Diet ModificationMHDNCT03240406
Multicultural Healthy Diet to Reduce Cognitive Decline
A study testing Multicultural Healthy Diet and Usual Diet plus Self-Care in people with Diet Modification and Cognitive Decline, run by Albert Einstein College of Medicine at 1 site in United States.
Trial summary
This is a pilot randomized controlled clinical trial is designed to investigate whether the Multicultural Healthy Diet (MHD), an anti-Inflammatory diet tailored to a multi-cultural population, can improve cognitive functioning in a middle aged (40-65 yr) urban population in Bronx, New York compared to a usual diet. Read more about this study
- Who is it for?
- Ages 40 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Diet Modification, Cognitive Decline, Cognitive Change
- What is being tested?
- Multicultural Healthy Diet and Usual Diet plus Self-Care
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 393 participants
- Where
- 1 siteUnited States
- Study dates
- 2 Oct 2018to 30 Aug 2023
- Phase
- Interventional
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- living, working, attending school or visiting Co-op City, Bronx (e.g. for shopping, doctors' visits, etc.) or communities neighboring Co-op City and between 40-65 yr of age
- willingness to accept assignment to intervention or comparison diet group
- willingness to participate in a study where weight loss is not a primary goal
Who cannot join
- cognitively impaired
- history of traumatic brain injury
- psychiatric illness
- history of diabetes and experiencing hypoglycemia
- liver disease
- uncontrolled hypertension as defined as blood pressure > 140/90 mm Hg
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- history of cardiovascular disease that affects physical functioning
- severe chronic illness
- low literacy
- history of alcohol or drug dependence
- hematologic disease or malignancy not in remission for more than 5 years
- visual, auditory, or motor impairment that precludes cognitive testing.
- chronic kidney disease on dialysis or special diet
Trial locations and contacts
1 site in 1 country.
United States1 site
Albert Einstein College of Medicine
The Bronx, New York, 10461
About this study
Official title: Multicultural Healthy Diet to Reduce Cognitive Decline & Alzheimer's Disease Risk
This is a pilot randomized controlled clinical trial is designed to investigate whether the Multicultural Healthy Diet (MHD), an anti-Inflammatory diet tailored to a multi-cultural population, can improve cognitive functioning in a middle aged (40-65 yr) urban population in Bronx, New York compared to a usual diet.
Read the detailed description
The Multicultural Healthy Diet (MHD) is a pilot randomized controlled clinical trial designed to test the effects of an 18 month intervention on cognitive function among 290 middle-aged individuals (40-65 yr). MHD is an anti-inflammatory diet tailored to a multicultural population. The emphasis of the intervention is on plant-based foods and limited animal and high saturated fat foods with focus on anti-inflammatory foods/food components specific to the cultural context of the participants. The trial will employ a parallel group design comparing the effects of the dietary intervention (MHD) on cognitive status to those of the control diet or usual diet plus modules on self-care matters such as dealing with aches and pains of aging, obtaining a health care proxy ,etc. To show that MHD can be adapted to this population serum biomarkers indicative of the MHD diet pattern such as fatty acid profile as well as other key nutrition biomarkers will be evaluated. Other aims include testing whether the MHD intervention can benefit cognitive function using real-time ambulatory assessments. The investigators will also assess plasma and serum markers of inflammation. Components of the MHD diet that are associated with stable or improved measures of cognition will also be evaluated. The clinical site for the proposed study is at the Albert Einstein College of Medicine; the ambulatory cognitive assessment reading center is at Pennsylvania State University, State College; the statistical core is at the Kaiser Permanente Washington Health Research Institute and the laboratory for biospecimen analysis is at the University of Minnesota.
- Conditions
- Diet Modification, Cognitive Decline, Cognitive Change
- Being tested
- Multicultural Healthy Diet, Usual Diet plus Self-Care
- Medical subject headings
- Cognitive Dysfunction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Multicultural Healthy DietOther
An anti-inflammatory dietary pattern consists of a dietary pattern that has high anti-inflammatory potential
Usual Diet plus Self-CareOther
Usual diet plus sessions that focus on self-care such as dealing with aches and pains of aging.
