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Oriental Intervention for Enhanced Neurocognitive Health (Orient) Diet in Populations With High Risk of Stroke (ENDS)

Primary Purpose

High Risk of Stroke

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Usual Diet advice
ORIENT diet intervention
Sponsored by
Second Affiliated Hospital, School of Medicine, Zhejiang University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for High Risk of Stroke focused on measuring stroke, Brain functional network connectivity

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients aged ≥ 40 years High risk of stroke (with ≥ 3 of 8 stroke risk factors, including hypertension, dyslipidemia, diabetes, atrial fibrillation or valvular heart disease, smoking history, obvious overweight or obesity, lack of exercise, family history of stroke, or with transient ischemic attack) Written informed consent available Willingness to complete all assessments and participate in follow-up Adequate Visual and auditory acuity to undergo neuropsychological testing Exclusion Criteria: Nuts, berries, olive oil, or fish allergies previously diagnosed dementia Suspected dementia after clinical assessment by study physician at screening visit Previous history of major head trauma and any intracranial surgery Intracranial abnormalities, such as intracerebral hemorrhage, subarachnoid hemorrhage and other space occupying lesions Extrapyramidal symptoms or mental illness which may affect neuropsychological measurement Severe loss of vision, hearing, or communicative ability Patients presenting a malignant disease with life expectancy < 3 years Participation in an ongoing investigational drug study Any MRI contraindications Exit Criteria: Not meet the inclusion criteria For any poor adherence, not comply with the requirements of the follow-up, or safety reasons determined by investigator Any adverse or serious adverse events during the study period judged by Investigator

Sites / Locations

  • Second Affilated Hospital of Zhejiang University, School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Usual diet advice

ORIENT diet intervention

Arm Description

Outcomes

Primary Outcome Measures

Changes in brain functional network connectivity assessed by resting state functional magnetic resonance imaging (fMRI)
Primary Outcome

