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Study identifier: NCT06535139 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

ReMARK: Addressing Disparities in Rural HPV-related Cancer Prevention

Condition: Papillomavirus Vaccines  ·  Sponsor: University of Florida

PhaseNA
Planned participants4630
Who can joinAll sexes, 8 Years to 99 Years
Healthy volunteersNo

About this study

There are three main objectives of the protocol. First, we will evaluate the added clinical- and cost- effectiveness of parent-targeted motivational aids (reminder/recall and phone-based MI) alone and when combined with community-targeted healthcare access assistance beyond the effects of clinician-targeted training. Second, we will estimate the differential effectiveness of the implementation strategies by patient-level factors (age, race/ethnicity, sex, distance from home to clinic, social vulnerability). Third, we will measure moderation of implementation strategy effectiveness by clinic-level factors (HPV vaccination priority, resources, clinic visit types, scheduling practices, and implementation success). Within 11 rural North Central Florida counties, we will evaluate the layering of evidence-based implementation strategies that progressively addressing clinician, parent, and healthcare access barriers faced by rural communities on HPV vaccination rates among 9- to 12-year-olds. To best address our main question of whether layering complementary strategies continues to increase effects on HPV vaccination, we will test our hypotheses with a three-arm cluster randomized study design of nested strategies. The proposed nested study design optimizes evaluation, causal inference, and scientific rigor by putting the maximum number of clinics towards addressing the layering of strategies. Randomization will occur at the clinic level. All clinics will receive implementation st…

This description comes directly from the study's public registry record.

Talk to the study team

Stephanie Staras, PhD  ·  352-294-8299  ·  sstaras@ufl.edu

Marta Hansen, MBA  ·  352-627-9075  ·  m.hansen1@ufl.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of FloridaGainesville, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06535139