Online Education to Improve the Management of Rotator Cuff Related Shoulder Pain
Primary Purpose
Subacromial Pain Syndrome, Rotator Cuff Injuries
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Rotator Cuff Related Shoulder Pain E-Learning Program
Sponsored by
About this trial
This is an interventional other trial for Subacromial Pain Syndrome focused on measuring Online education, Shoulder pain, Physiotherapy
Eligibility Criteria
Inclusion Criteria:
- 3th or 4th grade physiotherapy students
Exclusion Criteria:
- Students who are not currently enrolled in 3th or 4th grade
Sites / Locations
- Marmara University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
E-learning Group
Wait-list Control Group
Arm Description
Participants will enroll in a 4-week e-learning program immediately after completing the pre-intervention assessment measures.
Participants will enroll in a 4-week e-learning program, 4-5 weeks after completion of the pre-intervention assessment measures.
Outcomes
Primary Outcome Measures
Rotator cuff related shoulder pain achievement test
The RCRSP achievement test is consistent with 18 question items with multiple choices. The mean difficulty and KR-20 reliability coefficient of the test were calculated 0.59 and 0.84, respectively.
Secondary Outcome Measures
Self-reported confidence in knowledge and clinical reasoning skills related to rotator cuff related shoulder pain
The 3-item Questionnaire requires participants to rate their confidence in their knowledge and clinical skills related to RCRSP, using a 5-point Likert Scale ('not at all confident', 'not very confident', 'somewhat confident', 'confident' and 'very confident').
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04952623
Brief Title
Online Education to Improve the Management of Rotator Cuff Related Shoulder Pain
Official Title
Randomized Controlled Trial of Online Education for Physiotherapy Students to Improve the Management of Rotator Cuff Related Shoulder Pain
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
November 20, 2022 (Actual)
Primary Completion Date
February 10, 2023 (Actual)
Study Completion Date
April 3, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Marmara University
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
A randomized controlled trial: Conservative treatments including physiotherapy and rehabilitation in the management of rotator cuff-related shoulder pain (RCRSP) are generally accepted as the first-line treatment approach, however, it is known that the disease-specific physiotherapy methods used by physiotherapists are highly variable. This may be caused by the insufficient knowledge of therapists about evidence-based interventions to RCRSP. The aim of this study is to develop the '' Rotator Cuff Related Shoulder Pain E-learning Program'' and evaluate its effect on students' knowledge and clinical reasoning skills related to evidence-based RCRSP interventions and their levels of confidence to have this knowledge compared with a control group.
Detailed Description
Shoulder pain is one of society's most common musculoskeletal problems, with a prevalence defined between 16-26%. Almost 70% of shoulder pain complaints are caused by pathologies associated with the rotator cuff. Conservative treatments including physiotherapy are widely accepted as a first-line treatment approach in the management of shoulder pain and on the other hand, the variety of physiotherapy practice is conspicuous. Despite the majority of physiotherapists provide treatment in line with current evidence, passive modalities are still highly preferred by some physiotherapists. The gap between research evidence and practice could be slightly due to the lack of an up-to-date undergraduate physiotherapy curriculum about the RCRSP. Therefore, the aim of this study is to develop the '' Rotator Cuff Related Shoulder Pain E-learning Program'' and evaluate its effect on students' knowledge and clinical reasoning skills related to evidence-based RCRSP interventions and their levels of confidence to have this knowledge compared with a control group. A randomized controlled trial including 146 4th grade physiotherapy students will be conducted. Students will be randomized into an e-learning group (n=73) or wait-list control group (n=73). The primary outcome will be the RCRSP achievement test, and the secondary outcome will be the self-reported confidence in knowledge and clinical reasoning skills related to RCRSP. All data will be collected through an online survey, which will be applied in two different time periods: pre-intervention and post-intervention. All groups will first answer the questionnaire at the beginning (week 0) and after the study group's e-learning activity (4-5 weeks).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subacromial Pain Syndrome, Rotator Cuff Injuries
Keywords
Online education, Shoulder pain, Physiotherapy
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
198 (Actual)
8. Arms, Groups, and Interventions
Arm Title
E-learning Group
Arm Type
Experimental
Arm Description
Participants will enroll in a 4-week e-learning program immediately after completing the pre-intervention assessment measures.
Arm Title
Wait-list Control Group
Arm Type
Active Comparator
Arm Description
Participants will enroll in a 4-week e-learning program, 4-5 weeks after completion of the pre-intervention assessment measures.
Intervention Type
Other
Intervention Name(s)
Rotator Cuff Related Shoulder Pain E-Learning Program
Intervention Description
The RCRSP e-learning program is designed according to the ADDIE Instructional Design Model in light of current literature.
Primary Outcome Measure Information:
Title
Rotator cuff related shoulder pain achievement test
Description
The RCRSP achievement test is consistent with 18 question items with multiple choices. The mean difficulty and KR-20 reliability coefficient of the test were calculated 0.59 and 0.84, respectively.
Time Frame
Change from baseline test scores at 4 weeks
Secondary Outcome Measure Information:
Title
Self-reported confidence in knowledge and clinical reasoning skills related to rotator cuff related shoulder pain
Description
The 3-item Questionnaire requires participants to rate their confidence in their knowledge and clinical skills related to RCRSP, using a 5-point Likert Scale ('not at all confident', 'not very confident', 'somewhat confident', 'confident' and 'very confident').
Time Frame
Change from baseline self-reported scores at 4 weeks
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
3th or 4th grade physiotherapy students
Exclusion Criteria:
Students who are not currently enrolled in 3th or 4th grade
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mine Gülden Polat, PhD.
Organizational Affiliation
Marmara University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Bahar Ayberk, PhD.
Organizational Affiliation
Marmara University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Marmara University
City
İstanbul
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Online Education to Improve the Management of Rotator Cuff Related Shoulder Pain
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