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Status unknownNCT05801575Updated Apr 6, 2023

CHM Teabag Decrease Stroke Risk Among Hong Kong Elderly

An interventional study of Chinese Herbal Medicine (CHM) teabag in Stroke, Risk Reduction and Elderly, sponsored by Hong Kong Baptist University. Status unknown at 1 site in China. Open to participants aged 54 Years to 84 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-04-06.

Sponsored by Hong Kong Baptist University · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Mar 2023), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
912
Allocation
Randomized
Ages
54 Years to 84 Years
Sex
All
01

Study summary

This stepped wedge cluster randomized controlled trial aims to examine the efficacy and safety of CHM teabag in decreasing stroke risk by machine-learning-based retinal image analysis in elderly population.

Read the detailed description

This is a stepped wedge cluster randomized controlled trial design. This study aims to examine the efficacy and safety of CHM teabag in decreasing stroke risk by machine-learning-based retinal image analysis in elderly population.

A total of 912 participants will be recruited from 9 clinics. 2\~3 clinics will represent a cluster unit. The stepped wedge design will consist of four groups each containing four randomly allocated cluster units, allocated to either 4, 8, 12, or 16 weeks of the intervention. The intervention is Chinese herbal teabag treatment, which will consist of five Chinese herbs (a total of 10g). The first group will receive 16 weeks of the intervention, the second group will receive 12 weeks, the third group will receive 8 weeks, and the forth group will receive 4 weeks.

The primary outcome measure is the stroke risk estimated with Automatic Retinal Image Analysis (ARIA). Secondary outcome measures include Framingham Stroke Risk Score (FSRS), cognitive impairment risk estimated with ARIA, Hong Kong version of the Montreal Cognitive Assessment (MoCA), Constitution in Chinese Medicine Questionnaire (CCMQ), World Health Organization Quality-of-Life Scale (WHOQOL-BREF), Health-promoting lifestyle profile II (HPLP-II), and adverse events.

02

Conditions studied

  • Stroke
  • Risk Reduction
  • Elderly

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Keywords

  • Stroke
  • Risk Reduction
  • Chinese Herbal Medicine
  • Automatic Retinal Image Analysis
  • Teabag
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,013 are open to participants now.

This study's planned enrollment of 912 is above the median of 50 across 5,366 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Hong Kong Baptist University is the lead sponsor of 79 studies on the registry; 22 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
54 Years to 84 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age between 54-84y.
  • With phlegm dampness constitution and blood stasis constitution on the TCM constitution test table.
  • Stable vital signs without previous history of stroke.
  • Sufficient sensorimotor and language competency for completing assessments.

Exclusion criteria

Exclusion Criteria:

  • Allergic history to Chinese herbal drugs or a known allergy to the ingredients of the teabag.
  • Taking any anticoagulants, such as warfarin.
  • With unconsciousness, aphasia, and cognitive dysfunction.
  • With a past history of brain diseases (e.g., mental illness, consciousness disorder due to head trauma, previous brain surgery, or spastic disease).
  • With severe heart, liver, or kidney disease or bleeding disorders.
  • With other serious diseases.
  • Cataracts or other eye diseases that affected retinal image taking.
  • Distressed with a flashlight or have experience with photosensitive seizures.
  • Pregnancy or lactation female.
  • Any physical examination findings, or history of any illness, or concomitant medications that, in the opinion of the study investigator, might not be suitable to participate in the study.
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
912 participants (estimated)

Study arms

  • Experimental
    Chinese Herbal Medicine (CHM) teabag, Cluster 1

    Intervention Cluster 1 is the first intervention arm designed to examine the efficacy and safety of CHM teabag in decreasing stroke risk by machine-learning-based retinal image analysis in elderly population. It will receive 16 weeks of the intervention.

    Drug: Chinese Herbal Medicine (CHM) teabag

  • Experimental
    CHM teabag, Cluster 2

    Intervention Cluster 2 is the second intervention arm designed to examine the efficacy and safety of CHM teabag in decreasing stroke risk by machine-learning-based retinal image analysis in elderly population. It will receive 12 weeks of the intervention.

