Minnesota Coron women1989.
Methods | ||
Participants | Institutionalised women living in a mental hospital (USA) CVD risk: low Control: randomised 2320, analysed unclear Intervention: randomised 2344, analysed unclear Mean years in trial: control 1.0, intervention 1.1 % male: 0 Age: unclear, ranges from <30 to >70 | |
Interventions | Modified fat diet vs. usual diet Control aims: usual institutional diet provided Intervention aims: institutional diet modified to total fat 45%E, PUFA 18‐20%E, P/S 2.5, less than 150mg/day dietary chol Control methods: whole diet provided Intervention methods: whole diet provided Total fat intake (over 4 years): mod fat 37.8 (sd unclear)%E, cont 39.1 (sd unclear)%E Saturated fat intake (over 4 years): mod fat 9.2 (sd unclear)%E, cont 18.3 (sd unclear)%E Style: diet provided Setting: residential institution |
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Outcomes | Stated trial outcomes: MI, mortality, sudden deaths
Data available on total mortality? yes
Cardiovascular mortality? yes
Events available for combined cardiovascular events: total MI plus sudden death plus stroke Secondary outcomes: stroke, cancer deaths, total MI Tertiary outcomes: none (data provided on total cholesterol and TGs but no variance info) |
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Notes | This was a 4.5 year institutional study, but as turnover of participants was very high average time in trial per participant was actually around one year. Participants were replaced as they left, and often left the institution and later returned. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | "stratified randomisation" |
Allocation concealment (selection bias) | Unclear risk | Randomisation method not clearly described |
Blinding (performance bias and detection bias) All outcomes | Low risk | Physician blinding: adequate Participant blinding: adequate |
Incomplete outcome data (attrition bias) All outcomes | High risk | No, participants appear to have been lost on leaving the institution |
Selective reporting (reporting bias) | Low risk | Not relevant for primary and secondary outcomes as all trialists asked for data |
Other bias | Low risk | |
Free of systematic difference in care? | Low risk | Whole diet provided for both groups. See Control and Intervention Methods in Interventions section of the Table of Characteristics of Included Studies |
Free of dietary differences other than fat? | Low risk | See Control and Intervention Aims in Interventions section of the Table of Characteristics of Included Studies |