| Study group | Role | What they receive |
|---|---|---|
| Anti-inflammatory dietary intervention | Active comparator | 18 month intervention of dietary counseling to adhere to the Multicultural Healthy Diet or the anti-inflammatory diet, Receives: Other: Multicultural Healthy Diet |
| Usual Diet plus Self-Care | Placebo comparator | 18 month intervention of usual diet plus self-care modules Receives: Other: Usual Diet plus Self-Care |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Mean Global Composite Cognition Score From Baseline
Change in global composite cognition score (standardized unit) is computed as the average of the three domain-specific Z-scores of the participant's performance on three ambulatory cognitive assessments: visuospatial working memory (Dot Grid Memory), processing speed (Symbol Search), and short-term associative memory binding (Color Shapes Task) at 9 months post baseline (Burst 1). Z-scores are centered at a population mean of "0" (i.e., a Z-score of "0" signifies that the data point(s) is equal to the population mean at study baseline for all three tasks in the composite average; positive Z-score group values indicate the number of standard deviations the data point(s) is above the mean and negative Z-score group values indicate the number of standard deviations the data point(s) is below the mean). Mean change in global composite Z-score from baseline will be reported by study arm. Increase in composite Z-scores from baseline are associated with improved cognition.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Secondary outcomes (40)
Dietary Inflammatory Index (DII) Score
DII score was determined by an algorithm that summarized the inflammatory potential of the diet. The DII score represents a weighted sum of the self-reported quantities of 28 foods, each translated into Z-scores using a global comparative database consisting of data from 11 countries by subtracting from the individual's self-report value the mean of the global database, then dividing by the standard deviation (SD). Z-scores are centered at a population mean of "0" (i.e., a Z-score of "0" signifies that the data point(s) is = to the population mean at study baseline for all 3 tasks in the composite average; positive and negative Z-score group values indicate the number of SD the data point(s) is above or below the mean, respectively). For this study, possible scoring range for 28 food parameters was -8 to 8 based on ref: Hebert JR, et.al., Perspective: The Dietary Inflammatory Index (DII®): Adv Nutr. 2019;10:185-95. Higher Z-score values are indicative of a more pro-inflammatory diet.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Energy-Adjusted DII Score
Energy-adjusted DII score was determined by an algorithm that summarized the inflammatory potential of the diet. This score represents a weighted sum of self-reported quantities of 28 foods per 1000 kilocalories of consumption that were then translated into Z-scores using a global comparative database of data from 11 countries by subtracting from the individual's self-report value the mean of the global database, then dividing by the SD. Z-scores are centered at a population mean of 0 (i.e., a Z-score of 0 signifies that the data point is = to the population mean at study baseline for all 3 tasks in the composite average; positive and negative Z-score group values indicate the number of SD the data point is above or below the mean, respectively). For this study, possible scoring range for 28 food parameters was -8 to 8 based on ref: Hebert JR, et.al., Perspective: The Dietary Inflammatory Index (DII®): Adv Nutr. 2019;10:185-95. Higher values are indicative of a more inflammatory diet.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Total Serum Folate Levels
Blood sera specimens were collected and processed at Baseline and 9-months post-intervention and shipped to University of Minnesota Advanced Research \& Diagnostic Laboratory (ARDL) for total folate analysis by a validated serum folate assay. Mean total folate levels are summarized by study arm and reported in nmol/L. The lower limit of detection (LLOD) for mean total folate is 4.54 nmol/L and the upper limit of detection (ULOD) 90.8 nmol/L. Increase in this biomarker from baseline for MHD participants indicates possible adherence to an MHD dietary pattern such as eating more green leafy vegetables.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
α-Tocopherol Levels
Blood plasma specimens were collected and processed at Baseline and 9-months post-intervention and shipped to University of Minnesota ARDL for α-tocopherol analysis by an HPLC method. α-Tocopherols were measured with a diode array detector equipped HPLC system. Mean α-tocopherol levels are summarized by study arm and reported in mcg/mL. There are no reference ranges for this biomarker from this laboratory (other than non-negative values). Increase in this biomarker from baseline for MHD participants indicates possible adherence to an MHD dietary pattern.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
α-Carotenoid Levels
Blood plasma specimens were collected and processed at Baseline and 9-months post-intervention from a sub-sample and shipped to University of Minnesota ARDL lab for α-carotenoid analysis by an HPLC method. α-Carotenoids were measured with a diode array detector equipped HPLC system. Mean α-carotenoid levels are summarized by study arm and reported in mcg/mL. There are no reference ranges for this biomarker (other than non-negative values). Increase in this biomarker from baseline for MHD participants indicates possible adherence to an MHD dietary pattern.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Vitamin B12 Levels
Blood sera specimens were collected and processed at Baseline and 9-months post-intervention and shipped to University of Minnesota ARDL laboratory for Vitamin B12 analysis by a validated Vitamin B12 assay. Mean Vitamin B12 levels are summarized by study arm and reported in pg/mL. Reference ranges for this biomarker are: 232-1245 pg/mL and LLOD is 100 pg/mL. Increase in this biomarker from baseline for MHD participants indicates possible adherence to an MHD dietary pattern.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Fatty Acid Profile
Blood plasma specimens were collected and processed at Baseline and 9-months follow-up for a sub-sample and shipped to University of Minnesota ARDL laboratory for total fatty acid analysis by a gas chromatography method. Fatty acids are expressed as a percent of total fatty acids. Fatty acids are compared with each sample rather than measured against a standard and the range of percentage values for each fatty acid is 0-100%. Mean percentage plasma levels of the following fatty acids will be summarized by study arm for Burst 2: Sum of monounsaturated fatty acids (n=6); Long chain saturated fatty acids (fatty acids with 20 or more carbons (n=3)); EPA (eicosapentaenoic acid); DHA (docosahexaenoic acid); n3 DPA (omega three docosapentaenoic acid).
Monounsaturated fat is a composite of 6 fatty acids: 16:1n7 cis, 17:1n7T, 18:1n9 cis,18:1n7 cis, 20:1n9, and 24:1n9 Long chain saturated fat is a composite of 3 fatty acids: 22:0, 23:0, and 24:0
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Serum Sodium
Serum specimens were collected and processed at Baseline and 9-months follow-up and shipped to University of Minnesota ARDL laboratory for analysis on Roche Cobas 8000 Chemistry Analyzer. Mean serum sodium levels are summarized by study arm and reported in mmol/L. Reference range is 136-145 mmol/L and the lower LOD is 80 mmol/L. Decreased serum sodium levels from baseline may indicate dehydration.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Total Moisture
Total Moisture obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Total moisture from diet was captured by the MOIS variable field within the ASA24. This field is quantified in grams (g) of water. Possible results values are limited to values > 0 (i.e., positive values). Basic descriptive statistics were used to summarize data by arm.ASA-2018 and 2020
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Energy
Energy obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Total energy from diet was captured by the KCAL variable field within the ASA24. This field represents kilocalories (kcal) of energy. Possible results values are to values > 500kcal. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Protein
Protein obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Protein from the diet was captured by the PROT variable field within the ASA24. This field represents grams (g) of protein consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Total Intact Fruits + Fruit Juices
Total Intact fruits and fruit juices obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Total Intact fruit and fruit juice consumption from the diet was captured by the F_TOTAL variable field within the ASA24. This field represents total fruit consumption in cup equivalents (cup eq). Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Dark Green Vegetables
Dark Green Vegetables obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Dark green vegetable consumption from the diet was captured by the V_DRKGR variable field within the ASA24. This field represents dark green vegetable consumption in cup equivalents (cup eq). Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Total Fats
Total fats obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Total fats from the diet, which consisted of total saturated fatty acids, total monounsaturated fatty acids, and total polyunsaturated fatty acids, was captured by the TFAT variable field within the ASA24. This field represents grams (g) of total fats consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Solid Fats
Solid fats obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Solid fats from the diet was captured by the DISCFAT_SOL variable field within the ASA24. This field represents grams (g) of solid fats consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Carbohydrates
Carbohydrates obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Carbohydrates from the diet was captured by the CARB variable field within the ASA24. This field represents grams (g) of carbohydrates consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Total Folate From Food
Total Folate from food obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Total Folate from food was captured by the FF variable field within the ASA24. This field represents micrograms (mcg) of total folate from food consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Non-food Folate
Non-food Folate obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Non-food Folate was captured by the FDFE variable field within the ASA24. This field represents micrograms (mcg) of Non-food Folate consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Vitamin B-12
Vitamin B-12 obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Vitamin B-12 was captured by the VB12 variable field within the ASA24. This field represents micrograms (mcg) of Vitamin B-12 consumed (including supplemental sources). Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Alpha Carotene
Alpha Carotene obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Alpha Carotene from the diet was captured by the ACAR variable field within the ASA24. This field represents micrograms (mcg) of Alpha Carotene consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Beta Carotene
Beta Carotene obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Beta Carotene from the diet was captured by the BCAR variable field within the ASA24. This field represents micrograms (mcg) of Beta Carotene consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Retinol
Retinol obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Retinol from the diet was captured by the RET variable field within the ASA24. This field represents micrograms (mcg) of Retinol consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Beta Cryptoxanthin
Beta Cryptoxanthin obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Beta Cryptoxanthin from the diet was captured by the CRYP variable field within the ASA24. This field represents micrograms (mcg) of Beta Cryptoxanthin consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Lycopene
