Strategies to Increase Cervical Cancer Screening With Mailed Human Papillomavirus Self-Sampling Kits: A Randomized Clinical Trial.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
28 11 2023
Historique:
pmc-release: 28 05 2024
medline: 29 11 2023
pubmed: 28 11 2023
entrez: 28 11 2023
Statut: ppublish

Résumé

Optimal strategies for increasing cervical cancer screening may differ by patient screening history and health care setting. Mailing human papillomavirus (HPV) self-sampling kits to individuals who are overdue for screening increases adherence; however, offering self-sampling kits to screening-adherent individuals has not been evaluated in the US. To evaluate the effectiveness of direct-mail and opt-in approaches for offering HPV self-sampling kits to individuals by cervical cancer screening history (screening-adherent and currently due, overdue, or unknown). Randomized clinical trial conducted in Kaiser Permanente Washington, a US integrated health care delivery system. Individuals aged 30 to 64 years with female sex, a primary care clinician, and no hysterectomy were identified through electronic health records (EHRs) and enrolled between November 20, 2020, and January 28, 2022, with follow-up through July 29, 2022. Individuals stratified as due (eg, at the time of randomization, these individuals have been previously screened and are due for their next screening in ≤3 months) were randomized to receive usual care (patient reminders and clinician EHR alerts [n = 3671]), education (usual care plus educational materials about screening [n = 3960]), direct mail (usual care plus educational materials and a mailed self-sampling kit [n = 1482]), or to opt in (usual care plus educational materials and the option to request a kit [n = 3956]). Individuals who were overdue for screening were randomized to receive usual care (n = 5488), education (n = 1408), or direct mail (n = 1415). Individuals with unknown history for screening were randomized to receive usual care (n = 2983), education (n = 3486), or to opt in (n = 3506). The primary outcome was screening completion within 6 months. Primary analyses compared direct-mail or opt-in participants with individuals randomized to the education group. The intention-to-treat analyses included 31 355 randomized individuals (mean [SD] age, 45.9 [10.4] years). Among those who were due for screening, compared with receiving education alone (1885 [47.6%]), screening completion was 14.1% (95% CI, 11.2%-16.9%) higher in the direct-mail group (914 [61.7%]) and 3.5% (95% CI, 1.2%-5.7%) higher in the opt-in group (2020 [51.1%]). Among individuals who were overdue, screening completion was 16.9% (95% CI, 13.8%-20.0%) higher in the direct-mail group (505 [35.7%]) compared with education alone (264 [18.8%]). Among those with unknown history, screening was 2.2% (95% CI, 0.5%-3.9%) higher in the opt-in group (634 [18.1%]) compared with education alone (555 [15.9%]). Within a US health care system, direct-mail self-sampling increased cervical cancer screening by more than 14% in individuals who were due or overdue for cervical cancer screening. The opt-in approach minimally increased screening. To increase screening adherence, systems implementing HPV self-sampling should prioritize direct-mail outreach for individuals who are due or overdue for screening. For individuals with unknown screening history, testing alternative outreach approaches and additional efforts to document screening history are warranted. ClinicalTrials.gov Identifier: NCT04679675.

Identifiants

pubmed: 38015219
pii: 2812323
doi: 10.1001/jama.2023.21471
pmc: PMC10685881
doi:

Banques de données

ClinicalTrials.gov
['NCT04679675']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1971-1981

Subventions

Organisme : NCI NIH HHS
ID : R01 CA240375
Pays : United States

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Auteurs

Rachel L Winer (RL)

Department of Epidemiology, University of Washington, Seattle.
Kaiser Permanente Washington Health Research Institute, Seattle.

John Lin (J)

Department of Epidemiology, University of Washington, Seattle.

Melissa L Anderson (ML)

Kaiser Permanente Washington Health Research Institute, Seattle.

Jasmin A Tiro (JA)

Biological Sciences Division, Department of Public Health Sciences, University of Chicago, Chicago, Illinois.

Beverly B Green (BB)

Kaiser Permanente Washington Health Research Institute, Seattle.
Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, California.

Hongyuan Gao (H)

Kaiser Permanente Washington Health Research Institute, Seattle.

Richard T Meenan (RT)

Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon.

Kristina Hansen (K)

Kaiser Permanente Washington Health Research Institute, Seattle.

Angela Sparks (A)

Washington Permanente Medical Group, Seattle.
UnitedHealthcare Community Plan of Washington, SeaTac.

Diana S M Buist (DSM)

Department of Epidemiology, University of Washington, Seattle.
GRAIL LLC, Menlo Park, California.

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