Here is the structured PICO analysis for the fifty-second article you uploaded:
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Full Title (verbatim and exact):
“Effects of two feedback interventions on end-of-life outcomes in nursing home residents with dementia: A cluster-randomized controlled three-armed trial”
Boogaard JA, de Vet HCW, van Soest-Poortvliet MC, Anema JR, Achterberg WP, van der Steen JT
Palliative Medicine (2018); 32(3):693–702
DOI: https://doi.org/10.1177/0269216317750071
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Type of Article:
Cluster-randomised controlled trial (three-arm)
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PICO Analysis:
Population:
- Bereaved family caregivers of nursing home residents with dementia
- 18 Dutch nursing homes with psychogeriatric units (1790 beds)
- Inclusion: residents with dementia who stayed ≥16 days in the last month of life, and a family caregiver who could complete post-mortem questionnaires in Dutch
Intervention:
Two types of feedback interventions based on the End-of-Life in Dementia (EOLD) instruments:
- Generic feedback: aggregated, anonymous family feedback scores benchmarked against a national norm
- Feedback reports included statistically flagged strengths/deficits and improvement suggestions
- Patient-specific feedback: individual family caregiver feedback reports discussed in team meetings
- Accompanied by practical suggestions but no benchmarking
Both strategies encouraged multidisciplinary teams to discuss results and implement improvement actions
Comparator:
- No feedback (control group): nursing homes received feedback only after the study ended
Outcome:
1. Person-centred outcomes:
- Perceived quality of care (EOLD–Satisfaction With Care, range 10–40)
- Comfort in dying (EOLD–Comfort Assessment in Dying, range 14–42)
- Subscales: physical distress, dying symptoms, emotional distress, well-being
2. Process outcomes:
- Generic feedback group:
- 5 of 6 homes discussed results; only 4 implemented any actions
- Most feedback was positive (flagged green), leading to little incentive for improvement
- Associated with a statistically significant decline in perceived quality of care (–2.41 adjusted; 95% CI: –4.07 to –0.76)
- Patient-specific feedback group:
- Implemented more improvement actions (n=33) than generic group (n=10)
- Showed a non-significant trend toward better comfort (EOLD-CAD: +1.88; 95% CI: –0.34 to 4.10)
- Significant improvement in the Dying Symptoms subscale (+1.18 adjusted; 95% CI: 0.38 to 2.00)
3. Health system outcomes:
- Neither intervention significantly changed the overall comfort or burden of dying
- Implementation was limited due to:
- High baseline satisfaction scores (little room to improve)
- Minimal documentation of follow-through actions
- Limited staff involvement beyond physicians
- The authors caution that positive feedback might reduce improvement motivation, and that multidisciplinary engagement and repeated feedback cycles are likely necessary
Summary Conclusion:
This trial found that generic feedback may paradoxically lower perceived care quality, potentially due to reassurance from already favourable scores. Patient-specific feedback showed modest improvement in symptom comfort, particularly in the final days of life, but overall effects were small. Active team participation, structured goal setting, and regular follow-up may be required to translate feedback into meaningful improvements. These findings are relevant for palliative quality improvement initiatives using family-based feedback in residential aged care.
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