Lycopene obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Lycopene from the diet was captured by the LYCO variable field within the ASA24. This field represents micrograms (mcg) of Lycopene consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Lutein + Zeaxanthin
Lutein + Zeaxanthin obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Lutein + Zeaxanthin from the diet was captured by the LZ variable field within the ASA24. This field represents micrograms (mcg) of Lutein + Zeaxanthin consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Alpha Tocopherol (Vitamin E)
Alpha Tocopherol (Vitamin E) obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Alpha Tocopherol from the diet was captured by the ATOC variable field within the ASA24. This field represents micrograms (mg) of Alpha Tocopherol consumed (including from supplemental sources). Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Seafood High in n-3 Fatty Acids
Seafood high in n-3 fatty acids obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Seafood high in n-3 fatty acids from the diet was captured by the M_FISH_HI variable field within the ASA24. This field represents ounce equivalents (oz eq) of Seafood high in n-3 fatty acids consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: EPA (P205)
EPA (P205) obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. EPA (P205) from the diet was captured by the P205 variable field within the ASA24. This field represents grams (g) of EPA (P205) consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: DHA (P226)
DHA (P226) obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. DHA (P226) from the diet was captured by the P226 variable field within the ASA24. This field represents grams (g) of DHA (P226) consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: DPA (P225)
DPA (P225) obtained from the participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. DPA (P225) from the diet was captured by the P225 variable field within the ASA24. This field represents grams (g) of DPA (P225) consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Beans and Peas (Legumes)
Beans and peas (Legumes) consumed as part of participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Legumes information from the diet was captured by the V_LEGUMES variable field within the ASA24. This field represents cup equivalents (cup eq) of legumes consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Whole Grains
Whole grains consumed as part of participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Whole grains information from the diet was captured by the G_WHOLE variable field within the ASA24. This field represents ounce equivalents (oz eq) of whole grains consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Cured Meats
Cured meats consumed as part of participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Cured meats information from the diet was captured by the PF_CUREDMEAT variable field within the ASA24. This field represents ounce equivalents (oz eq) of cured meats consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Poultry
Poultry consumed as part of participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Poultry information from the diet was captured by the PF_POULT variable field within the ASA24. This field represents ounce equivalents (oz eq) of poultry consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Nuts and Seeds
Nuts and seeds consumed as part of participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Nuts and seeds information from the diet was captured by the PF_NUTSDS variable field within the ASA24. This field represents ounce equivalents (oz eq) of nuts and seeds consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Cheeses
Cheeses consumed as part of participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Cheese information from the diet was captured by the D_CHEESE variable field within the ASA24. This field represents cup equivalents (cup eq) of cheeses consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Added Sugars
Added sugars consumed as part of participants' diet was derived as a parameter of the self-reported diet components and food groups from the 2018 and 2020 versions of the Automated Self-reported Self-administered 24 hour food records (ASA24-2018 and ASA24-2020) at baseline and 9 month follow-up. Added sugars information from the diet was captured by the ADD_SUGARS variable field within the ASA24. This field represents tablespoon equivalents (tsp eq) of added sugars consumed. Possible results values are limited to non-negative values. Basic descriptive statistics were used to summarize data by arm.
Measured: Baseline (Burst 1) and 9 months (Burst 2)
Symbol Search Task Performance
Symbol Search Task Performance is an ambulatory cognitive assessment of processing speed/attention. The task is administered 5 times daily throughout each 7-day measurement Burst (Baseline, 9 months, 18 months, 27 months). Mean response time in milliseconds (ms) for accurate trials will be determined and reported. Possible values ranges for Symbol Search Task Performance are >0 ms (i.e., positive values). Lower Symbol Search Task Performance values in mean response time are indicative of improvement in cognitive processing.
