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Completed

NCT Number: NCT07163923

MIND Diet in Relation to Malnutrition and Depression in AD

The aim of this study was to examine the association between depression, malnutrition, and the Mediterranean-Dietary Approaches to Stop Hypertension Diet Intervention for Neurodegenerative Delay (MIND) diet in Alzheimer's disease patients. This study included 30 patients with Alzheimer's disease (AD) and 30 healthy controls. A questionnaire form including sociodemographic characteristics was applied to the individuals. In addition, anthropometric measurements, biochemical parameters, nutritional status (Food Frequency Questionnaire (FFQ), Mini Nutritional Assessment-Short Form (MNA-SF), Geriatric Nutritional Risk Index (GNRI) and MIND diet scores) and mental health status (Beck Depression Inventory (BDI), Beck Anxiety Inventory (BAI)).

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Key information

About this study

Significant progress has been made in understanding the neurobiological basis and treatment approaches for Alzheimer's disease (AD) and depression; however, the biological link between these two disorders has not yet been fully elucidated. A deeper understanding of this relationship could contribute to the development of more effective strategies for the prevention and treatment of both conditions. In this context, lifestyle-based interventions, such as nutrition, which have been shown to support cognitive health, emerge as a potential preventive and therapeutic approach. Therefore, the aim of this study was to examine the relationship between depression, malnutrition, and the Mediterranean-Dietary Approaches to Stop Hypertension Diet Intervention for Neurodegenerative Delay (MIND) diet in individuals with AD.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged over 60 years.
  • Diagnosed with Alzheimer's disease (AD) (for AD group)
  • Able to communicate with themselves or their companions
  • Healthy volunteers without systemic or neurological diseases (for control group)
  • Matching criteria: Age, gender, smoking status, and alcohol use

Exclusion criteria

  • Chronic inflammatory diseases
  • Schizophrenia
  • Bipolar disorder
  • Amputations
  • Neoplastic disorders
  • End-stage liver disease
  • End-stage kidney disease

Treatment and study plan

Primary outcomes

  1. Questionnaire Form

    Time frame: 4 months

    Sociodemographic characteristics of the individuals (age, gender, smoking and alcohol use, constipation status, swallowing-chewing problem) were questioned.

  2. Body weight (BW)

    Time frame: 4 months

    BW was measured using a calibrated digital scale placed on a flat, tiled surface. The scale was sensitive to 100 grams.

  3. Height

    Time frame: 4 months

    Height was measured using a stadiometer with the participant's head positioned in the Frankfort plane and feet placed together.

  4. Waist Circumference (WC)

    Time frame: 4 months

    WC was measured at the midpoint between the lowest rib and the iliac crest (cristal point) using a flexible measuring tape.

  5. Hip Circumference (HC)

    Time frame: 4 months

    HC was measured at the widest point of the hips using a flexible measuring tape.

  6. Body Mass Index (BMI)

    Time frame: 4 months

    BMI was calculated by dividing body weight (in kilograms) by the square of height (in meters): BMI = weight (kg) / height² (m²).

  7. Fasting Blood Glucose

    Time frame: 4 months

    Fasting blood glucose was measured using standard laboratory techniques during routine outpatient visits.

  8. Triglycerides

    Time frame: 4 months

    Triglyceride levels were measured via fasting blood samples analyzed in the outpatient clinic laboratory.

  9. LDL-Cholesterol

    Time frame: 4 months

    LDL-cholesterol was measured from fasting serum samples using standard enzymatic colorimetric methods.

  10. Total Cholesterol

    Time frame: 4 months

    Total cholesterol was measured using routine biochemical analysis in a certified laboratory.

  11. Albumin

    Time frame: 4 months

    Serum albumin levels were measured using routine laboratory procedures in outpatient visits.

  12. Vitamin D

    Time frame: 4 months

    Serum vitamin D (25(OH)D) levels were assessed using chemiluminescence immunoassay methods in the outpatient clinic laboratory.

  13. Folic Acid

    Time frame: 4 months

    Serum folic acid levels were measured using standard automated immunoassay techniques.immunoassay methods in the outpatient clinic laboratory.

