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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03523884
Other study ID # UWO Firefighters 2018
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 2018
Est. completion date September 2019

Study information

Verified date April 2018
Source Western University, Canada
Contact Goris Nazari, PhD(C)
Phone 519 661 2111
Email gnazari@uwo.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess if a technology-enabled Exercise program plus Education (TEEP + E) is more effective than Education program (EP) alone, in providing better outcomes (quality of life, at-work disability and productivity loss, firefighters' perception, adherence, overall improvement/deterioration) in firefighters with shoulder pain, at 3-, 6-and 12-month follow ups.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 180
Est. completion date September 2019
Est. primary completion date June 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- Active duty firefighters aged 18 to 100 years, with shoulder pain.

- Do not permanently use strong pain medications.

- Able to understand spoken and written English.

- Access to computer, internet and telecommunications application software (Skype).

Exclusion Criteria:

- Firefighters who have had shoulder related surgeries in the last 6 months.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise Program plus Education
Rotator cuff exercises outlined in the American Academy of Orthopedic Surgeons (AAOS) guidelines on management of rotator cuff problems.
Educational Program (EP).
An information sheet form AAOS, outlining the anatomy, description, causes, symptoms, examination and imaging tests performed on individuals with shoulder conditions

Locations

Country Name City State
Canada Hamilton Fire Station Hamilton Ontario

Sponsors (1)

Lead Sponsor Collaborator
Western University, Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Firefighter Work Limitation Questionnaire at-work disability and productivity loss 3-months
Primary Firefighter Work Limitation Questionnaire at-work disability and productivity loss 6-months
Primary Firefighter Work Limitation Questionnaire at-work disability and productivity loss 12-months
Primary Short- Western Ontario Rotator Cuff Index Quality of life 3-months
Primary Short- Western Ontario Rotator Cuff Index Quality of life 6-months
Primary Short- Western Ontario Rotator Cuff Index Quality of life 12-months
Secondary Single Assessment Numeric Evaluation Patient's perception of the condition 3-, 6- and 12-months
Secondary Number of days lost Work days lost due to the condition 3-, 6- and 12-months
Secondary Therapy Adherence Assessment Tool Exercise adherence 3-, 6- and 12-months
Secondary Global Rating of Change Scale To quantify a patient's improvement or deterioration over time 6- and 12-months
Secondary Adverse Effects Have you experienced any exercise-induced pain 3-, 6- and 12-months
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