NCT04952623

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
198

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 17, 2021

Completed
20 days until next milestone

First Posted

Study publicly available on registry

July 7, 2021

Completed
1.4 years until next milestone

Study Start

First participant enrolled

November 20, 2022

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 10, 2023

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 3, 2023

Completed
Last Updated

April 6, 2023

Status Verified

October 1, 2022

Enrollment Period

3 months

First QC Date

June 17, 2021

Last Update Submit

April 4, 2023

Conditions

Keywords

Online educationShoulder painPhysiotherapy

Outcome Measures

Primary Outcomes (1)

  • 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.

    Change from baseline test scores at 4 weeks

Secondary Outcomes (1)

  • Self-reported confidence in knowledge and clinical reasoning skills related to rotator cuff related shoulder pain

    Change from baseline self-reported scores at 4 weeks

Study Arms (2)

E-learning Group

EXPERIMENTAL

Participants will enroll in a 4-week e-learning program immediately after completing the pre-intervention assessment measures.

Other: Rotator Cuff Related Shoulder Pain E-Learning Program

Wait-list Control Group

ACTIVE COMPARATOR

Participants will enroll in a 4-week e-learning program, 4-5 weeks after completion of the pre-intervention assessment measures.

Other: Rotator Cuff Related Shoulder Pain E-Learning Program

Interventions

The RCRSP e-learning program is designed according to the ADDIE Instructional Design Model in light of current literature.

E-learning GroupWait-list Control Group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • th or 4th grade physiotherapy students

You may not qualify if:

  • Students who are not currently enrolled in 3th or 4th grade

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Marmara University

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Rotator Cuff InjuriesShoulder Pain

Condition Hierarchy (Ancestors)

RuptureWounds and InjuriesShoulder InjuriesTendon InjuriesArthralgiaJoint DiseasesMusculoskeletal DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Mine Gülden Polat, PhD.

    Marmara University

    STUDY CHAIR
  • Bahar Ayberk, PhD.

    Marmara University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 17, 2021

First Posted

July 7, 2021

Study Start

November 20, 2022

Primary Completion

February 10, 2023

Study Completion

April 3, 2023

Last Updated

April 6, 2023

Record last verified: 2022-10

Data Sharing

IPD Sharing
Will not share

Locations