Abstract 4365696: Virtual Decentralized Study of Patient Nausea Experience on Anti-Obesity Medication (COSMOS-DIGITAL)

Background: Virtual clinical trials offer a scalable approach to evaluate patient-reported outcomes in real-world settings, particularly related to duration and severity of common side effects associated with marketed therapies. Study designs leveraging decentralized, tech-enabled platforms can be used to rapidly generate insights that may inform symptom management strategies. Aim: This study evaluated the feasibility of conducting a fully virtual decentralized clinical trial (DCT) with patients taking an anti-obesity medication (AOM) recruited from a digital health online community. Methods: Adult members of a US-based online digital community who self-reported use of an AOM—tirzepatide or semaglutide—for weight management were eligible for the study if willing to complete an at-home blood draw and surveys that were delivered and completed electronically. Study activities included a day 1 survey, a 30-day nausea diary, an at-home microneedle blood collection and send-out lab test, a day 30 survey, and a blood draw device satisfaction survey. Surveys captured past medical history, symptom severity, mitigation strategies, and quality of life. Blood test analytes included A1c, total cholesterol, HDL-C, triglycerides, LDL-C, creatinine, and hsCRP. Results: From 276,391 emails, 480 people completed the screener within 8 business days, and the first 200 were consented and enrolled. Participants were mostly female (86%), White (88%), and employed full time (54.5%). The mean age was 54 (range, 28-78) years, and the mean BMI was 33.9 kg/m 2 . The duration of AOM varied (< 1 month, 10.0%; 1–3 months, 26.0%; 3–6 months, 23.0%; > 6 months, 41.0%; Table 1). Most participants completed the survey elements (75.5%) and blood draws (76.0%), with 93% of samples sufficient for full or partial analyte panel testing. People were satisfied with the at-home microneedle blood collection and preferred it over clinic-based blood draws. Conclusion: This study highlights the potential of virtual DCTs to support rapid recruitment and effective remote data capture in weight management research. Further work is needed to ensure the representativeness of study participants recruited from fully online communities.

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Publication Details

Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4365696
Primary Topic
Mobile Health and mHealth Applications
Type
article
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article

Abstract 4365696: Virtual Decentralized Study of Patient Nausea Experience on Anti-Obesity Medication (COSMOS-DIGITAL)

Bethany Kalich, Michael J. Mina, Jeanine M. Cordova, Brian H. Chen et al.
Circulation
Mobile Health and mHealth Applications
article

Abstract 4365696: Virtual Decentralized Study of Patient Nausea Experience on Anti-Obesity Medication (COSMOS-DIGITAL)

Bethany Kalich, Michael J. Mina, Jeanine M. Cordova, Brian H. Chen, Marisa Cruz, Paul Burton, Stanley M. Shaw
article en

Abstract

Background: Virtual clinical trials offer a scalable approach to evaluate patient-reported outcomes in real-world settings, particularly related to duration and severity of common side effects associated with marketed therapies. Study designs leveraging decentralized, tech-enabled platforms can be used to rapidly generate insights that may inform symptom management strategies. Aim: This study evaluated the feasibility of conducting a fully virtual decentralized clinical trial (DCT) with patients taking an anti-obesity medication (AOM) recruited from a digital health online community. Methods: Adult members of a US-based online digital community who self-reported use of an AOM—tirzepatide or semaglutide—for weight management were eligible for the study if willing to complete an at-home blood draw and surveys that were delivered and completed electronically. Study activities included a day 1 survey, a 30-day nausea diary, an at-home microneedle blood collection and send-out lab test, a day 30 survey, and a blood draw device satisfaction survey. Surveys captured past medical history, symptom severity, mitigation strategies, and quality of life. Blood test analytes included A1c, total cholesterol, HDL-C, triglycerides, LDL-C, creatinine, and hsCRP. Results: From 276,391 emails, 480 people completed the screener within 8 business days, and the first 200 were consented and enrolled. Participants were mostly female (86%), White (88%), and employed full time (54.5%). The mean age was 54 (range, 28-78) years, and the mean BMI was 33.9 kg/m 2 . The duration of AOM varied (< 1 month, 10.0%; 1–3 months, 26.0%; 3–6 months, 23.0%; > 6 months, 41.0%; Table 1). Most participants completed the survey elements (75.5%) and blood draws (76.0%), with 93% of samples sufficient for full or partial analyte panel testing. People were satisfied with the at-home microneedle blood collection and preferred it over clinic-based blood draws. Conclusion: This study highlights the potential of virtual DCTs to support rapid recruitment and effective remote data capture in weight management research. Further work is needed to ensure the representativeness of study participants recruited from fully online communities.

CirculationVol. 152(Suppl_3)
Amgen (United States) (US), Inspire Institute (US)
Openalex Percentile: Top 51%
Mobile Health and mHealth Applications
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