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Reducing Shoulder Complaints in Employees With High Occupational Shoulder Exposures

NCT03159910 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2020-08-07

No results posted yet for this study

Summary

Aim: To evaluate the effectiveness of Shoulder-Café (intervention) compared to Shoulder-Guidance (control intervention) with respect to shoulder exposures and shoulder complaints.

Hypothesis: The Shoulder-Café, which unifies education, diagnostic clarification, supervised and home-based shoulder exercises, and advice from a health and safety consultant on workplace interventions, will reduce shoulder exposures and shoulder complaints more effectively than an individual-oriented control intervention with home-based shoulder exercises and written general advice on workplace interventions.

Conditions

  • Shoulder Pain

Interventions

BEHAVIORAL

Shoulder-Café

Education and individual counselling, clinical examination, supervised shoulder exercise. Some participants can be offered a workplace visit.

BEHAVIORAL

Shoulder-Guidance

Home-based shoulder exercise and written counselling.

Sponsors & Collaborators

  • Regional Hospital West Jutland

    collaborator OTHER

  • Aarhus University Hospital

    collaborator OTHER

  • University of Aarhus

    collaborator OTHER

  • Central Jutland Regional Hospital

    lead OTHER

Principal Investigators

  • Jeanette Trøstrup, MsC · Elective Surgery Centre, Silkeborg Regional Hospital, Regional Hospital Central Jutland.

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-14
Primary Completion
2020-07-01
Completion
2020-07-01

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03159910 on ClinicalTrials.gov