    Drug: Chinese Herbal Medicine (CHM) teabag

  • Experimental
    CHM teabag, Cluster 3

    Intervention Cluster 3 is the third intervention arm designed to examine the efficacy and safety of CHM teabag in decreasing stroke risk by machine-learning-based retinal image analysis in elderly population. It will receive 8 weeks of the intervention.

    Drug: Chinese Herbal Medicine (CHM) teabag

  • Experimental
    CHM teabag, Cluster 4

    Intervention Cluster 4 is the fourth intervention arm designed to examine the efficacy and safety of CHM teabag in decreasing stroke risk by machine-learning-based retinal image analysis in elderly population. It will receive 4 weeks of the intervention.

    Drug: Chinese Herbal Medicine (CHM) teabag

Interventions

  • DrugChinese Herbal Medicine (CHM) teabag

    Each teabag contains five herbs: Radix et Rhizoma (三七, Sanqi), Moutan Cortex (牡丹皮, Mudanpi), Puerariae Lobatae Radix (葛根, Gegen), Rosae Rugosae Flos (玫瑰花, Meiguihua), and Citri Grandis Exocarpium (化橘紅, Huajuhong). These herbs are benefit to promoting blood circulation, dredging meridians and collaterals, strengthening spleen, regulating qi and decreasing phlegm in Chinese Medicine theories.

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What researchers measure

Primary outcomes

  1. Automatic Retinal Image Analysis (ARIA).

    The primary outcome will be the score change of stroke risk estimated with Automatic Retinal Image Analysis (ARIA). The ARIA stroke risk score is represented by a probability score which is from 0 to 1. Low risk score is less than 0.5. Moderate score is 0.5 - 0.7. High risk score is more than 0.7.

    Time frame: 16 weeks

Secondary outcomes

  1. Framingham Stroke Risk Score (FSRS)

    The Framingham Stroke Risk Score (FSRS) combines stroke risk factors to predict 10-year probability of stroke. Factors included in the FSRS are age, sex, systolic blood pressure, use of antihypertensive medications, diabetes, smoking, atrial fibrillation, left ventricular hypertrophy and prevalent coronary heart disease. Higher score is associated with higher stroke risk.

    Time frame: 16 weeks

  2. Cognitive impairment risk

    The severity of WMH changes can be estimated by taking the fundus retinal image and put to the ARIA algorithm, increasing score means increasing severity.

    Time frame: 16 weeks

  3. Montreal Cognitive Assessment (MoCA)

    The Montreal Cognitive Assessment (MoCA) was designed as a rapid screening instrument for mild cognitive dysfunction. Scoring of HK MoCA ranges from 0 to 30 points. A score of 26 or above is considered normal.

    Time frame: 16 weeks

  4. Constitution in Chinese Medicine Questionnaire (CCMQ)

    The CCMQ is applied to evaluate body constitution of each patient by score (Balanced Constitution, Qi-deficient Constitution, Yang-deficient Constitution, Yin-deficient Constitution, Phlegm-dampness Constitution, Damp-heat Constitution, Stagnant Blood Constitution, Stagnant Qi Constitution, and Inherited Special Constitution). Each constitution scale contains 6 to 8 items, with 1-5 numerical rating scale. The transformed score of each constitution scale is calculated.

    Time frame: 16 weeks

  5. World Health Organization Quality-of-Life Scale (WHOQOL-BREF)

    The WHOQOL-BREF is to measure the quality of life. The WHOQOL-BREF is a self-administered questionnaire comprising 26 questions on the individual's perceptions of their health and well-being over the previous two weeks. Each item is rated on a 5-point (1-5) scale. Higher scores denote higher quality of life.

    Time frame: 16 weeks

  6. Health-promoting lifestyle profile II (HPLP-II)

    The Health-Promoting Lifestyle Profile II continues to measure health promoting behavior, conceptualized as a multidimensional pattern of self-initiated actions and perceptions that serve to maintain or enhance the level of wellness, self-actualization and fulfillment of the individual. The total score of the HPLP II ranges from 52 to 208 and is measured by the mean score of the responses to all 52 HPLP items. The total HPLP II score is further classified into four levels: poor for the range 52-90, moderate for the range 91-129, good for the range 130-168, and excellent for the range 169-208. High scores in every subscale mean more frequent health-promoting behaviors.

