NCT05374005

Brief Summary

Sporadic cerebral small vessel disease (CSVD) is not only the most common subtype of vascular dementia, in recent multi-center study showed that sporadic CSVD harbors in a third of Alzheimer's disease (AD) patients in 9 Asian regions. The CSVD increases the severity of cognitive impairment in these patients and has an etiological contribution to the development of AD. Studies demonstrated that CSVD is more prevalent in Chinese than in Australians and this association was independent of traditional vascular risk factors (e.g. hypertension). Other factors such as lifestyle, environmental or genetic factors may explain this difference. Although hypertension is an important cause for CSVD, it only accounts for a small proportion of the variance in CSVD. Irrespective of the cause, it is currently believed that endothelial dysfunction of CSVD is the key pathophysiological mechanism of CSVD. Having an effective treatment of CSVD will have an enormous impact on the prevention of dementia. Excessive dietary sodium is an established risk factor for cardiovascular diseases, including stroke. It is traditionally linked to its effects in raising blood pressure. The Department of Health advocated reducing salt intake for the prevention of hypertension, coronary heart disease, and stroke. However, recent epidemiological studies suggest that it may have a direct effect on cardiovascular diseases independent of blood pressure. A recent animal study showed that excessive dietary sodium-induced cerebral endothelial dysfunction, resulting in cognitive impairment. Interestingly, endothelial dysfunction was related to an adaptive immune response in the gut. A clinical study conducted in the United Kingdom suggested excessive dietary sodium intake may promote CSVD A clinical study conducted in the United Kingdom suggested excessive dietary sodium intake may promote CSVD by increasing WMH volume in the brain, independent of its effects on blood pressure. Notably, a few animal studies showed that the association between high dietary sodium and worse cognitive function in the absence of blood pressure changes. This pinpoints the important role of dietary sodium as an independent contributor to brain health and cognition. This study aims to assess the association between dietary sodium, neuroimaging measures, and cognition in cerebral small vessel disease and controls during the 18-month follow-up.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
220

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 10, 2022

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 13, 2022

Completed
1 month until next milestone

Study Start

First participant enrolled

June 22, 2022

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2025

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2025

Completed
Last Updated

February 15, 2024

Status Verified

February 1, 2024

Enrollment Period

2.9 years

First QC Date

May 10, 2022

Last Update Submit

February 13, 2024

Conditions

Keywords

CSVD

Outcome Measures

Primary Outcomes (15)

  • Change of level of urinary sodium

    24 hours of urine will be collected to measure the level of sodium The higher the sodium level the worse the outcome

    Baseline and 18 month

  • Change of Gait

    Gait velocity will be assessed using the 8-meter walking time. Time for walking 8-m will be measured by a stopwatch. The faster of two trials will be used in the analysis The faster of the walking time the better outcome.

    Baseline and 18 month

  • Change of balance

    Single leg stance time will be measured by asking participants, with their hands on their hips, to balance as long as possible on one leg with an upper limit of 30 seconds. Two trials for each leg will be performed. The best time of the four trials will be used for analysis. The longer the time duration the better outcome.

    Baseline and 18 month

  • Change of Hong Kong MOntreal Cognitive Assessment

    Hong Kong MOntreal Cognitive Assessment (HK-MoCA) is a cognitive assessmenttool. Score from 0 to 30 . The lower score reflect the worse the outcome.

    Baseline and 18 month

  • Change of The Chinese Geriatric Depression Scale 30

    The Chinese Geriatric Depression Scale is used to detect depressive mood. Score 0 to 30. The higher the score, the worse the outcome

    Baseline and 18 month

  • Change of Pittsburgh sleep quality index

    Pittsburgh sleep quality index Chinese Version is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The questionnaire contains frequency questions related to sleep quality, each question scale from 0 to 3. The higher the score, the worse the outcome. There is no total score available for this assessment

    Baseline and 18 month

  • Change of Hong Kong List Learning Test

    Hong Kong List Learning Test is memory test in Chinese designed for the assessment of the processes and organizational strategies involved in learning verbal information. The more negative the standard deviation the worse the outcome

