MIND Diet and Cognitive Function in Adults With MCI

Sponsor
Zhejiang University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05975723
Collaborator
(none)
240
1
2
24.2
9.9

Study Details

Study Description

Brief Summary

To examine the effects of a 1-year cluster-randomized controlled intervention of MIND diet on cognitive function among 240 participants with mild cognitive function (MCI) aged 50 years and above from 4 communities.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: MIND diet education
  • Behavioral: Routine follow-up and general advice
N/A

Detailed Description

The current study is a 1-year cluster-randomized controlled intervention trial designed to examine whether the a localized modified Mediterranean-Dietary Approaches to Stop Hypertension (DASH) dietary intervention for neurodegenerative delay (MIND) diet will improve cognitive function among 240 participants with MCI from 4 communities. The modified MIND diet recommends 11 brain healthy food groups (green leafy vegetables, dark red and yellow vegetables, other vegetables, nuts, berries, beans, whole grains, seafood, poultry, olive/tea-seed oil and green tea) and limits intake of 4 unhealthy food groups (red meat and products, animal oil, pastries and sweets, and fried/fast food). This study will randomly assign 240 MCI participants to two groups: A) MIND diet intervention group and B) control group, and estimate the cognitive and biological impacts of the 1-year intervention.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
240 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
Single (outcomes assessor)
Primary Purpose:
Prevention
Official Title:
Effect of MIND Diet Intervention on Cognitive Function in Adults With Mild Cognitive Impairment
Actual Study Start Date :
Jul 26, 2023
Anticipated Primary Completion Date :
Aug 1, 2025
Anticipated Study Completion Date :
Aug 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: MIND diet intervention

Participants in the MIND diet group will receive an education program on a localized MIND diet for 1-year, and will be routinely followed up and given advice on other healthy lifestyles.

Behavioral: MIND diet education
An intensified education program following a localized modified MIND diet for 1 year, which recommends 11 brain healthy food groups (green leafy vegetables, dark red and yellow vegetables, other vegetables, nuts, berries, beans, whole grains, seafood, poultry, olive/tea-seed oil and green tea) and limits intake of 4 unhealthy food groups (red meat and products, animal oil, pastries and sweets, and fried/fast food).

Behavioral: Routine follow-up and general advice
Routine follow-up administered by trained staff.

Active Comparator: Control group

Participants in the control group will be routinely followed up and given general advice on healthy lifestyle.

Behavioral: Routine follow-up and general advice
Routine follow-up administered by trained staff.

Outcome Measures

Primary Outcome Measures

  1. Change in Global Cognition measured by comprehensive Neuropsychological Test Battery (NTB) [Up to one year]

    Global cognitive performance (composite z-score) measured by comprehensive Neuropsychological Test Battery (NTB). The z-score calculation will use the population mean and standard deviation, and a higher z-score indicates better cognitive performance.

  2. Change in Domain-specific Cognition [Up to one year]

    NTB domain-specific cognitive performance (composite z-score) for memory, executive function, attention, language, visuomotor speed and visuoconstruction. The z-score calculation will use the population mean and standard deviation, and a higher z-score indicates better cognitive performance.

Secondary Outcome Measures

  1. Change in Clinical Dementia Rating-Sum of Boxes (CDR-SB) [Up to one year]

    The Clinical Dementia Rating-Sum of Boxes (CDR-SB) is scored from 0 to 18. Higher scores reflect worse performance.

  2. Change in Alzheimer's Disease Cooperative Study Activities of Daily Living Mild Cognitive Impairment-Activities of Daily Living Inventory (ADCS MCI-ADL) [Up to one year]

    The Alzheimer's Disease Cooperative Study Activities of Daily Living-Mild Cognitive Impairment-Activities of Daily Living Inventory (ADCS MCI-ADL) is scored from 0 to 53. Higher scores reflect better performance.

  3. Change in Pittsburgh Sleep Quality Index (PSQI) [Up to one year]

    The Pittsburgh Sleep Quality Index (PSQI) is scored from 0 to 21. Higher scores indicate worse sleep quality.

  4. Change in Montreal Cognitive Assessment (MoCA) score [Up to one year]

    MoCA will be assessed to determine cognitive change.

Other Outcome Measures

  1. Change in dietary behaviour measured using a food frequency questionnaire [Up to one year]

    To evaluate the behavioural effect of dietary changes of the MIND diet intervention package. Exploratory aim 1b: Changes in plasma levels of carotenoids, fatty acids, and vitamins (including folic acid). To evaluate the effect on nutritional biomarkers of the MIND diet intervention.

  2. Change in depressive status measured using the Geriatric Depression Scale (GDS) [Up to one year]

    To evaluate the effect on the depressive status of the MIND diet intervention. A higher GDS score indicates more severe depressive symptoms.

  3. Change in anxiety status measured using the General Anxiety Disorder-7 (GAD-7) [Up to one year]

    To evaluate the effect on the anxiety status of the MIND diet intervention. A higher GAD-7 score indicates more severe anxious symptoms.

  4. Changes in plasma metabolic profiles measured using metabolome analysis [Up to one year]

    To evaluate the effect on plasma metabolites of the MIND diet intervention. We will assay the metabolome using liquid chromatography-mass spectrometry (LC-MS) and construct an overall metabolic score of the diet as the outcome.

  5. Changes in plasma inflammatory biomarkers [Up to one year]

    To evaluate the effect on systematic inflammation of the MIND diet intervention. We will assay interferon-γ, Interleukin (IL)-10, IL-12p70, IL-13, IL-1β, IL-2, IL-4, IL-6, IL-8, Tumor Necrosis Factor alpha, and C-Reaction Protein and construct an overall plasma inflammatory biomarker score as the outcome.

  6. Changes in the intestinal microbiome [Up to one year]

    To evaluate the effect on intestinal microbiome biodiversity and abundance in specific species in faecal samples of the MIND diet intervention. We will assay microbiome using 16-S ribosomal RNA (rRNA) sequencing and construct an overall intestinal microbiome score as the outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • At risk of cognitive decline: cognitive performance at the mean level or slightly lower than expected for age with no dementia (AD8>=3 and/or 5-min MoCA < 11)

  • Free of physical disabilities that preclude participation in the study

  • Willing to complete all study-related activities for 24 months

  • Willing to be randomized to either intervention group

Exclusion Criteria:
  • Allergic to more than one type of food (nuts, berries, olive oil, or fish)

  • Diagnosed of dementia, severe diabetes mellitus, cardiovascular disease, cancer, thyroid disease, kidney disease, or liver disease

  • Diagnosed of major depression or other neuropsychological diseases

  • Severe loss of vision, hearing or communicative ability

  • Substance abuse within 6 months or heavy alcohol consumption (> 2 drinks/day for women; > 3 drinks/day for men).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Zhejiang University School of Medicine Hangzhou Zhejiang China 310058

Sponsors and Collaborators

  • Zhejiang University

Investigators

  • Study Chair: Changzheng Yuan, ScD, Zhejiang University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Changzheng Yuan, Professor, Zhejiang University
ClinicalTrials.gov Identifier:
NCT05975723
Other Study ID Numbers:
  • AARG-22-928604
First Posted:
Aug 4, 2023
Last Update Posted:
Aug 4, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 4, 2023