Secondary Outcome Measures

Changes in brain functional network efficiency assessed by resting state fMRI
long-term secondary outcome
Changes in brain functional network activity intensity assessed by resting state fMRI
long-term secondary outcome
Changes in brain functional network efficiency assessed by resting state fMRI
long-term secondary outcome
Changes in brain functional network activity intensity assessed by resting state fMRI
long-term secondary outcome
Changes in brain functional network efficiency assessed by resting state fMRI
short-term secondary outcome
Changes in brain functional network activity intensity assessed by resting state fMRI
short-term secondary outcome
Changes in brain functional network connectivity assessed by resting state fMRI
long-term secondary outcome
Changes in brain functional network connectivity assessed by resting state fMRI
long-term secondary outcome
Global cognitive function change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
short-term secondary outcome
Global cognitive function change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
long-term secondary outcome
Global cognitive function change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
long-term secondary outcome
Cognitive domain change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
short-term secondary outcome
Cognitive domain change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
long-term secondary outcome
Cognitive domain change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
long-term secondary outcome
Cognitive function change assessed with Mini-Mental State Examination (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
short-term secondary outcome
Cognitive function change assessed with Mini-Mental State Examination (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
long-term secondary outcome
Cognitive function change assessed with Mini-Mental State Examination (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
long-term secondary outcome
Cognitive function change assessed by Montreal Cognitive Assessment (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
short-term secondary outcome
Cognitive function change assessed by Montreal Cognitive Assessment (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
long-term secondary outcome
Cognitive function change assessed by Montreal Cognitive Assessment (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
long-term secondary outcome
Changes in white matter hyperintensity (WMH) assessed on MRI with T2-Fluid-Attenuated-Inversion-Recovery (FLAIR) sequence
short-term secondary outcome
Changes in lacunes assessed on MRI with T2 FLAIR sequence
short-term secondary outcome
Changes in perivascular spaces assessed on MRI with T2 FLAIR sequence
short-term secondary outcome
Changes in microbleeds assessed on MRI with Susceptibility Weighted Imaging (SWI) sequence sequence
short-term secondary outcome
Changes in brain atrophy (width of the sulci greater than 5mm) assessed on MRI
short-term secondary outcome
Changes in white matter hyperintensity (WMH) assessed on MRI with T2 FLAIR sequence
long-term secondary outcome
Changes in white matter hyperintensity (WMH) assessed on MRI with T2 FLAIR sequence
long-term secondary outcome
Changes in lacunes assessed on MRI with T2 FLAIR sequence
long-term secondary outcome
Changes in lacunes assessed on MRI with T2 FLAIR sequence
long-term secondary outcome
Changes in perivascular spaces assessed on MRI with T2 FLAIR sequence
long-term secondary outcome
Changes in perivascular spaces assessed on MRI with T2 FLAIR sequence
long-term secondary outcome
Changes in microbleeds assessed on MRI with SWI sequence sequence
long-term secondary outcome
Changes in microbleeds assessed on MRI with SWI sequence sequence
long-term secondary outcome
Changes in brain atrophy (width of the sulci greater than 5mm) assessed on MRI
long-term secondary outcome
Changes in brain atrophy (width of the sulci greater than 5mm) assessed on MRI
long-term secondary outcome
Changes in cerebral glymphatic function assessed by non-invasive diffusion tensor image analysis along the perivascular space (ALPS-index)
short-term secondary outcome
Changes in cerebral glymphatic function assessed by non-invasive diffusion tensor image analysis along the perivascular space (ALPS-index)
long-term secondary outcome
Changes in cerebral glymphatic function assessed by non-invasive diffusion tensor image analysis along the perivascular space (ALPS-index)
long-term secondary outcome
Changes in cerebral blood flow (CBF) in the territory of the culprit artery assessed by arterial spin labeling (ASL) perfusion image
short-term secondary outcome
Changes in cerebral blood flow (CBF) in the territory of the culprit artery assessed by arterial spin labeling (ASL) perfusion image
long-term secondary outcome
Changes in cerebral blood flow (CBF) in the territory of the culprit artery assessed by arterial spin labeling (ASL) perfusion image
long-term secondary outcome
Metabolite profiles in participants' faecal samples and serum samples
short-term secondary outcome: metabolite composition was analyzed via liquid chromatography tandem mass spectrometry (LC-MS/MS)
Metabolite profiles in participants' faecal samples and serum samples
long-term secondary outcome: metabolite composition was analyzed via liquid chromatography tandem mass spectrometry (LC-MS/MS)
Incidence of stroke event including ischemic and hemorrhagic stroke
short-term secondary outcome
Incidence of stroke event including ischemic and hemorrhagic stroke
long-term secondary outcome
Incidence of stroke event including ischemic and hemorrhagic stroke
long-term secondary outcome
Change in the Oriental Intervention for Enhanced Neurocognitive Health (ORIENT) diet scale (minimum value = 0, maximum value = 14, and higher scores mean a better outcome)
short-term secondary outcome
Change in the Mediterranean-DASH Diet Intervention for Neurodegenerative Delay (MIND) diet scale (minimum value = 0, maximum value = 15, and higher scores mean a better outcome)
short-term secondary outcome

Full Information

First Posted
September 11, 2023
Last Updated
October 19, 2023
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
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1. Study Identification