    Baseline and 18 month

  • Food frequency questionnaire

    The food frequency questionnaire serves the purpose of understanding the type of food that subject frequently consume in the past 12 months. There is no total score for this assessment. There is no positive and negative outcome available

    Baseline

  • Food frequency questionnaire

    The food frequency questionnaire serves the purpose of understanding the type of food that subject frequently consume in the past 12 months. There is no total score for this assessment. There is no positive and negative outcome available

    18 month

  • 24 hour food intake

    The 24 hour food intake serves the purpose of understanding the food that subject consume on the day of urine collection There is no positive and negative outcome available

    Baseline

  • 24 hour food intake

    The 24 hour food intake serves the purpose of understanding the food that subject consume on the day of urine collection There is no positive and negative outcome available

    18 Month

  • Change of creatinine in urine

    24 hours of urine will be collected to measure the level of creatinine The higher the creatinine level the worse the outcome

    Baseline and 18 month

  • change of urinary potassium

    24 hours of urine will be collected to measure the level of potassium The higher the potassium level the worse the outcome

    Baseline and 18 month

  • Change of International Physical Activity Questionnaire

    the International Physical Activity Questionnaire is a self report assessment to investigate the daily activities (frequency, duration, and level) of subject within the 7 days prior assessment There is no total score available for this questionnaire. The higher duration and frequency and level of daily activities the better outcome

    Baseline and 18 month

  • Change of Brain Peak Width of Skeletonized Mean Diffusivity

    Peak Width of Skeletonized Mean Diffusivity is a robust, fully-automated and easy-to-implement marker for cerebral small vessel disease based on diffusion tensor imaging, white matter tract skeletonization and histogram analysis. It is a biomarker for brain MRI images.

    Baseline and 18 month

Secondary Outcomes (1)

  • Change of 24 hour blood pressure monitoring

    Baseline and 18 Month

Eligibility Criteria

Age55 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Subject with cSVD will be recruited at stroke unit and neurology clinic at Prince of Wales Hospital. Healthy volunteers will recruited through other community cohorts.

You may qualify if:

  • Chinese ethnicity,
  • age between 55 and 80-year-old, and
  • a primary language of Cantonese.
  • Age-Related White Matter Change (ARWMC) Scale of 2 or early 3 in FLAIR MRI;
  • Modified Functional Ambulation Classification 5 or above;
  • Montreal Cognitive Assessment (MoCA) score \< 25;

You may not qualify if:

  • Hypernatremia (Na \>146mmol/L) or hyponatremia (Na \<134 mmol/L) from screening blood test;
  • With sodium supplement;
  • Renal failure (stage 4 \& 5) with glomerular filtration rate \< 29;
  • performed cardiac surgery or neurosurgery, with cardiac failure;
  • Had major psychiatric diseases
  • Contraindications for MRI.
  • Dementia or MoCA score lower than 2nd percentile of the age and education adjusted cutoff ;
  • Cerebral white matter changes unrelated to neurodegenerative, e.g. CADASIL, X-linked adrenoleukodystrophy, metabolic diseases, multiple sclerosis, etc.\|
  • Contraindication to proposed imaging, e.g. chronic kidney disease (KDNIGO) stage 4 or above, acute kidney injury, hypersensitivity to gadolinium-based contrast, non-MRI conditional implants or prosthesis
  • Medical condition that would not allow the patient to adhere to the protocol or complete the study.;
  • Patient with established neurodegenerative disorders (e.g. Parkinson's Disease, Alzheimer's Disease, etc.);
  • Pregnancy.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Prince of Wales Hospital

Shatin, N.T., 00000, Hong Kong

RECRUITING

MeSH Terms

Conditions

Cerebral Small Vessel Diseases

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Bonnie Yin Ka Lam, PhD

    Chinese University of Hong Kong

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Pauline Kwan, Master

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant Professor

Study Record Dates

First Submitted

May 10, 2022

First Posted

May 13, 2022

Study Start

June 22, 2022

Primary Completion

May 1, 2025

Study Completion

October 30, 2025

Last Updated

February 15, 2024

Record last verified: 2024-02

Data Sharing

IPD Sharing
Will not share

Locations