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NCT Number: NCT05887674

Shanghai Non-pharmacological Intervention for Mild Cognitive Impairment and Mild Alzheimer's Disease

This study is a multicentre, randomized, double-blind, controlled trial that aims to investigate the efficacy of multi-domain life-style intervention including low inflammatory-index diet, exercise, and cognitive training in patients with mild cognitive impairment and mild Alzheimer's disease.

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Key information

Age range

60 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

This is a multicentre, randomized, double-blind, controlled trial that aims to investigate the efficacy of multi-domain life-style intervention including low inflammatory-index diet, exercise, and cognitive training in patients with mild cognitive impairment and mild Alzheimer's disease. Patients who eligible to the inclusion criteria and ineligible to the exclusion criteria will be randomly assigned into three groups by a 1:1:1 ratio. Patients in first arm will receive multi-domain life-style intervention including low inflammatory-index diet, exercise, and cognitive training. Patients in the second arm will receive intervention of exercise and cognitive training. Patients in the third arm will receive regular health advice. We hypothesize that the multi-domain intervention will reduce impairment in the study group compared to the control group during the 2-year intervention period.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Aged 60-90 years
  • In accordance with the diagnostic criteria for "mild cognitive impairment due to Alzheimer's disease" or "mild Alzheimer's disease" from the National Institutes of Health National Institute on Aging-Alzheimer's Association (NIA-AA) (2011)
  • The Hamilton depression rating scale/17 edition (HAMD) total score≤10
  • Neurological examination: no obvious signs
  • Education: primary school (grade 6) or above and capacity to complete tests for cognitive ability
  • Capacity to give consent

Exclusion criteria

  • Other causes of cognitive decline: cerebrovascular disease, central nervous system infection, Creutzfeldt-Jakob disease, Huntington's and Parkinson's disease, Creutzfeldt-Jakob disease, traumatic brain dementia, other physical and chemical factors (such as drugs, alcohol, CO), systemic disease (hepatic encephalopathy, pulmonary encephalopathy, etc.), intracranial occupation (a subdural hematoma, brain tumor), the endocrine system disease (thyroid disease, parathyroid disease), and vitamins deficiency or any other causes of dementia
  • The history of nervous system diseases, including stroke, optic myelitis, Parkinson's disease, epilepsy, etc
  • Psychiatric patients, including schizophrenia or other mental illnesses, bipolar disorder, major depression, or delirium
  • There are unstable or serious heart, lung, liver, kidney, endocrine, and hematopoietic system diseases, or Poor prognosis because of malignant diseases such as tumors.
  • Vision or hearing problems that lead to poor performance on cognitive tests
  • Two years history of severe alcoholism, and drug abuse
  • Participants who participated in any other trial 30 days prior to their screening visit
  • Contraindication of MRI scanning
  • Special requirements for diet, e.g., allergy to common food or on a special diet due to medical needs
  • Participants who cannot be followed for at least 6 months (due to a health situation or migration)

Treatment and study plan

diet intervention

Behavioral

Low inflammatory-index diet

Exercise

Behavioral

Guided muscle strength training and stretching exercises

Cognitive training

Behavioral

Cognitive training will be implemented in person

Primary outcomes

  1. Change from baseline global cognitive function at one year

    Time frame: One year

    Change from baseline general cognitive performance at one year assessed by Mini-mental state examination (MMSE)

  2. Change from baseline memory at one year

    Time frame: One year

    Change from baseline verbal memory using the Auditory verbal learning test (AVLT)

  3. Change from baseline visual spatial ability and visual memory at one year

    Time frame: One year

    Change from baseline visual spatial ability and visual memoryevaluated by the Rey-Osterrieth complex figure test (CFT)

Secondary outcomes

  1. Changes in cognition assessed by Clock drawing test, Symbol-digit test, Trail making test, Boston naming test and Language fluency test

    Time frame: One year

    Executive function

  2. Changes in hippocampus related neural circuit-specific resting-state connectivity (FC)

    Time frame: One year

    Neural connectivity by functional MRI

  3. Changes in structural brain MRI including volume of hippocampus and other specific brain regions

    Time frame: One year

    Brain structure by MRI

  4. Changes in Inflammatory biomarkers

    Time frame: One year

    Serum interleukins and tumor necrosis factors

  5. Changes in gut microbiota

    Time frame: One year

    Number of genera and abundance of microbiota in feces and blood

  6. Changes in Metabolic biomarkers

    Time frame: One year

    Low-density lipoprotein, high-density lipoprotein, and total cholesterol

Study contacts

Contact information is provided by the study sponsor or research team.

Binyin Li, Dr

CONTACT

[email protected]

021-64370045

Sponsors and collaborators

Lead sponsor

Ruijin Hospital

Other

Collaborators

  • Shanghai Sinopharm Nursing Care Center

Registry information

Official study title

Shanghai Non-pharmacological Intervention for Mild Cognitive Impairment and Mild Alzheimer's Disease: Combined Low Inflammatory-index Diet, Physical Exercises, and Cognitive Training in Nursing Home

Acronym: SIM-2

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jun 5, 2023
Registry last updated
Nov 22, 2024

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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