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Simple and Evidence-based Examination and Treatment of Shoulder Pain in General Practice (EASIER)

Primary Purpose

Shoulder Pain, Frozen Shoulder, Rotator Cuff Tendinosis

Status
Recruiting
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Evidence based treatment strategy
Targeted patient information package
Treatment as usual (TAU)
Sponsored by
University of Oslo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Shoulder Pain focused on measuring General practice, Implementation, Guideline

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Pain in the shoulder region
  • Above 18 years

Exclusion Criteria:

  • Unable to fill in self-report questionnaires or do not understand Norwegian
  • Acute injury with clinical suspicion of fracture, luxation of shoulder joints or large tendon ruptures
  • Clinical suspicion of referred pain to the shoulder area from other organs
  • Signs of inflammatory joint disease
  • Suspicion of malignant disease
  • Symptoms and signs of cervical radiculopathy

Sites / Locations

  • Department of Research and innovation, Helse Fonna, NorwayRecruiting
  • Department of General Practice, University of OsloRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intervention

Treatment as usual (TAU)

Arm Description

Patients will be assessed by GPs who have attended an outreach workshop and trained at using an evidence based strategy for shoulder examination and treatment. GPs will have access to a decision support tool and patients is offered a tailored information package for self management.

The participants enrolled in the control period will receive treatment as offered in general practice.

Outcomes

Primary Outcome Measures

Change in Shoulder Pain and Disability Index (SPADI)
13 item patient reported questionnaire on shoulder pain and disability. (0 = no pain or shoulder disability, 100 = worst pain and disability).

Secondary Outcome Measures

the EuroQol quality of life measure (EQ5D-5L)
Health related quality of life ((0 (death) - 1.0 (perfect health))
Patient reported quality of care index (treatment according to the guideline intervention)
Patient reported content of treatment measured on six items according to treatment prescribed by the GP measured on 5-item Likert scales. Sum score above 18 points regarded as consultation of high quality according to guideline intervention.
Global patient perceived effect of treatment outcome (GPE)
1 item (7-point) ( 0 = worse than ever, 7 =I have become completely well)

Full Information

First Posted
March 3, 2021
Last Updated
November 1, 2022
Sponsor
University of Oslo
Collaborators
Helse Fonna
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1. Study Identification

Unique Protocol Identification Number
NCT04806191
Brief Title
Simple and Evidence-based Examination and Treatment of Shoulder Pain in General Practice
Acronym
EASIER
Official Title
Making Shoulder Pain Simple in General Practice-implementing an Evidenced Based Guideline for Shoulder Pain, a Hybrid Design Cluster Randomised Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 11, 2021 (Actual)
Primary Completion Date
May 30, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Oslo
Collaborators
Helse Fonna

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Previous research suggests that general practitioners find handling patients with shoulder pain difficult and that the current care for shoulder pain is not in line with the best available evidence (1).This project aims to assess the effectiveness, costs and implementation of an evidence-based guideline for shoulder pain in general practice.
Detailed Description
A simplified and evidence-based algorithm for examination and treatment of patients with shoulder pain will be developed and implemented in general practice. The purpose is to improve quality of care and provide GPs with a simplified and efficient tool to handle patients with common shoulder- related pain. The study is a stepped-wedge, cluster-randomized trial with a hybrid design including a effectiveness, cost and implementation assessment of a guideline-based intervention in clinical practice (2). General practitioners in Norway will be recruited and the GP offices will be randomized to the time of crossover from current treatment as usual (TAU) to the implementation of the intervention. The intervention is a tailored strategy that includes workshops for general practitioners covering information and access to a decision support tool, an education program where the general practitioner learn an evidence-based approach to shoulder pain and access to patient information materials. Outcomes will be measured at patient and GP levels, using self-report questionnaires, focus group interviews and register based data.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Shoulder Pain, Frozen Shoulder, Rotator Cuff Tendinosis, Myalgia, Rotator Cuff Impingement Syndrome, Rotator Cuff Tear or Rupture, Not Specified as Traumatic
Keywords
General practice, Implementation, Guideline