    Time frame: 16 weeks

  7. Adverse events

    All adverse events (AEs) will be recorded.

    Time frame: 16 weeks

07

Study locations

1 of 1 sites recruiting
  • Hong Kong Baptist University Mr. & Mrs. Chan Hon Yin Chinese Medicine Specialty Clinic and Good Clinical Practice Centre
    Hong Kong, China
    • Zhao-xiang Bian, PhD · Contact · bzxiang@hkbu.edu.hk · (852) 3411 2905
    • Jialing Zhang, Mphil, BCM · Contact · zhangjialing@hkbu.edu.hk · (852) 3411 5024
    • Zhao-xiang Bian, PhD · Principal investigator
    • Chun Hoi CHEUNG · Sub investigator
    Recruiting
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References and documents

Publications

  • Murray CJ, Lopez AD. Mortality by cause for eight regions of the world: Global Burden of Disease Study. Lancet. 1997 May 3;349(9061):1269-76. doi: 10.1016/S0140-6736(96)07493-4. PubMed 9142060 ↗
  • Liu L, Wang D, Wong KS, Wang Y. Stroke and stroke care in China: huge burden, significant workload, and a national priority. Stroke. 2011 Dec;42(12):3651-4. doi: 10.1161/STROKEAHA.111.635755. Epub 2011 Nov 3. PubMed 22052510 ↗
  • Boehme AK, Esenwa C, Elkind MS. Stroke Risk Factors, Genetics, and Prevention. Circ Res. 2017 Feb 3;120(3):472-495. doi: 10.1161/CIRCRESAHA.116.308398. PubMed 28154098 ↗
  • ALPERS BJ, FORSTER FM, HERBUT PA. Retinal, cerebral and systemic arteriosclerosis; a histopathologic study. Arch Neurol Psychiatry. 1948 Nov;60(5):440-56. doi: 10.1001/archneurpsyc.1948.02310050017002. No abstract available. PubMed 18117474 ↗
  • Goto I, Katsuki S, Ikui H, Kimoto K, Mimatsu T. Pathological studies on the intracerebral and retinal arteries in cerebrovascular and noncerebrovascular diseases. Stroke. 1975 May-Jun;6(3):263-9. doi: 10.1161/01.str.6.3.263. PubMed 50653 ↗
  • Cheung CY, Ikram MK, Chen C, Wong TY. Imaging retina to study dementia and stroke. Prog Retin Eye Res. 2017 Mar;57:89-107. doi: 10.1016/j.preteyeres.2017.01.001. Epub 2017 Jan 3. PubMed 28057562 ↗
  • Guo VY, Cao B, Wu X, Lee JJW, Zee BC. Prospective Association between Diabetic Retinopathy and Cardiovascular Disease-A Systematic Review and Meta-analysis of Cohort Studies. J Stroke Cerebrovasc Dis. 2016 Jul;25(7):1688-1695. doi: 10.1016/j.jstrokecerebrovasdis.2016.03.009. Epub 2016 Apr 8. PubMed 27068777 ↗
  • Guo VY, Chan JC, Chung H, Ozaki R, So W, Luk A, Lam A, Lee J, Zee BC. Retinal Information is Independently Associated with Cardiovascular Disease in Patients with Type 2 diabetes. Sci Rep. 2016 Jan 12;6:19053. doi: 10.1038/srep19053. PubMed 26754623 ↗
  • Qu Y, Lee JJ, Zhuo Y, Liu S, Thomas RL, Owens DR, Zee BC. Risk Assessment of CHD Using Retinal Images with Machine Learning Approaches for People with Cardiometabolic Disorders. J Clin Med. 2022 May 10;11(10):2687. doi: 10.3390/jcm11102687. PubMed 35628812 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05801575
Lead sponsor
Hong Kong Baptist University
Responsible party
ZhaoXiang Bian (Professor, Hong Kong Baptist University) — Principal investigator
First posted
Apr 6, 2023
Start date
Feb 2, 2023
Primary completion
Aug 30, 2023 (estimated)
Completion
Oct 31, 2023 (estimated)
Last update
Apr 6, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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