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NCT05725746 Clinical Trial

Feasibility of Remote Data Collection With a Point of Care Device to Measure HbA1c

Postpartum Clinical Trial

Official title:
Enhancing Cardiovascular Health Equity in Mothers and Children Through Home Visiting

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05725746
Other study ID # 202212059
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 24, 2023
Est. completion date February 21, 2024

Study information
Verified date April 2024
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Conduct a pilot study to test feasibility of doing remote data collection with a point of care device that measures HbA1c.

Description:

The foundation for cardiovascular health (CVH) is laid in early life by intergenerational interactions, passed from parent to child, that have long-lasting biological and behavioral consequences. Lifestyle interventions can promote CVH among mothers and their children over time. Academic partnerships with home visiting organizations that reach families experiencing health disparities advance intergenerational CVH equity. For this pilot study we are testing the feasibility of doing remote data collection with a point of care device that measures HbA1c to use in the main study.

Recruitment information / eligibility
Status Completed
Enrollment 18
Est. completion date February 21, 2024
Est. primary completion date February 21, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - English speaking - Screened or participating in NCT04253977 - Able to give informed consent for participation Exclusion Criteria: -

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Point of care device to measure HbA1c
After consent the participant will meet with the research team virtually to obtain HbA1c. The HbA1c self check equipment will be sent to the participant. During the video call the research team will talk the participant through obtaining their HbA1c with the point of care device.

Locations
Country Name City State
United States Washington University in St. Louis Saint Louis Missouri

Sponsors (1)
Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Feasibility to obtain HbA1c through remote data collection Feasibility will be measured by how many participants are able to obtain HbA1c measure through remote data collection and participant's satisfaction with this means of data collection. Baseline
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