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Stepped wedge randomized study
Masking
Outcomes Assessor
Masking Description
Outcome assessor will be blinded for treatment allocation. Randomization will be done after recruitment of GPs. GPs and study coordinators and outcome evaluators will be blinded to the allocation sequence with only the allocation of the next GP surgery being revealed by randomization list holder approximately 6 weeks before each intervention implementation point.
Allocation
Randomized
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Patients will be assessed by GPs who have attended an outreach workshop and trained at using an evidence based strategy for shoulder examination and treatment. GPs will have access to a decision support tool and patients is offered a tailored information package for self management.
Arm Title
Treatment as usual (TAU)
Arm Type
Active Comparator
Arm Description
The participants enrolled in the control period will receive treatment as offered in general practice.
Intervention Type
Other
Intervention Name(s)
Evidence based treatment strategy
Intervention Description
Evidence-based clinical examination and treatment plan
Intervention Type
Other
Intervention Name(s)
Targeted patient information package
Intervention Description
GPs will in cooperation with the patients tailor a information package targeted to the patients needs regarding their clinical shoulder diagnosis and individual implications and needs (Pain, sleep, exercises etc.).
Intervention Type
Other
Intervention Name(s)
Treatment as usual (TAU)
Intervention Description
Usual care as provided by the GP
Primary Outcome Measure Information:
Title
Change in Shoulder Pain and Disability Index (SPADI)
Description
13 item patient reported questionnaire on shoulder pain and disability. (0 = no pain or shoulder disability, 100 = worst pain and disability).
Time Frame
Change from 0 to 12 weeks
Secondary Outcome Measure Information:
Title
the EuroQol quality of life measure (EQ5D-5L)
Description
Health related quality of life ((0 (death) - 1.0 (perfect health))
Time Frame
Change from 0 weeks to 52 weeks
Title
Patient reported quality of care index (treatment according to the guideline intervention)
Description
Patient reported content of treatment measured on six items according to treatment prescribed by the GP measured on 5-item Likert scales. Sum score above 18 points regarded as consultation of high quality according to guideline intervention.
Time Frame
0 week (after 1. visit to general practitioner)
Title
Global patient perceived effect of treatment outcome (GPE)
Description
1 item (7-point) ( 0 = worse than ever, 7 =I have become completely well)
Time Frame
Measured at 6,12 and 52 weeks. Primary analysis of interest is at 12 weeks.
Other Pre-specified Outcome Measures:
Title
Brief illness perception questionnaire (BIPQ)
Description
Illness perception 0-80 where a higher score reflects a more threatening view of the illness
Time Frame
Measured at 0, 6, 12, 52 weeks, Primary time point of interest is 12 weeks and analysing changescore from 0 to 12 weeks.
Title
Pain self-efficacy questionnaire (PSEQ)
Description
Self efficacy for pain 0-60 where higher score reflects higher self efficacy for pain.
Time Frame
Measured at 0, 6, 12, 52 weeks, primary time point of interest is 12 weeks analysing change score from 0 to 12 weeks.
Title
Work disability patient reported
Description
Sick leave reported as whole days away from work
Time Frame
Measured at 0, 6, 12, 52 weeks
Title
Örebro Musculoskeletal Pain Screening Questionnaire (Short)
Description
Psychosocial, prognostic factors for musculoskeletal pain. The total score will range between 1 and 100, with a score >50 indicating higher estimated risk for future work disability
Time Frame
Measured at 0 weeks
Title
Pateint reported frequency of therapy due to shoulder pain in primary and secondary health care
Description
Reported number of consultations by GPs, specialists (orthopeds, rheumatologists, physiatrists or neurologists), physiotherapists, chiropractists and alternative therapists, injections and surgery.
Time Frame
Measured at 0, 6, 12, 52 weeks
Title
Patient reported frequency of use of supplemental investigations in primary and secondary health care.
Description
Number of investigations; blood tests and radiology (Projectional radiograph, CT, MRI)
Time Frame
Measured at 0, 6, 12, 52 weeks
Title
Patient reported direct economical expences due to shoulder pain
Description
Patient reported use of medication reported as type of medication and frequency last week
Time Frame
Measured at 0, 6, 12, 52 weeks
Title
Patient reported indirect economical expences due to shoulder pain; travel distance to therapy
Description
Patient reported travel distance to therapy measured in km
Time Frame
Measured at 0, 6, 12, 52 weeks
Title
Patient reported indirect economical expences due to shoulder pain; time away for therapy measured in hours
Description
Patient reported time away for therapy measured in hours
Time Frame
Measured at 0, 6, 12, 52 weeks
Title
Patient reported indirect economical expences due to shoulder pain; time away for work measured in hours.
Description
Patient reported time away from work measured in hours
Time Frame
Measured at 0, 6, 12, 52 weeks
Title
Patient reported indirect economical expences due to shoulder pain; production loss.
Description
Patient reported production loss measured as patient estimated per cent production loss due to shoulder pain. A higher number means a higher loss of production.
Time Frame
Measured at 0, 6, 12, 52 weeks
Title
Work disability from the Norwegian Labour and Welfare Administration registry
Description
Registry data
Time Frame
Measured at 52 weeks
Title
Global patient perceived satisfaction with treatment
Description
1 item (5-point Likert scale); 0=dissatisfied, 5=very satisfied
Time Frame
Measured at 6, 12, 52 weeks
Title
Patient experience questionnaire (PEQ)
Description
4 subscales (communication, emotions, outcome, barriers) with 4 items measured on 4 or 7 point Likert scales. A high score represents a good communication experience, positive emotions, positive consultation outcome, no communication barriers.
Time Frame
Measured at 0 weeks
Title
Patient Shoulder Outcome Expectancies
Description
1 item measured on a 7-point Likert scale. A higher score indicate higher patient perceived outcome expectancy.
Time Frame
Measured at 0 week, 12 weeks
Title
Patient interview (qualitative)
Description
Qualitative interview with selected patients, feasibility/ barriers and facilitators
Time Frame
Measured at 52 weeks
Title
Implementation process assesment tool (IPAT)
Description
Measurement of the implementation process from the perspective of the GPs
Time Frame
Measured at 2 weeks, 12 weeks
Title
GPs self-efficacy for handling patients with shoulder pain according to guideline care
Description
9 items measured on 6-point Likert scales analysing change in individual items and sum score before and 12 weeks after educational outreach. A higher score indicates higher self-efficacy
Time Frame
Measured at 0 week, 2 weeks,12 weeks
Title
GPs global perceived satisfaction with workshop (GP)
Description
10 item measured on 5-point Likert scales concerning satisfaction with the different topics and content of the work shop.We will analyze individual items. A higher score indicate higher satisfaction.
Time Frame
Measured at 0 weeks
Title
GPs global perceived satisfaction, benefit, usability and frequency of use of the intervention (GP)
Description
4 item measured on 5-point Likert scales. We will analyze individual items. A higher score indicate higher satisfaction, benefit, usability and frequency of use of the intervention.
Time Frame
Measured at 12 weeks
Title
GPs use of the intervention in daily practice; degree of simplifying shoulder evaluation and treatment, recommending exercises, information and patient involvement (GP)
Description
4 items measured on 7-point Likert scales. We will analyze individual items. A higher score indicate higher degree of use in daily practice and a higher degree of simplifying shoulder evaluation and treatment, recommending exercises, information and patient involvement.
Time Frame
Measured at 12 weeks
Title
GP focus groups
Description
Qualitative interview with selected GPs, feasibility/ barriers and facilitators
Time Frame
Measured at 52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pain in the shoulder region Above 18 years Exclusion Criteria: Unable to fill in self-report questionnaires or do not understand Norwegian Acute injury with clinical suspicion of fracture, luxation of shoulder joints or large tendon ruptures Clinical suspicion of referred pain to the shoulder area from other organs Signs of inflammatory joint disease Suspicion of malignant disease Symptoms and signs of cervical radiculopathy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stein J Pedersen, MD
Phone
90162213
Ext
+47
Email
s.j.pedersen@medisin.uio.no
First Name & Middle Initial & Last Name or Official Title & Degree
Ole M Ekeberg, MD, PhD
Phone
91745757
Ext
+47
Email
omae@helse-fonna.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Niels G Juel, MD, PhD
Organizational Affiliation
Department of General practice, University of Oslo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Research and innovation, Helse Fonna, Norway
City
Haugesund
State/Province
Vestland
ZIP/Postal Code
5504
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ole M Ekeberg, MD, PhD
Phone
91745757
Ext
+47
Email
omae@helse-fonna.no
First Name & Middle Initial & Last Name & Degree
Eva Biringer, MD, PhD
Phone
97156593
Ext
+47
Email
eva.kristin.hope.aaker.biringer@helse-fonna.no
Facility Name
Department of General Practice, University of Oslo
City
Oslo
ZIP/Postal Code
0450
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stein J Pedersen, MD
Phone
90162213
Ext
+47
Email
s.j.pedersen@medisin.uio.no
First Name & Middle Initial & Last Name & Degree
Niels G Juel, MD, PhD
Phone
92443113
Ext
+47
Email
UXNGJU@ous-hf.no

