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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03495791
Other study ID # 14090405
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 31, 2016
Est. completion date December 31, 2021

Study information

Verified date May 2022
Source Rush University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will provide an educational intervention through means of a video to educate subjects on the risk of cardiovascular health on Rheumatoid arthritis.


Description:

Subjects will be randomized into an interventional group and non-interventional group. Both groups will perform several surveys before an educational intervention may be given. Both Groups will come back 3 months post visit to complete additional surveys.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Clinical Diagnoses of Rheumatoid Arthritis of at least 3 months by a Rheumatologist Exclusion Criteria: - Inability to communicate in English.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
YouTube Video
Educational Video

Locations

Country Name City State
United States Rush University Medical Center Chicago Illinois

Sponsors (2)

Lead Sponsor Collaborator
Rush University Medical Center Pfizer

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Heart Disease Knowledge Questionnaire 30 items survey completed at baseline (pre-intervention, post intervention), and 3 month follow-up. Change in cardiovascular knowledge at 3 months and baseline (post-intervention) will be measured against baseline pre-intervention values. 3 Months
Primary Heart Disease Fact Questionnaire 13 items survey completed at baseline (pre-intervention, post intervention), and 3 month follow-up. Change in cardiovascular awareness at 3 months and baseline (post-intervention) will be measured against baseline pre-intervention values. 3 Months
Secondary Statues of Hyperlipidemia treatment Change in hyperlipidemia treatment from Screening to 1 year. 1 Year
Secondary Cholesterol Change in Cholesterol from Screening to 1 year. 1 year
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