Measured: Baseline (Burst 1), and 9 months (Burst 2), 18 months (Burst 3), and 27 months (Burst 4) post-intervention
Grid Memory Task Performance
Grid Memory Task Performance is an ambulatory cognitive assessment of visuospatial working memory. The task is administered 5 times daily throughout each 7-day measurement Burst (Baseline, 9 months, 18 months, 27 months). The mean error distance (pixel Euclidean distance, represented in pixels) of the red dots between study and recall arrays will be quantified and reported based on the completion of 4 trials. Possible value ranges for pixels are >0 (i.e., positive values). Lower pixel values are indicative of improved short-term recall and visuospatial working memory.
Measured: Baseline (Burst 1), and 9 months (Burst 2), 18 months (Burst 3), and 27 months (Burst 4) post-intervention
Color Shapes Task Performance
Color Shapes Task Performance is an ambulatory cognitive assessment of short-term associative visual memory. The task is administered 5 times daily throughout each 7-day measurement Burst. The task had 2 conditions, signal present and signal absent. Hit rate represents the proportion of trials where participants correctly responded that signal was present. False alarm rate represents the proportion of trials where a signal was absent where participants incorrectly responded that a signal was present. Corrected Recognition Score represents the overall sensitivity to the signal and is calculated by subtracting the False alarm rate from the Hit rate and is summarized by study arm as described in Hakun, et.al., (2024). Mobile Monitoring of Cognitive Change (M2C2): High-Frequency Assessments and Protocol Reporting Guidelines. Possible ranges for Corrected Recognition Score are -1 to 1. Higher Corrected Recognition Rate values are indicative of better short term associative memory-binding.
Measured: Baseline (Burst 1), and 9 months (Burst 2), 18 months (Burst 3), and 27 months (Burst 4) post-intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Aug 2017
- Study start2 Oct 2018
- Primary completion3 Jul 2023
- Study completion30 Aug 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Diet ModificationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This is a pilot randomized clinical trial to the effects of an anti-inflammatory diet on cognition in a middle-aged cohort. The comparison arm will receive information on self-care matters such as aches and pains of aging.
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 393 participants (actual)
Sponsor and investigators
- Lead sponsor
- Albert Einstein College of Medicine
- Sponsor type
- University, hospital or other
- Collaborators
- Penn State University, Kaiser Permanente, University of Minnesota, National Institute on Aging (NIA), National Center for Advancing Translational Sciences (NCATS)
- Responsible party
- Principal investigator, Yasmin Mossavar-Rahmani, Albert Einstein College of Medicine
- Investigators
- Yasmin Mossavar-Rahmani, Ph.D, RD, Principal investigator, Albert Einstein College of Medicine
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03240406
- Sponsor's protocol ID
- 2016-6613
- Other IDs
- R01AG055527, K99AG056670, UL1TR002556
- Acronym
- MHD
- Status last verified
- Dec 2024
- First submitted
- 1 Aug 2017
- Last updated
- 12 Dec 2024
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Data and specimens will be shared with potential collaborators, after obtaining participant consent, consistent with HIPPA guidelines
Publications
Mossavar-Rahmani Y, Shaw PA, Hakun JG, Katz MJ, Wylie-Rosett J, Sliwinski MJ. Multicultural Healthy Diet to Reduce Cognitive Decline & Alzheimer's Disease Risk: Study protocol for a pilot randomized controlled trial. Contemp Clin Trials. 2023 Jan;124:107006. doi: 10.1016/j.cct.2022.107006. Epub 2022 Nov 14.
PubMed 36396064Mossavar-Rahmani Y, Hyun N, Hakun JG, Katz MJ, Pavlovic JM, Zetterberg H, Wang Z, Yang JB, Wylie-Rosett J, Hebert JR, Sliwinski MJ, Shaw PA. The effects of the Multicultural Healthy Diet on cognitive decline and Alzheimer's disease risk: a phase II randomized controlled trial in middle-aged adults. Am J Clin Nutr. 2025 Jul;122(1):48-59. doi: 10.1016/j.ajcnut.2025.05.011. Epub 2025 May 22.
PubMed 40412481Hakun JG, Benson L, Qiu T, Elbich DB, Katz M, Shaw PA, Sliwinski MJ, Mossavar-Rahmani Y. Cognitive Health Benefits of Everyday Physical Activity in a Diverse Sample of Middle-Aged Adults. Ann Behav Med. 2025 Jan 4;59(1):kaae059. doi: 10.1093/abm/kaae059.