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22310560
Citation
Curran GM, Bauer M, Mittman B, Pyne JM, Stetler C. Effectiveness-implementation hybrid designs: combining elements of clinical effectiveness and implementation research to enhance public health impact. Med Care. 2012 Mar;50(3):217-26. doi: 10.1097/MLR.0b013e3182408812.
Results Reference
background
PubMed Identifier
28637737
Citation
Artus M, van der Windt DA, Afolabi EK, Buchbinder R, Chesterton LS, Hall A, Roddy E, Foster NE. Management of shoulder pain by UK general practitioners (GPs): a national survey. BMJ Open. 2017 Jun 21;7(6):e015711. doi: 10.1136/bmjopen-2016-015711.
Results Reference
background
PubMed Identifier
34996788
Citation
Ekeberg OM, Pedersen SJ, Natvig B, Brox JI, Biringer EK, Endresen Reme S, Engebretsen KB, Joranger P, Mdala I, Juel NG. Making shoulder pain simple in general practice: implementing an evidence-based guideline for shoulder pain, protocol for a hybrid design stepped-wedge cluster randomised study (EASIER study). BMJ Open. 2022 Jan 7;12(1):e051656. doi: 10.1136/bmjopen-2021-051656.
Results Reference
derived

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Simple and Evidence-based Examination and Treatment of Shoulder Pain in General Practice

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