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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03665870
Other study ID # UAB-CHSP-2017-1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2018
Est. completion date July 20, 2020

Study information

Verified date July 2020
Source University of Alabama at Birmingham
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to standardize and evaluate the benefits of the Prevention to Intervention program offered by the Birmingham Fire and Rescue Service. This will accomplished by standardizing the educational materials used, offering phone based follow-up and pre-post data collection.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date July 20, 2020
Est. primary completion date May 24, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 64 Years
Eligibility Inclusion Criteria:

1. Be a citizen of Birmingham

2. Be 18 years or older

3. Receive Dextrose-50 IV (intravenous treatment provided by EMS personnel for hypoglycemia)

4. Understand and speak English

Exclusion Criteria:

a) Enrolled currently in any diabetes related educational programs

Study Design


Intervention

Behavioral:
Hypoglycemia Education
Two in-person visits to the home of the participant and 4 phone calls will be conducted to provided education on prevention of hypoglycemia.

Locations

Country Name City State
United States Birmingham Fire and Rescue Service Birmingham Alabama

Sponsors (2)

Lead Sponsor Collaborator
University of Alabama at Birmingham Birmingham Fire and Rescue Service

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fear of Hypoglycemia One of the most important impact of hypoglycemia, is non-compliance to diabetes treatment due to the fear of hypoglycemia. This would be measured using the "Hypoglycemia Scale: FH-15" scale. Through study completion, an average of 8 weeks
Secondary Self Efficacy Measured using the "Perceived Diabetes Self-Management Scale". Pre and Post (after 8 weeks)Through study completion, an average of 8 weeks
Secondary Knowledge of Diabetes Measured using the "The Knowledge in Low Literacy in Diabetes Knowledge Assessment Scale" Through study completion, an average of 8 weeks
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