiotherapists.
It is a validated tool with adequate psychometric properties and has already been used in the selected population.
It measures attitudes and beliefs on a scale of 13 to 91 with higher scores on this scale indicating stronger beliefs that LBP validates disability.
|
0 weeks, 4 weeks and at 1 month follow-up
|
The Pain Self-Efficacy Questionnaire
Tijdsspanne: 4 weeks
|
The PSEQ is selected to capture the patients' levels of confidence in carrying out day-to-day tasks despite the presence of pain.
It assesses the confidence of people with any type of chronic pain in activity despite pain.
It covers enjoying activities, household daily activities, social life, coping in general, work, leisure activities, coping with pain without medication, accomplishing goals, living a normal lifestyle, and becoming more active, all 'despite pain'.
Each is rated on a 7 point scale from 0 = not at all confident to 6 = completely confident.
The total score, ranging from 0 to 60, is calculated by adding the scores for each item.
Higher scores reflect stronger self-efficacy beliefs.
|
4 weeks
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Change in the Pain Understanding and Confidence Questionnaire
Tijdsspanne: 0 weeks, 4 weeks and at 1 month follow-up
|
The PUnCQ is a two-part questionnaire assessing students' knowledge and understanding of pain alongside their confidence in applying this understanding.
The questionnaire consists of a chronic pain case vignette, with the first set of questions consisting of a 12-item multiple choice questionnaire, assessing knowledge and understanding in the context of the vignette.
The second part of the tool is a 21-item Likert scale ranging from "not at all confident" (0) to "no problem!" (10), with a higher score indicating a higher self-perceived confidence in applying this understanding.
Correct answers in the Understanding section were awarded a score of 1, and incorrect a score of 0, with a total accumulated to give a score for each participant.
|
0 weeks, 4 weeks and at 1 month follow-up
|
Medewerkers en onderzoekers
Sponsor
Medewerkers
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 260667
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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 .
Klinische onderzoeken op Pain Navigator Tool
-
National Institute of Allergy and Infectious Diseases...VoltooidVaginale infectieVerenigde Staten
-
Université de MontréalInstitut de Recherche Robert-Sauvé en Santé et en Sécurité du TravailOnbekend
-
Tolerion, Inc.Actief, niet wervendDiabetes mellitus, type 1Verenigde Staten
-
Tolerion, Inc.IngetrokkenDiabetes mellitus, type 1Verenigde Staten
-
Tolerion, Inc.IngetrokkenDiabetes mellitus, type 1
-
Cameroon Baptist Convention HealthCarolinas Medical CenterVoltooid
-
University of GlasgowScottish Universities Environmental Research CentreVoltooid
-
Stanford UniversityBeëindigdGenitale neoplasmata, vrouwelijk | Borstkanker | Gynaecologische kankersVerenigde Staten
-
Illinois Institute of TechnologyPatient-Centered Outcomes Research Institute; TrilogyVoltooidPsychische aandoeningVerenigde Staten
-
Karolinska InstitutetRegion Stockholm; Forte; Stiftelsen Frimurarna BarnhusetActief, niet wervendDepressie | Stress, psychisch | Verstandelijk gehandicapt | Ongerustheid | Neurologische ontwikkelingsstoornissen | Traumatische hersenschade | Autisme Spectrum Stoornis | Ouders | Aandachtstekortstoornis met hyperactiviteit | Fysieke handicapZweden