Barely Significant
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Health system interventions to integrate genetic testing in routine oncology services: A systematic review.

PLoS One · 2021 · PMC8133413 · PMID 34010335

1
hedged sentence
0.0200
closest p · 0.4× alpha
0.0200
boldest claim

The sentences

showed a trendp = 0.02actually significant
Another study [ 37 ] used a complex intervention consisting of health professional and patient education (written information, family history collection proforma), documentation (EMR documentation of referral for GC/GT and testing protocol pathway) and systems (scheduling GC appointments directly at gynaecology clinic) showed a trend towards the intervention for GC referral (+27.4 (95% CI 11.1–43.7) p = 0.02) and completion of GT (+20.6 (95% CI 5.9–35.4) and towards the control for completion of GC (-27.8 (95% CI -46.7 to -9.1)) and identifying hereditary cancer (- 17.9 (95% CI– 40.9–5.1) p = 0.17).

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