Chronic Low-back Pain Clinical Trial
— PATiENCeOfficial title:
Evaluation of the 'Pain Navigator Tool' During Physiotherapy Consultations in Patients With Chronic Low-back Pain: a Service Evaluation Trial.
NCT number | NCT04007822 |
Other study ID # | 260667 |
Secondary ID | |
Status | Withdrawn |
Phase | |
First received | |
Last updated | |
Start date | July 1, 2019 |
Est. completion date | March 1, 2020 |
Verified date | February 2021 |
Source | Glasgow Caledonian University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study explores the experience of physiotherapists and patients using the Pain Navigator Tool during outpatient musculoskeletal consultations.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | March 1, 2020 |
Est. primary completion date | March 1, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Glasgow Caledonian university | Glasgow | Strathcylde |
Lead Sponsor | Collaborator |
---|---|
Glasgow Caledonian University | NHS Greater Glasgow and Clyde |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Semi-Structured Interview | Semi-structured interviews with the participating physiotherapists will explore the experience using the PNT. | 4 weeks | |
Primary | Change in the Health Care Providers Pain and Impairment Relationship Scale | 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 | |
Primary | The Pain Self-Efficacy Questionnaire | 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 | |
Secondary | Change in the Pain Understanding and Confidence Questionnaire | 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 |
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