Literature DB >> 30854886

CGM Benefits and Burdens: Two Brief Measures of Continuous Glucose Monitoring.

Laurel H Messer1, Paul F Cook2, Molly L Tanenbaum3, Sarah Hanes3, Kimberly A Driscoll1, Korey K Hood3.   

Abstract

BACKGROUND: Continuous glucose monitors (CGM) are underutilized by individuals with type 1 diabetes (T1D), particularly during the adolescent years. Little is known about perceptions of CGM benefit and burdens, and few tools exist to quantify this information.
METHODS: Two questionnaires were developed and validated-Benefit of CGM (BenCGM) and Burdens of CGM (BurCGM)-in a sample of adolescents ages 12-19 years involved in the T1D Exchange Registry. We chose to start the validation process with adolescents given their low CGM uptake and high risk for suboptimal glycemic outcomes. Exploratory and confirmatory factor analyses were conducted to confirm factor structure and select items. The resultant scales were tested for internal reliability and convergent/divergent validity with critical diabetes and quality of life outcomes: age, depression, diabetes distress, self-efficacy, technology attitudes, and diabetes technology attitudes.
RESULTS: A total of 431 adolescents with T1D completed the questionnaires (51% female, mean age 16.3 ± 2.26, 83% white non-Hispanic, 70% having used CGM). Two single factor scales emerged, and scales were reduced to 8 items each. Those who perceived higher benefit of CGM exhibited lower diabetes distress, higher self-efficacy, and more positive attitudes toward technology. Those who perceived higher burden of CGM exhibited higher diabetes distress, lower self-efficacy, and less positive technology attitudes.
CONCLUSION: The BenCGM and BurCGM questionnaires each comprise 8-items that demonstrate robust psychometric properties for use in adolescents with T1D, and can be used to develop targeted interventions to increase CGM wear to improve diabetes management.

Entities:  

Keywords:  adolescents; continuous glucose monitoring; technology; type 1 diabetes

Mesh:

Substances:

Year:  2019        PMID: 30854886      PMCID: PMC6835174          DOI: 10.1177/1932296819832909

Source DB:  PubMed          Journal:  J Diabetes Sci Technol        ISSN: 1932-2968


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