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The MAIA trial: Protocol of a prospective randomized controlled trial to evaluate the impact of an omega-3 polyunsaturated fatty acids-enriched diet on the loss of independence in nursing home residents

Billy C, Bajeux E, Mairesse G, Charras K, Weill P, Somme D, Thibault R

Clinical nutrition ESPEN, 2026

432 participants

Abstract

BACKGROUND

Malnutrition and frailty are prevalent issues in nursing homes, leading to increased dependence and morbidity. N-3 polyunsaturated fatty acids (PUFAs), i.e. linolenic, eicosapentaenoic, and docosahexaenoic acids, have demonstrated potential benefits in mitigating inflammation, cognitive decline, and sarcopenia. However, there is limited evidence on the impact of dietary n-3 PUFAs enrichment in preventing independence loss in the older patients and particularly nursing home (NH) residents.

OBJECTIVES

The trial aims to evaluate whether an n-3 PUFAs-enriched diet to cover the recommended daily allowance needs can slow down the decline in independence among older residents in NH.

METHODS

A prospective, randomized, controlled, open-label, multicenter trial will be conducted in NH. The study population (n = 432) will be cluster-randomized into two groups: 1- an intervention group receiving an n-3 PUFAs enriched diet, and 2- a control group receiving the usual institutional diet. The primary outcome will be the change in independence, measured by the Activities of Daily Living-Long Form Score (ADL-LFS) at 24 months. Secondary outcomes will include ADL-LFS at 6, 12, and 18 months, nutritional status, body composition, muscle function, fall incidence, infection rates, cognitive function, depression scale, n-3 and n-6 PUFAs blood levels, and healthcare resource utilization. In a subgroup of patients (n = 30 per group), data on actimetry will be collected. Statistical…

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 432 participants or records.

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