Finding the minimal intervention needed for sustained mammography adherence.

Published

Journal Article

BACKGROUND: Regular adherence to mammography screening saves lives, yet few women receive regular mammograms. DESIGN: RCT. SETTING/PARTICIPANTS: Participants were recruited through a state employee health plan. All were women aged 40-75 years and had recent mammograms prior to enrollment (n=3547). Data were collected from 2004 to 2009. INTERVENTION: Trial tested efficacy of a two-step adaptively-designed intervention to increase mammography adherence over 4 years. The first intervention step consisted of three reminder types: enhanced usual care reminders (EUCR); enhanced letter reminders (ELR); both delivered by mail, and automated telephone reminders (ATR). After delivery of reminders, women who became off-schedule in any of the 4 years received a second step of supplemental interventions. Three supplemental intervention arms contained priming letters and telephone counseling: barriers only (BarriCall); barriers plus positive consequences of getting mammograms (BarriConCall+); and barriers plus negative consequences of not getting mammograms (BarriConCall-). MAIN OUTCOME MEASURES: Average cumulative number of days non-adherent to mammography over 4 years based on annual screening guidelines (analyses conducted in 2009). RESULTS: All reminders performed equally well in reducing number of days of non-adherence. Women randomized to receive supplemental interventions had significantly fewer days of non-adherence compared to women who received EUCR (p=0.0003). BarrConCall+ and BarrConCall- conditions did not significantly differ in days non-adherent compared to women in the barriers-only condition (BarriCon). CONCLUSIONS: The minimal intervention needed for sustained mammography use is a combination of a reminder followed by a priming letter and barrier-specific telephone counseling for women who become off-schedule. Additional costs associated with supplemental interventions should be considered by organizations deciding which interventions to use. TRIAL REGISTRATION NUMBER: NCT01148875.

Full Text

Duke Authors

Cited Authors

  • Gierisch, JM; DeFrank, JT; Bowling, JM; Rimer, BK; Matuszewski, JM; Farrell, D; Skinner, CS

Published Date

  • October 2010

Published In

Volume / Issue

  • 39 / 4

Start / End Page

  • 334 - 344

PubMed ID

  • 20837284

Pubmed Central ID

  • 20837284

Electronic International Standard Serial Number (EISSN)

  • 1873-2607

Digital Object Identifier (DOI)

  • 10.1016/j.amepre.2010.05.020

Language

  • eng

Conference Location

  • Netherlands