Unique Protocol Identification Number
NCT06098235
Brief Title
Oriental Intervention for Enhanced Neurocognitive Health (Orient) Diet in Populations With High Risk of Stroke (ENDS)
Official Title
Oriental Intervention for Enhanced Neurocognitive Health (Orient) Diet in Populations With High Risk of Stroke (ENDS): a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 1, 2023 (Anticipated)
Primary Completion Date
November 1, 2025 (Anticipated)
Study Completion Date
June 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This randomized controlled trial will enroll 160 individuals aged over 40 without dementia who are at high risk of stroke, collecting multi-modal MRI imaging, serum, and fecal samples to investigate the impact of the ORIENT diet on brain functional networks.
Detailed Description
Oriental Intervention for Enhanced Neurocognitive Health (ORIENT) Diet in Populations with High Risk of Stroke is designed to test the impact of a 6-month intervention utilizing a culturally adapted version of the MIND diet, named as the ORIENT diet, on 160 participants (aged 40 years and above, and without dementia) with high risk of stroke (defined as having transient ischemic attack or having ≥ 3 stroke risk factors including hypertension, dyslipidemia, diabetes, atrial fibrillation or valvular heart disease, smoking history, obvious overweight or obesity, lack of exercise, family history of stroke). The ORIENT diet retains the core components of the DASH, Mediterranean, and MIND diets, but incorporates adjustments according to evidence derived from Asian prospective cohorts and Chinese dietary practices. Participants in the intervention group will receive the ORIENT diet intervention, while participants in the control group will receive standard low-sodium and low-fat dietary advice. The study's primary objective is to assess the impact of the ORIENT diet on the brain functional networks of individual with high risk of stroke. The investigation will explore potential mediators and modifiers of the intervention's effects by collecting various cardiovascular risk factors, serum samples, fecal samples, neuropsychological assessment results, and multi-modal magnetic resonance imaging at baseline, 6 months, and 2 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
High Risk of Stroke
Keywords
stroke, Brain functional network connectivity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Usual diet advice
Arm Type
Placebo Comparator
Arm Title
ORIENT diet intervention
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Usual Diet advice
Intervention Description
The usual diet advice include recommendations in guidelines, such as reducing salt and fat intake.
Intervention Type
Behavioral
Intervention Name(s)
ORIENT diet intervention
Intervention Description
The ORIENT diet has the same basic components of the Dietary Approaches to Stop Hypertension (DASH), Mediterranean and MIND diets, but uniquely adjusting some of components according to the evidence derived from Asian prospective cohorts and the Chinese eating habits.
Primary Outcome Measure Information:
Title
Changes in brain functional network connectivity assessed by resting state functional magnetic resonance imaging (fMRI)
Description
Primary Outcome
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Changes in brain functional network efficiency assessed by resting state fMRI
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in brain functional network activity intensity assessed by resting state fMRI
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in brain functional network efficiency assessed by resting state fMRI
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in brain functional network activity intensity assessed by resting state fMRI
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in brain functional network efficiency assessed by resting state fMRI
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in brain functional network activity intensity assessed by resting state fMRI
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in brain functional network connectivity assessed by resting state fMRI
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in brain functional network connectivity assessed by resting state fMRI
Description
long-term secondary outcome
Time Frame
5 years
Title
Global cognitive function change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
Description
short-term secondary outcome
Time Frame
6 months
Title
Global cognitive function change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
Description
long-term secondary outcome
Time Frame
2 years
Title
Global cognitive function change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
Description
long-term secondary outcome
Time Frame
5 years
Title
Cognitive domain change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
Description
short-term secondary outcome
Time Frame
6 months
Title
Cognitive domain change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
Description
long-term secondary outcome
Time Frame
2 years
Title
Cognitive domain change assessed with Z-score of a modified National Institute of Neurological Disorders and Stroke and Canadian Stroke Network-Canadian Stroke Network (NINDS-CSN) protocol (higher scores mean a better outcome)
Description
long-term secondary outcome
Time Frame
5 years
Title
Cognitive function change assessed with Mini-Mental State Examination (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
Description
short-term secondary outcome
Time Frame
6 months
Title
Cognitive function change assessed with Mini-Mental State Examination (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
Description
long-term secondary outcome
Time Frame
2 years
Title
Cognitive function change assessed with Mini-Mental State Examination (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
Description
long-term secondary outcome
Time Frame
5 years
Title
Cognitive function change assessed by Montreal Cognitive Assessment (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
Description
short-term secondary outcome
Time Frame
6 months
Title
Cognitive function change assessed by Montreal Cognitive Assessment (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
Description
long-term secondary outcome
Time Frame
2 years
Title
Cognitive function change assessed by Montreal Cognitive Assessment (minimum value = 0, maximum value = 30, and higher scores mean a better outcome)
