Implementation Fidelity of a Virtual Adaptation of the Guiding Good Choices Program
- PMID: 40444872
- PMCID: PMC12173218
- DOI: 10.1002/jcop.70020
Implementation Fidelity of a Virtual Adaptation of the Guiding Good Choices Program
Abstract
Offering evidence-based parenting interventions to caregivers virtually has the potential to increase the reach and public health impact of interventions. As virtual adaptations to evidence-based interventions increase, attention must be paid to implementation fidelity, as high fidelity is associated with better program outcomes. This study examined implementation fidelity of a virtual adaptation of the family-based Guiding Good Choices program delivered to 292 families in primary care in three large healthcare systems during the COVID-19 pandemic. Attendance, dosage, adherence, quality of delivery, and participant engagement were examined quantitatively and qualitatively using interventionist and observer surveys, attendance records, and focus groups with interventionists. Interventionists and observers reported high levels of dosage, adherence, quality of delivery, and participant engagement, but attendance was lower than anticipated. Results suggest that delivering parenting programs virtually in primary care with high fidelity is feasible, but retaining participants may remain challenging in this modality, particularly during a global pandemic.
Keywords: Guiding Good Choices; implementation fidelity; internet adaptation; parenting program; prevention; virtual delivery.
© 2025 Wiley Periodicals LLC.
Conflict of interest statement
Conflict of Interest
Kevin Haggerty has had a long academic relationship with Guiding Good Choices (GGC) and continues to be interested in the implementation of GGC on a broad scale. Margaret Kuklinski has been studying the implementation and effectiveness of GGC for a long time and continues to be interested in its broad implementation. Nicole Eisenberg and Dalene Beaulieu have studied GGC implementation, are GGC trainers, and are interested in the program’s continued implementation. The other authors declare that they have no conflicts of interest.
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References
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Grants and funding
- U24 AT009676/AT/NCCIH NIH HHS/United States
- UH3 AT009838/AT/NCCIH NIH HHS/United States
- This work was supported within the National Institutes of Health (NIH) Pragmatic Trials Collaboratory by cooperative agreement UH3 AT009838 from the National Center for Complementary and Integrative Health (NCCIH), with co-funding from the National Institute on Drug Abuse (NIDA), Office of Behavioral and Social Sciences Research (OBSSR), and Office of Disease Prevention and Health Promotion (ODPHP). This work also received logistical and technical support from the NIH Pragmatic Trials Collaboratory Coordinating Center under award number U24 AT009676 from NCCIH, the National Institute of Allergy and Infectious Diseases (NIAID), the National Cancer Institute (NCI), the National Institute on Aging (NIA), the National Heart, Lung, and Blood Institute (NHLBI), the National Institute of Nursing Research (NINR), the National Institute of Minority Health and Health Disparities (NIMHD), the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), the NIH Office of Behavioral and Social Sciences Research (OBSSR), and the NIH Office of Disease Prevention and Health Promotion (ODPHP). The content is solely the responsibility of the authors and does not necessarily represent the official views of NCCIH, NIAID, NCI, NIA, NHLBI, NINR, NIMHD, NIAMS, OBSSR, or ODPHP, or NIH.
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