PubMed 39427230
Study at a glance
From the registry record, last updated by the sponsor on 12 Dec 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Multicultural Healthy Diet to Reduce Cognitive Decline & Alzheimer's Disease Risk
- ClinicalTrials.gov ID
- NCT03240406
- Acronym / sponsor ID
- MHD / 2016-6613
- Conditions
- Diet Modification, Cognitive Decline, Cognitive Change
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 393 participants (actual)
- Lead sponsor
- Albert Einstein College of MedicineUniversity, hospital or other
- Collaborators
- Penn State University, Kaiser Permanente, University of Minnesota, National Institute on Aging (NIA), National Center for Advancing Translational Sciences (NCATS)
- Study start
- 2 Oct 2018 (actual)
- Primary completion
- 3 Jul 2023 (actual)
- Study completion
- 30 Aug 2023 (actual)
- First posted
- 7 Aug 2017 (actual)
- Results
- Posted 12 Dec 2024
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a pilot randomized controlled clinical trial is designed to investigate whether the Multicultural Healthy Diet (MHD), an anti-Inflammatory diet tailored to a multi-cultural population, can improve cognitive functioning in a middle aged (40-65 yr) urban population in Bronx, New York compared to a usual diet.
Detailed description
The Multicultural Healthy Diet (MHD) is a pilot randomized controlled clinical trial designed to test the effects of an 18 month intervention on cognitive function among 290 middle-aged individuals (40-65 yr). MHD is an anti-inflammatory diet tailored to a multicultural population. The emphasis of the intervention is on plant-based foods and limited animal and high saturated fat foods with focus on anti-inflammatory foods/food components specific to the cultural context of the participants. The trial will employ a parallel group design comparing the effects of the dietary intervention (MHD) on cognitive status to those of the control diet or usual diet plus modules on self-care matters such as dealing with aches and pains of aging, obtaining a health care proxy ,etc. To show that MHD can be adapted to this population serum biomarkers indicative of the MHD diet pattern such as fatty acid profile as well as other key nutrition biomarkers will be evaluated. Other aims include testing whether the MHD intervention can benefit cognitive function using real-time ambulatory assessments. The investigators will also assess plasma and serum markers of inflammation. Components of the MHD diet that are associated with stable or improved measures of cognition will also be evaluated. The clinical site for the proposed study is at the Albert Einstein College of Medicine; the ambulatory cognitive assessment reading center is at Pennsylvania State University, State College; the statistical core is at the Kaiser Permanente Washington Health Research Institute and the laboratory for biospecimen analysis is at the University of Minnesota.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- Model description
- This is a pilot randomized clinical trial to the effects of an anti-inflammatory diet on cognition in a middle-aged cohort. The comparison arm will receive information on self-care matters such as aches and pains of aging.
| Arm | Type | Receives |
|---|---|---|
| Anti-inflammatory dietary intervention | Active comparator | Other: Multicultural Healthy Diet18 month intervention of dietary counseling to adhere to the Multicultural Healthy Diet or the anti-inflammatory diet, |
| Usual Diet plus Self-Care | Placebo comparator | Other: Usual Diet plus Self-Care18 month intervention of usual diet plus self-care modules |
Who may qualify
- Ages
- 40 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- living, working, attending school or visiting Co-op City, Bronx (e.g. for shopping, doctors' visits, etc.) or communities neighboring Co-op City and between 40-65 yr of age
- willingness to accept assignment to intervention or comparison diet group
- willingness to participate in a study where weight loss is not a primary goal
Key exclusion criteria (13 listed)
- cognitively impaired
- history of traumatic brain injury
- psychiatric illness
- history of diabetes and experiencing hypoglycemia
- liver disease
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Multicultural Healthy DietAn anti-inflammatory dietary pattern consists of a dietary pattern that has high anti-inflammatory potential | Other | Anti-inflammatory dietary intervention |
| Usual Diet plus Self-CareUsual diet plus sessions that focus on self-care such as dealing with aches and pains of aging. | Other | Usual Diet plus Self-Care |
Primary outcome
Change in Mean Global Composite Cognition Score From Baseline
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Change in global composite cognition score (standardized unit) is computed as the average of the three domain-specific Z-scores of the participant's performance on three ambulatory cognitive assessments: visuospatial working memory (Dot Grid Memory), processing speed (Symbol Search), and short-term associative memory binding (Color Shapes Task) at 9 months post baseline (Burst 1). Z-scores are centered at a population mean of "0" (i.e., a Z-score of "0" signifies that the data point(s) is equal to the population mean at study baseline for all three tasks in the composite average; positive Z-score group values indicate the number of standard deviations the data point(s) is above the mean and negative Z-score group values indicate the number of standard deviations the data point(s) is below the mean). Mean change in global composite Z-score from baseline will be reported by study arm. Increase in composite Z-scores from baseline are associated with improved cognition.
