AI Article Synopsis

  • The study aims to investigate how including almonds in a calorie-restricted diet affects weight loss and maintenance compared to a nut-free diet rich in carbohydrates over a 9-month period.
  • It will involve 134 adults with a specific BMI range, who will be randomly assigned to either the almond-enriched diet or the nut-free control diet, and monitored for various health and behavioral factors.
  • The research will analyze the data collected using advanced statistical methods to see how the diets impact weight and overall health over time.

Article Abstract

Introduction: Epidemiological studies indicate an inverse association between nut consumption and body mass index (BMI). However, clinical trials evaluating the effects of nut consumption compared with a nut-free diet on adiposity have reported mixed findings with some studies reporting greater weight loss and others reporting no weight change. This paper describes the rationale and detailed protocol for a randomised controlled trial assessing whether the inclusion of almonds or carbohydrate-rich snacks in an otherwise nut-free energy-restricted diet will promote weight loss during 3 months of energy restriction and limit weight regain during 6 months of weight maintenance.

Methods And Analysis: One hundred and thirty-four adults aged 25-65 years with a BMI of 27.5-34.9 kg/m will be recruited and randomly allocated to either the almond-enriched diet (AED) (15% energy from almonds) or a nut-free control diet (NFD) (15% energy from carbohydrate-rich snack foods). Study snack foods will be provided. Weight loss will be achieved through a 30% energy restriction over 3 months, and weight maintenance will be encouraged for 6 months by increasing overall energy intake by ~120-180 kcal/day (~500-750kJ/day) as required. Food will be self-selected, based on recommendations from the study dietitian. Body composition, resting energy expenditure, total daily energy expenditure (via doubly labelled water), physical activity, appetite regulation, cardiometabolic health, gut microbiome, liver health, inflammatory factors, eating behaviours, mood and personality, functional mobility and pain, quality of life and sleep patterns will be measured throughout the 9-month trial. The effects of intervention on the outcome measures over time will be analysed using random effects mixed models, with treatment (AED or NFD) and time (baseline, 3 months and 9 months) being the between and within factors, respectively in the analysis.

Ethics And Dissemination: Ethics approval was obtained from the University of South Australia Human Research Ethics Committee (201436). Results from this trial will be disseminated through publication in peer-reviewed journals, national and international presentations.

Trial Registration Number: Australian New Zealand Clinical Trials Registry (ACTRN12618001861246).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371143PMC
http://dx.doi.org/10.1136/bmjopen-2019-036542DOI Listing

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