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Effect of Mediterranean-DASH Intervention for Neurodegenerative Delay Plus Forest Bathing

Not Applicable
Completed
Conditions
High Blood Pressure
Interventions
Behavioral: MIND diet
Behavioral: Mind diet plus Forest Bathing
Registration Number
NCT05342896
Lead Sponsor
Hong Kong Metropolitan University
Brief Summary

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.

Detailed Description

Research aim

1. This study will aim to investigate the effect of MIND and MIND plus FB on hypertension.

2. To examine the effect of MIND alone on hypertension by controlling other covariates.

3. To describe the perceived capability, opportunity, and motivation to the uptake of the MIND and FB.

4. 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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
48
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 & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
MIND diet interventionMIND diet3-month intervention of dietary counseling to adhere to the MIND diet
MIND-plus-FB interventionMind diet plus Forest Bathing3-month intervention of dietary counseling to adhere to the MIND diet plus Forest Bathing intervention
Primary Outcome Measures
NameTimeMethod
Change in Blood pressureThree months

By systolic blood pressure, measured by a digital automatic device

Secondary Outcome Measures
NameTimeMethod
Change in lipid panel of HDL cholesterol, triglycerides and LDL cholesterolThree months

By point of care test (POCT) of lipid panel (HDL-cholesterol, triglycerides and LDL-cholesterol)

Change in body fat percentagesThree months

By body fat percentages, measured by bioelectrical impedance analysis

Change in cognitive functionThree 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.

Change in waist circumferenceThree months

By waist circumference, measured by tape meter between the lower rib and iliac crest

Change in diet scoresThree 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.

Trial Locations

Locations (1)

Dr. Queenie Law

🇭🇰

Hong Kong, Hong Kong

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