- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05342896
Effect of Mediterranean-DASH Intervention for Neurodegenerative Delay Plus Forest Bathing (MINDdiet)
Effect of Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) Plus Forest Bathing (FB) on Blood Pressure and Cognitive Health for Those Who Are Aged 50 and Above With Hypertension
This proposed study will be the first to investigate the effect of the Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) Plus Forest Bathing (FB) on blood pressure (BP) and cognitive health for those who are aged 50 and above with hypertension. Hypertension is a major public health issue, and four developments make this research study remarkably important.
It is well-documented the Mediterranean diet and Dietary Approach to Stop Hypertension (DASH) diet have demonstrated efficacy for improving cardiovascular and cognitive health. The Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) diet is a hybrid of the Mediterranean and DASH diets. FB promotes relaxation by inducing the activity of the parasympathetic nervous system, which decrease Heart rate and BP. The initial quantitative phase of the study, a three-arm RCT will be conducted to examine the effects of MIND, MIND plus FB and usual care as control on hypertension. The subsequent qualitative phase in-depth focus group interview is to explore the barriers and facilitators of MIND diet uptake and FB. The participants will include older HK Chinese adults who meet the criteria for hypertension stage 1 and stage 2 of the AHA. The primary outcomes are systolic BP and the secondary outcomes are point of care test of lipid panel, cognitive function, waist-to-hip ratio, body fat percentages and body mass index. The outcome measurements will be recorded before the interventions (T0), immediately after the 4-week face-to-face intervention (T1) and 12-week after 3-month intervention (T2). A total of 48 those who are aged 50 and above with hypertension will be recruited from community centres in Hong Kong to Randomized Controlled Trial and 10 participants differing in levels of compliance to MIND and FB will be purposively selected for face-to-face semi-structured focus group interviews.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Research aim
- This study will aim to investigate the effect of MIND and MIND plus FB on hypertension.
- To examine the effect of MIND alone on hypertension by controlling other covariates.
- To describe the perceived capability, opportunity, and motivation to the uptake of the MIND and FB.
- To explore the barriers and facilitators to the MIND and FB.
The MIND-FB is proposed in response to (i) high BP is the one of important risk factors for chronic diseases. (ii) although there is robust evidence to show that the important of lowering BP to reduce chance of getting cardiovascular morbidity and mortality, the global burden of hypertension is still increasing. The objectives of MIND-FB are to perform high quality research focused on those who are aged 50 and above, novel transdisciplinary approaches to ensure the building capacity of public health workforce to deliver quality lifestyle modification intervention to control BP of those who are aged 50 and above.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Queenie Law, PhD
- Phone Number: 39702974
- Email: qlaw@hkmu.edu.hk
Study Locations
-
-
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Hong Kong, Hong Kong
- Dr. Queenie Law
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- aged 60 and above;
- Chinese ethnicity;
- ability to speak and understand Chinese;
- fulfilment of the AHA criteria for stage 1 and stage 2 hypertension; and
- who could walk independently
Exclusion Criteria:
- have allergy to more than one type of food (nuts, berries, olive oil, or fish);
- participation in any dietary or relaxation programme within the past 3 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: MIND diet intervention
3-month intervention of dietary counseling to adhere to the MIND diet
|
MIND diet intervention will be a 3-month nutrition programme consisting of 4 face-to-face nutrition counselling sessions (one session per week, 60 min per session) in the activity room of each participating community centre.
All intervention sessions will be conducted by a registered nutritionist and trained student helpers.
In the nutrition sessions, the participants will learn to modify their diet to meet MIND diet guidelines.
|
Experimental: MIND-plus-FB intervention
3-month intervention of dietary counseling to adhere to the MIND diet plus Forest Bathing intervention
|
MIND diet intervention will be a 3-month nutrition programme consisting of 4 face-to-face nutrition counselling sessions (one session per week, 60 min per session) in the activity room of each participating community centre.
All intervention sessions will be conducted by a registered nutritionist and trained student helpers.
In the nutrition sessions, the participants will learn to modify their diet to meet MIND diet guidelines.
Forest Bathing will be another session per week, 2 hours forest bathing sessions on 4-consecutive weekends in a country park at daytime with sunny, cloudy or drizzling conditions.
The walking distance for each forest bathing is one to two kilometres.
The coach-to-participant ratio is approximately 1:16.
Participants will then be required to self-practice 2h FB in the country park at daytime at the weekends of 8th week and 12th week of the intervention.
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No Intervention: Control group
For the control group, the participants will be received routine care.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Blood pressure
Time Frame: Three months
|
By systolic blood pressure, measured by a digital automatic device
|
Three months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in lipid panel of HDL cholesterol, triglycerides and LDL cholesterol
Time Frame: Three months
|
By point of care test (POCT) of lipid panel (HDL-cholesterol, triglycerides and LDL-cholesterol)
|
Three months
|
Change in body fat percentages
Time Frame: Three months
|
By body fat percentages, measured by bioelectrical impedance analysis
|
Three months
|
Change in cognitive function
Time Frame: Three months
|
By cognitive function, measured by Hong Kong version of the Montreal Cognitive Assessment, cut-off score of 21/22 after adjustment of education level is recommended as indication for further evaluation of cognitive impairment and dementia.
Lower scores mean worse outcome.
The minimum score is 0 and maximum score is 30.
|
Three months
|
Change in waist circumference
Time Frame: Three months
|
By waist circumference, measured by tape meter between the lower rib and iliac crest
|
Three months
|
Change in diet scores
Time Frame: Three months
|
By diet scores, measured by total scores using predefined criteria of MIND diet.
A value of 0.0, 0.5, or 1.0 is assigned to each food group.
For high intake of brain healthy food group, participants will receive a score of 1 and the score is reversed for unhealthy food group.
The total MIND diet score will be computed by summing all food groups eaten, with a maximum score of 15 representing the highest adherence to the MIND diet.
|
Three months
|
Collaborators and Investigators
Publications and helpful links
General Publications
- 1. Morris M C., Tangney CC, Wang Y, Sacks FM, Barnes LL, Bennett, DA, & Aggarwal N T. MIND diet slows cognitive decline with aging. Alzheimer's and Dementia. 2015. 11(9): 1015-1022. 2. Morris MC, Tangney CC, Wang Y, Sacks FM, Bennett DA, & Aggarwal NT. MIND diet associated with reduced incidence of Alzheimer's disease. Alzheimer's and Dementia. 2015. 11(9): 1007-1014. 3. Aminianfar A, Hassanzadeh Keshteli A, Esmaillzadeh A, & Adibi P. Association between adherence to MIND diet and general and abdominal obesity: A cross-sectional study. Nutrition Journal. 2020. 19(1): 1-9. 4. Arjmand G, Abbas-Zadeh M, & Eftekhari MH. Effect of MIND diet intervention on cognitive performance and brain structure in healthy obese women: A randomized controlled trial. In bioRxiv. bioRxiv. 2020.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HE-NHS2021/02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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