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Study Characteristics and the Efficacy of the Intervention

Journal: BMC Medicine

Article Title: Evaluating digital nudge interventions for the promotion of cancer screening behavior: a systematic review and meta-analysis

doi: 10.1186/s12916-025-04028-8

Figure Lengend Snippet: Study Characteristics and the Efficacy of the Intervention

Article Snippet: Greiner et al., 2014, the USA [ ] , To test an implementation intentions (I-I) intervention for improving CRC screening rates , Precaution Adoption Process Model (PAPM) , Touchscreen computers , Individual , NR , Health center staff, research assistants , IG had higher odds of completing colorectal cancer (CRC) screening at 26 weeks (IG & CG, AOR = 1.83) ( p < 0.05) , • Self-efficacy (IG & CG, AOR = 1.56) ( p < 0.05).

Techniques:

Colorectal cancer screening: study characteristics and results of colorectal cancer screening including colonoscopy and fecal occult blood test/fecal immunochemical test ( n = 10)

Journal: European Journal of Cancer Prevention

Article Title: Interactive or tailored digital interventions to increase uptake in cervical, breast, and colorectal cancer screening to reduce health inequity: a systematic review

doi: 10.1097/CEJ.0000000000000796

Figure Lengend Snippet: Colorectal cancer screening: study characteristics and results of colorectal cancer screening including colonoscopy and fecal occult blood test/fecal immunochemical test ( n = 10)

Article Snippet: Greiner et al . (2014 ), USA , 42% non-Hispanic African American, 28% non-Hispanic white, 27% Hispanic Intervention group: n = 234 Control group: n = 236 Age 45–70 , Info and education on CRC screening. Participants responded to ‘implementations intentions’ planning questions specific to CRC screening. Interactive, multimedia touchscreen computer that used either English or Spanish text with narration through headphones, as well as pictures and video targeted to the race/ ethnicity of the participant. , Self-reported CRC screening Follow-up: 26 weeks Intervention group: 54% vs control group: 42% OR = 1.83, CI = 1.23–2.73, P ≤ 0.01.

Techniques: Control, Clarification Assay, Biomarker Discovery