  14. Vitamin B12

    Time frame: 4 months

    Serum vitamin B12 concentrations were measured using automated chemiluminescent immunoassay.immunoassay methods in the outpatient clinic laboratory.

  15. Food Frequency Questionnaire

    Time frame: 4 months

    The foods consumed by individuals in the last month were evaluated across seven different groups, including five basic food groups (meat and meat products, milk and dairy products, bread and grains, vegetables and fruits, sugar and fats), beverages, and fast food. Participants were asked how often they consumed foods and beverages in these groups; responses were collected using the following options: "every meal," "every day," "5-6 days a week," "3-4 days a week," "1-2 days a week," "once every 15 days," "once a month," and "never." To determine the average daily consumption amounts based on consumption frequency, the following coefficients were used: 3 for "every meal," 1 for "every day," 0.7855 for "5-6 times a week," 0.498 for "3-4 times a week," 0.2145 for "1-2 times a week," 0.067 for "every 15 days," and 0.033 for "once a month."

  16. MIND diet compliance score

    Time frame: 4 months

    It includes a total of 15 different food groups, ten groups that protect brain health and five groups that harm brain health. By examining the Food Frequency Questionnaire of individuals, the amount of consumption of foods belonging to these 15 groups was divided into portions and evaluated in accordance with the scoring. It is scored between 0-15 and there is no cut-off point for determining compliance with the Mediterranean-Dietary Approaches to Stop Hypertension Diet Intervention for Neurodegenerative Delay (MIND) diet. It has been reported that the higher the score, the higher the compliance with the MIND diet. The Food Frequency Questionnaire of the items reflecting each MIND diet component were quantified in terms of how many days per week individuals consumed the food item.

  17. Geriatric Nutritional Risk Index (GNRI)

    Time frame: 4 months

    It was first introduced to evaluate the nutritional status of elderly, bedridden care patients. GNRI is calculated using height, weight and serum albumin values of the patients. GNRI [1.489 x albumin (g/l)] + [ 41.7 x (body weight / ideal body weight)]. According to the GNRI results, they are divided into four groups. Malnutrition grades are grouped as GNRI<82; severe malnutrition, moderate malnutrition between 82-92, mild malnutrition between 92-98, and no risk for malnutrition above 98.

  18. Mini Nutritional Assessment-Short Form (MNA-SF)

    Time frame: 4 months

    It is a screening tool used to evaluate malnutrition in elderly individuals. The tool includes six items that assess various factors such as appetite changes, unintentional weight loss over the past three months, neuropsychological issues, presence of psychological stress or acute illness, mobility, and BMI. Based on the total score, individuals are categorized into three nutritional status groups: 0-7 points: Malnourished (indicating nutritional deficiency), 8-11 points: At risk of malnutrition, 12-14 points: Normal nutritional status.

  19. Beck Depression Inventory (BDI)

    Time frame: 4 months

    The BDI was developed to measure behavioral symptoms of depression in adolescents and adults. The inventory was revised to remove repetitive statements describing severity levels and to ask individuals to assess not only their mood on that day but also their mood over the past week. The scores obtained from the inventory are classified as follows to determine the severity of depression: 0-9 points: Minimal depression, 10-16 points: Mild depression, 17-29 points: Moderate depression, 30-63 points: Severe depression.

  20. Beck Anxiety Inventory (BAI)

    Time frame: 4 months

    It was originally developed to assess the intensity and frequency of anxiety symptoms reported by individuals. This self-assessment tool comprises 21 items, each rated on a scale from 0 (not at all) to 3 (severely). The total possible score ranges between 0 and 63, and the anxiety level is interpreted based on the total score as follows: 0-7: Minimal anxiety, 8-15: Mild anxiety, 16-22: Moderate anxiety, 23-63: Severe anxiety.

Sponsors and collaborators

Lead sponsor

Abant Izzet Baysal University

Other

Registry information

Official study title

The Role of the MIND Diet in Alzheimer's Disease Patients: A Case-Control Study on Malnutrition and Depression

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Sep 9, 2025
Registry last updated
Sep 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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