40 secondary outcomes
Dietary Inflammatory Index (DII) Score
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Energy-Adjusted DII Score
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Total Serum Folate Levels
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
α-Tocopherol Levels
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
α-Carotenoid Levels
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Vitamin B12 Levels
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Fatty Acid Profile
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Serum Sodium
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Total Moisture
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Energy
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Protein
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Total Intact Fruits + Fruit Juices
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Dark Green Vegetables
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Total Fats
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Solid Fats
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Carbohydrates
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Total Folate From Food
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Non-food Folate
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Vitamin B-12
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Alpha Carotene
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Beta Carotene
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Retinol
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Beta Cryptoxanthin
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Lycopene
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Lutein + Zeaxanthin
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Alpha Tocopherol (Vitamin E)
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Seafood High in n-3 Fatty Acids
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: EPA (P205)
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: DHA (P226)
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: DPA (P225)
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Beans and Peas (Legumes)
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Whole Grains
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Cured Meats
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Poultry
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Nuts and Seeds
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Cheeses
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Self-reported Diet Components and Food Groups: Added Sugars
Time frame: Baseline (Burst 1) and 9 months (Burst 2)
Symbol Search Task Performance
Time frame: Baseline (Burst 1), and 9 months (Burst 2), 18 months (Burst 3), and 27 months (Burst 4) post-intervention
Grid Memory Task Performance
Time frame: Baseline (Burst 1), and 9 months (Burst 2), 18 months (Burst 3), and 27 months (Burst 4) post-intervention
Color Shapes Task Performance
Time frame: Baseline (Burst 1), and 9 months (Burst 2), 18 months (Burst 3), and 27 months (Burst 4) post-intervention
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Dec 2024.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Background: PubMed 36396064Mossavar-Rahmani Y, Shaw PA, Hakun JG, Katz MJ, Wylie-Rosett J, Sliwinski MJ. Multicultural Healthy Diet to Reduce Cognitive Decline & Alzheimer's Disease Risk: Study protocol for a pilot randomized controlled trial. Contemp Clin Trials. 2023 Jan;124:107006. doi: 10.1016/j.cct.2022.107006. Epub 2022 Nov 14.
- Derived from this study: PubMed 40412481Mossavar-Rahmani Y, Hyun N, Hakun JG, Katz MJ, Pavlovic JM, Zetterberg H, Wang Z, Yang JB, Wylie-Rosett J, Hebert JR, Sliwinski MJ, Shaw PA. The effects of the Multicultural Healthy Diet on cognitive decline and Alzheimer's disease risk: a phase II randomized controlled trial in middle-aged adults. Am J Clin Nutr. 2025 Jul;122(1):48-59. doi: 10.1016/j.ajcnut.2025.05.011. Epub 2025 May 22.
- Derived from this study: PubMed 39427230Hakun JG, Benson L, Qiu T, Elbich DB, Katz M, Shaw PA, Sliwinski MJ, Mossavar-Rahmani Y. Cognitive Health Benefits of Everyday Physical Activity in a Diverse Sample of Middle-Aged Adults. Ann Behav Med. 2025 Jan 4;59(1):kaae059. doi: 10.1093/abm/kaae059.
- Individual participant dataSharing planned: Yes. Data and specimens will be shared with potential collaborators, after obtaining participant consent, consistent with HIPPA guidelines
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Yasmin Mossavar-Rahmani, Ph.D, RD principal investigator
Albert Einstein College of Medicine
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Multicultural Healthy Diet and Usual Diet plus Self-Care in people with Diet Modification and Cognitive Decline, run by Albert Einstein College of Medicine at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 12 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Yes. Results are posted in the registry (first posted 12 Dec 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Mean Global Composite Cognition Score From Baseline (time frame: Baseline (Burst 1) and 9 months (Burst 2)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03240406, which also lists 3 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Dec 2024.