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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02418637
Other study ID # 15-000647
Secondary ID
Status Completed
Phase N/A
First received April 6, 2015
Last updated November 7, 2016
Start date April 2015
Est. completion date September 2016

Study information

Verified date November 2016
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Test the feasibility of performing worksite screening of Hypertension, Diabetes and Hyperlipidemia for six months


Description:

The investigators will be visiting farmers at the worksite monthly for six month and perform cardiovascular risk factors screening: blood pressure, blood glucose, glycosylated hemoglobin and cholesterol.

At the end of this intervention, the investigators will test the feasibility of this approach among this specific population through questionnaires.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date September 2016
Est. primary completion date September 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years and older

- agricultural workers and farm owners

Exclusion Criteria:

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Other:
Worksite screening for DM, HTN and hyperlipidemia
Six monthly visits to worksite to perform screenings

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility (Likert scale) On a likert scale, the investigators will test the applicability, acceptance and convenience of this screening approach among this agricultural workers population After six months of the intervention, the outcome will be assessed on the last site visit via questionnaire No