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in white matter hyperintensity (WMH) assessed on MRI with T2-Fluid-Attenuated-Inversion-Recovery (FLAIR) sequence
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in lacunes assessed on MRI with T2 FLAIR sequence
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in perivascular spaces assessed on MRI with T2 FLAIR sequence
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in microbleeds assessed on MRI with Susceptibility Weighted Imaging (SWI) sequence sequence
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in brain atrophy (width of the sulci greater than 5mm) assessed on MRI
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in white matter hyperintensity (WMH) assessed on MRI with T2 FLAIR sequence
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in white matter hyperintensity (WMH) assessed on MRI with T2 FLAIR sequence
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in lacunes assessed on MRI with T2 FLAIR sequence
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in lacunes assessed on MRI with T2 FLAIR sequence
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in perivascular spaces assessed on MRI with T2 FLAIR sequence
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in perivascular spaces assessed on MRI with T2 FLAIR sequence
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in microbleeds assessed on MRI with SWI sequence sequence
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in microbleeds assessed on MRI with SWI sequence sequence
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in brain atrophy (width of the sulci greater than 5mm) assessed on MRI
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in brain atrophy (width of the sulci greater than 5mm) assessed on MRI
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in cerebral glymphatic function assessed by non-invasive diffusion tensor image analysis along the perivascular space (ALPS-index)
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in cerebral glymphatic function assessed by non-invasive diffusion tensor image analysis along the perivascular space (ALPS-index)
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in cerebral glymphatic function assessed by non-invasive diffusion tensor image analysis along the perivascular space (ALPS-index)
Description
long-term secondary outcome
Time Frame
5 years
Title
Changes in cerebral blood flow (CBF) in the territory of the culprit artery assessed by arterial spin labeling (ASL) perfusion image
Description
short-term secondary outcome
Time Frame
6 months
Title
Changes in cerebral blood flow (CBF) in the territory of the culprit artery assessed by arterial spin labeling (ASL) perfusion image
Description
long-term secondary outcome
Time Frame
2 years
Title
Changes in cerebral blood flow (CBF) in the territory of the culprit artery assessed by arterial spin labeling (ASL) perfusion image
Description
long-term secondary outcome
Time Frame
5 years
Title
Metabolite profiles in participants' faecal samples and serum samples
Description
short-term secondary outcome: metabolite composition was analyzed via liquid chromatography tandem mass spectrometry (LC-MS/MS)
Time Frame
6 months
Title
Metabolite profiles in participants' faecal samples and serum samples
Description
long-term secondary outcome: metabolite composition was analyzed via liquid chromatography tandem mass spectrometry (LC-MS/MS)
Time Frame
2 years
Title
Incidence of stroke event including ischemic and hemorrhagic stroke
Description
short-term secondary outcome
Time Frame
6 months
Title
Incidence of stroke event including ischemic and hemorrhagic stroke
Description
long-term secondary outcome
Time Frame
2 years
Title
Incidence of stroke event including ischemic and hemorrhagic stroke
Description
long-term secondary outcome
Time Frame
5 years
Title
Change in the Oriental Intervention for Enhanced Neurocognitive Health (ORIENT) diet scale (minimum value = 0, maximum value = 14, and higher scores mean a better outcome)
Description
short-term secondary outcome
Time Frame
6 months
Title
Change in the Mediterranean-DASH Diet Intervention for Neurodegenerative Delay (MIND) diet scale (minimum value = 0, maximum value = 15, and higher scores mean a better outcome)
Description
short-term secondary outcome
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged ≥ 40 years High risk of stroke (with ≥ 3 of 8 stroke risk factors, including hypertension, dyslipidemia, diabetes, atrial fibrillation or valvular heart disease, smoking history, obvious overweight or obesity, lack of exercise, family history of stroke, or with transient ischemic attack) Written informed consent available Willingness to complete all assessments and participate in follow-up Adequate Visual and auditory acuity to undergo neuropsychological testing Exclusion Criteria: Nuts, berries, olive oil, or fish allergies previously diagnosed dementia Suspected dementia after clinical assessment by study physician at screening visit Previous history of major head trauma and any intracranial surgery Intracranial abnormalities, such as intracerebral hemorrhage, subarachnoid hemorrhage and other space occupying lesions Extrapyramidal symptoms or mental illness which may affect neuropsychological measurement Severe loss of vision, hearing, or communicative ability Patients presenting a malignant disease with life expectancy < 3 years Participation in an ongoing investigational drug study Any MRI contraindications Exit Criteria: Not meet the inclusion criteria For any poor adherence, not comply with the requirements of the follow-up, or safety reasons determined by investigator Any adverse or serious adverse events during the study period judged by Investigator
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Min Lou, PhD, MD
Phone
13958007213
Email
lm99@zju.edu.cn
Facility Information:
Facility Name
Second Affilated Hospital of Zhejiang University, School of Medicine
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310009
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Min Lou, PhD, MD
Phone
13958007213
Email
lm99@zju.edu.cn

12. IPD Sharing Statement

Plan to Share IPD
No

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Oriental Intervention for Enhanced Neurocognitive Health (Orient) Diet in Populations With High Risk of Stroke (ENDS)

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