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NCT05342896: MINDdiet
Effect of Mediterranean-DASH Intervention for Neurodegenerative Delay Plus Forest Bathing
NA trial testing MIND diet in High Blood Pressure in 48 participants. Completed in 31 March 2023.
30 July 2022
Quick facts
| Lead sponsor | Hong Kong Metropolitan University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | health services research |
| Enrollment | 48 |
| Start date | 3 January 2021 |
| Primary completion | 30 July 2022 |
| Estimated completion | 31 March 2023 |
| Sites | 1 location across Hong Kong |
Drugs / interventions tested
- MIND diet
- Mind diet plus Forest Bathing
Conditions studied
- High Blood Pressure — all drugs for High Blood Pressure →
Sponsor
Hong Kong Metropolitan University
Who can join
60 and older, any sex, with High Blood Pressure. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Effects of the Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) diet and forest bathing in improving cognitive and metabolic health among hypertensive older adults: a feasibility randomised controlled trial.
Law QPS, Yau KKY, Tyrovolas S, Kwan RYC. · · 2026 · PMID 41514353 · DOI 10.1186/s40795-026-01240-4
Verify or expand the search:
- PubMed search for NCT05342896
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Related trials
Other trials of MIND diet
Trials testing the same drug.
- NCT06351423 — The Effectiveness of MIND Diet and Forest Bathing on Stress Reduction · NA · unknown
- NCT05982860 — The Effects of the MIND Diet on Oxidative Stress, Inflammation and Neurodegenerative Risk Biomarkers · NA · completed
- NCT04654936 — Effectiveness of a 12 Week Theory Driven Intervention Promoting Adherence to the MIND Diet · NA · completed
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Currently open trials in the same condition.
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Other Hong Kong Metropolitan University trials
Trials by the same sponsor.
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- NCT07503535 — Mindful Simulation Training in Palliative Care Education for Nursing Students · NA · active not recruiting
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05342896 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hong Kong Metropolitan University
- Last refreshed: 3 November 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05342896.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing