RecruitingNot ApplicableNCT05745194

Influence of Nutrition in Depression Treatment (INDEPT)

Nutritional Counselling Promoting Adherence to the Mediterranean Diet as Adjuvant in the Treatment of Major Depressive Disorder: A Randomized Open Controlled Trial Study


Sponsor

Associacao para Investigacao e Desenvolvimento da Faculdade de Medicina - CETERA

Enrollment

190 participants

Start Date

Jun 5, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The hypothesis to be tested by this study is that an intervention promoting adherence to the MedDiet can decrease symptoms of depression in patients with elevated inflammation biomarkers, namely C-reactive protein (CRP) and Interleukin 6 (IL-6) diagnosed with Major Depression Disorder (MDD), under treatment with antidepressant medication for a period of time less than or equal to 6 months. The main aim of this study is to understand if promoting the adherence to the MedDiet, as an adjuvant strategy in the treatment of MDD, is effective in decreasing symptoms of depression in MDD patients, with elevated levels of inflammation biomarkers. Other specific objectives of the study are 1. To assess the association between adherence to MedDiet and changes in inflammatory biomarkers; 2. To assess the association between changes in inflammatory biomarkers with symptoms of MDD; 3. To evaluate the association between adherence to MedDiet and effectiveness of psychiatric treatment of MDD; 4. To characterize the association between adherence to MedDiet and changes in health-related quality of life 5. To evaluate the economic cost-effectiveness of dietary counselling, as an adjuvant treatment in MDD. The study will have a duration of 12 weeks, with a randomized parallel-group open controlled trial design, with two parallel groups with an allocation ratio of 1:1 - (a) intervention arm with six nutritional consultations with a registered nutritionist, promoting adherence to MedDiet, in addition to MDD Treatment-As-Usual (TAU) and (b) control group arm benefitting only from MDD TAU. A follow up assessment will be performed at 6- and 12-months. Having into consideration an attrition of 40 percentage at the end of the intervention, the minimum sample size estimated is 190 (95 per arm). The main outcome of the trial, changes in symptoms of depression, will be evaluated using the Beck Depression Inventory Second Edition (BDI-II).


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is exploring whether following a Mediterranean diet can improve outcomes for people being treated for depression who also show signs of inflammation in their blood. Researchers suspect that food choices may play an important role alongside antidepressant medication. **You may be eligible if...** - You are 18–70 years old - You have a diagnosis of major depressive disorder (MDD) - You are currently taking an antidepressant (SSRI or SNRI) at a stable dose for at least 6 weeks - Your depression symptoms are at least mild (based on a questionnaire) - You have elevated inflammation markers in your blood (CRP or IL-6) - You are able to follow a Mediterranean diet without significant allergies or restrictions **You may NOT be eligible if...** - You have an autoimmune disease, thyroid disorder, or cancer - You have bipolar disorder, psychosis, or an eating disorder - You have had an infection in the 2 weeks before your blood test - You are pregnant or breastfeeding - You are taking glucocorticoids or NMDA receptor antagonist medications - You are currently in another study targeting diet, exercise, or depression treatment Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALPromotion of adherence to the MedDiet

Participants will be followed in six individual nutrition consultations with a duration of 30 to 60 minutes. The consultations will be focused on promoting the adherence to the MedDiet. The nutritional intervention will be personalized to each individual ad libitum, without calories or macronutrients restriction and without the goal to promote weight change. The intervention will begin with an initial assessment of the dietary patterns of the participants in which the nutritionist will identify potential behavioural changes to promote adjustments in dietary habits and therefore adherence to the MedDiet. The intervention will promote positive recommendations (behaviours recommended to follow) and negative recommendations (behaviours recommended to reduce or eliminate) (26), using the strategy and MedDiet definition proposed by Estruch et al. in the "Primary Prevention of Cardiovascular Disease with a Mediterranean Diet" study (3). The participants will also maintain MDD TAU.


Locations(2)

Hospital de Beatriz Ângelo - Hospital de Loures, EPE

Loures, Lisbon District, Portugal

Centro Hospitalar de Leiria - Hospital Santo André

Leiria, Portugal

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NCT05745194


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