Prevention of depression through nutritional strategies in high-risk persons: rationale and design of the MooDFOOD prevention trial

Obesity and depression are two prevalent conditions that are costly to individuals and society. The bidirectional association of obesity with depression, in which unhealthy dietary patterns may play an important role, has been well established. Few experimental studies have been conducted to investi...

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Veröffentlicht in:BMC psychiatry 2016-06, Vol.16 (1), p.192-192, Article 192
Hauptverfasser: Roca, Miquel, Kohls, Elisabeth, Gili, Margalida, Watkins, Ed, Owens, Matthew, Hegerl, Ulrich, van Grootheest, Gerard, Bot, Mariska, Cabout, Mieke, Brouwer, Ingeborg A, Visser, Marjolein, Penninx, Brenda W
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container_issue 1
container_start_page 192
container_title BMC psychiatry
container_volume 16
creator Roca, Miquel
Kohls, Elisabeth
Gili, Margalida
Watkins, Ed
Owens, Matthew
Hegerl, Ulrich
van Grootheest, Gerard
Bot, Mariska
Cabout, Mieke
Brouwer, Ingeborg A
Visser, Marjolein
Penninx, Brenda W
description Obesity and depression are two prevalent conditions that are costly to individuals and society. The bidirectional association of obesity with depression, in which unhealthy dietary patterns may play an important role, has been well established. Few experimental studies have been conducted to investigate whether supplementing specific nutrients or improving diet and food-related behaviors can prevent depression in overweight persons. The MooDFOOD prevention trial examines the feasibility and effectiveness of two different nutritional strategies [multi-nutrient supplementation and food-related behavioral change therapy (FBC)] to prevent depression in individuals who are overweight and have elevated depressive symptoms but who are not currently or in the last 6 months meeting criteria for an episode of major depressive disorder (MDD). The randomized controlled prevention trial has a two-by-two factorial design: participants are randomized to daily multi-nutrient supplement (omega-3 fatty acids, calcium, selenium, B-11 vitamin and D-3 vitamin) versus placebo, and/or FBC therapy sessions versus usual care. Interventions last 12 months. In total 1000 participants aged 18-75 years with body mass index between 25-40 kg/m(2) and with a Patient Health Questionnaire-9 score ≥ 5 will be recruited at four study sites in four European countries. Baseline and follow-up assessments take place at 0, 3, 6, and 12 months. Primary endpoint is the onset of an episode of MDD, assessed according to DSM-IV based criteria using the MINI 5.0 interview. Depressive symptoms, anxiety, food and eating behavior, physical activity and health related quality of life are secondary outcomes. During the intervention, compliance, adverse events and potentially mediating variables are carefully monitored. The trial aims to provide a better understanding of the causal role of specific nutrients, overall diet, and food-related behavior change with respect to the incidence of MDD episodes. This knowledge will be used to develop and disseminate innovative evidence-based, feasible, and effective nutritional public health strategies for the prevention of clinical depression. ClinicalTrials.gov. Number of identification: NCT02529423 . August 2015.
doi_str_mv 10.1186/s12888-016-0900-z
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The bidirectional association of obesity with depression, in which unhealthy dietary patterns may play an important role, has been well established. Few experimental studies have been conducted to investigate whether supplementing specific nutrients or improving diet and food-related behaviors can prevent depression in overweight persons. The MooDFOOD prevention trial examines the feasibility and effectiveness of two different nutritional strategies [multi-nutrient supplementation and food-related behavioral change therapy (FBC)] to prevent depression in individuals who are overweight and have elevated depressive symptoms but who are not currently or in the last 6 months meeting criteria for an episode of major depressive disorder (MDD). The randomized controlled prevention trial has a two-by-two factorial design: participants are randomized to daily multi-nutrient supplement (omega-3 fatty acids, calcium, selenium, B-11 vitamin and D-3 vitamin) versus placebo, and/or FBC therapy sessions versus usual care. Interventions last 12 months. In total 1000 participants aged 18-75 years with body mass index between 25-40 kg/m(2) and with a Patient Health Questionnaire-9 score ≥ 5 will be recruited at four study sites in four European countries. Baseline and follow-up assessments take place at 0, 3, 6, and 12 months. Primary endpoint is the onset of an episode of MDD, assessed according to DSM-IV based criteria using the MINI 5.0 interview. Depressive symptoms, anxiety, food and eating behavior, physical activity and health related quality of life are secondary outcomes. During the intervention, compliance, adverse events and potentially mediating variables are carefully monitored. 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The randomized controlled prevention trial has a two-by-two factorial design: participants are randomized to daily multi-nutrient supplement (omega-3 fatty acids, calcium, selenium, B-11 vitamin and D-3 vitamin) versus placebo, and/or FBC therapy sessions versus usual care. Interventions last 12 months. In total 1000 participants aged 18-75 years with body mass index between 25-40 kg/m(2) and with a Patient Health Questionnaire-9 score ≥ 5 will be recruited at four study sites in four European countries. Baseline and follow-up assessments take place at 0, 3, 6, and 12 months. Primary endpoint is the onset of an episode of MDD, assessed according to DSM-IV based criteria using the MINI 5.0 interview. Depressive symptoms, anxiety, food and eating behavior, physical activity and health related quality of life are secondary outcomes. During the intervention, compliance, adverse events and potentially mediating variables are carefully monitored. 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The trial aims to provide a better understanding of the causal role of specific nutrients, overall diet, and food-related behavior change with respect to the incidence of MDD episodes. This knowledge will be used to develop and disseminate innovative evidence-based, feasible, and effective nutritional public health strategies for the prevention of clinical depression. ClinicalTrials.gov. Number of identification: NCT02529423 . August 2015.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27277946</pmid><doi>10.1186/s12888-016-0900-z</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Aged
Anxiety
Behavior Therapy - methods
Clinical Protocols
Complications and side effects
Depression - prevention & control
Depression, Mental
Depressive Disorder, Major - prevention & control
Diet
Diet - methods
Diet - psychology
Diet therapy
Diet Therapy - methods
Diet Therapy - psychology
Dietary Supplements
Eating behavior
Europe
Fatty acids
Feasibility Studies
Feeding Behavior - psychology
Female
Food
Food and nutrition
Food habits
Health aspects
Health care
Humans
Intervention
Male
Mental depression
Middle Aged
Nutrition research
Obesity
Obesity - diet therapy
Obesity - psychology
Overweight
Overweight - diet therapy
Overweight - psychology
Overweight persons
Prevention
Psychiatry
Psychological aspects
Quality of Life
Research Design
Risk Factors
Selenium
Study Protocol
Vitamins
Young Adult
title Prevention of depression through nutritional strategies in high-risk persons: rationale and design of the MooDFOOD prevention trial
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