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Effects of Jing Si Herbal Tea on Quality of Life and Sleep in Dementia and Their Caregivers

Effects of Jing Si Herbal Tea on Quality of Life and Sleep Among Patients With Dementia and Their Caregivers: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06198699
Enrollment
400
Registered
2024-01-10
Start date
2025-01-17
Completion date
2026-12-01
Last updated
2026-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caregiver Burden, Dementia, Quality of Life

Keywords

dementia, caregiver, quality of life, Jing Si Herbal Tea, psychosocial health, randomized controlled trial

Brief summary

Jing Si Herbal Tea has been found to be effective in improving health for the conditions of cancers, aging, depression, and sleep. Such evidence has been shown in animal models and clinical research with publications in the international journals. However, empirical evidence regarding the effectiveness of Jing Si Herbal Tea for patients with dementia and their caregivers on their quality of life and psychosocial health remains unclear. Therefore, the present project aims to investigate the feasibility of taking Jing Si Herbal Tea among patients with dementia; then, to investigate if Jing Si Herbal Tea could improve quality of life and psychosocial health for patients with dementia and their caregivers. The project will be three years. The first year will examine the feasibility for the patients with dementia. A total of 100 patients with dementia will be recruited and they will be informed to take the Jing Si Herbal Tea two times per day (one time in the morning and another time in the afternoon). All the participants will be measured for their quality of life and psychosocial health at baseline, three months after baseline, and six months after baseline, to have initial evidence of the improvements in quality of life and psychosocial health without having a control group. The second year will recruit 200 patients with dementia and randomly assign them into a treatment group (taking Jing Si Herbal Tea) and a control group (taking placebo). All the participants will be measured for their quality of life and psychosocial health at baseline, three months after baseline, and six months after baseline, to investigate the strong evidence of Jing Si Herbal Tea on quality of life and psychosocial health. The third year will recruit 200 caregivers of patient with dementia and randomly assign them into a treatment group (taking Jing Si Herbal Tea) and a control group (taking placebo). All the participants will be measured for their quality of life and psychosocial health at baseline, three months after baseline, and six months after baseline, to investigate the strong evidence of Jing Si Herbal Tea on quality of life and psychosocial health.

Interventions

DIETARY_SUPPLEMENTJing Si Herbal Tea

Consuming Jing Si Herbal Tea for three months; twice per day with each time 14 g of Jing Si Herbal in 600 ml water

Sponsors

National Cheng Kung University
Lead SponsorOTHER
Buddhist Tzu Chi General Hospital
CollaboratorOTHER
Tzu Chi University
CollaboratorOTHER
E-DA Hospital
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

For people with dementia: Inclusion Criteria: * diagnosis of dementia * 50 years or older * with sufficient cognition to complete the questionnaires * can communicate using Mandarin or Taiwanese

Exclusion criteria

* with renal function problems * not suitable for Jing Si Herbal Tea after evaluation from a psychiatrist/physician * with the condition of change the commencement of guardianship (or commencement of assistance) For caregivers: Inclusion Criteria: * caregivers of people with dementia for more than half years * 20 years or older * with sufficient cognition to complete the questionnaires * can communicate using Mandarin or Taiwanese

Design outcomes

Primary

MeasureTime frameDescription
World Health Organization Quality of Life Assessment for age (WHOQOL-AGE) [for people with dementia]baseline; 3 months after baseline; 6 months after baselinequality of life measure; score range 13-65; higher score indicates better quality of life
Insomnia Severity Index [for both people with dementia and their caregivers]baseline; 3 months after baseline; 6 months after baselinesleep problem measure; score range 0-28; higher score indicates more severe insomnia
World Health Organization Quality of Life Assessment brief version (WHOQOL-BREF) [for caregivers]baseline; 3 months after baseline; 6 months after baselinequality of life measure; score range 4-20; higher score indicates better quality of life

Secondary

MeasureTime frameDescription
Katz Index of Independence in Activities of Daily Living [for people with dementia]baseline; 3 months after baseline; 6 months after baselineactivities of daily living function measure; score range 0-6; higher score indicates better activities of daily living
5 items of Geriatric Depression Scale [for people with dementia and their caregivers]baseline; 3 months after baseline; 6 months after baselinedepression measure; score range 0-5; higher score indicates greater depression
Short Portable Mental Status Questionnaire [for people with dementia]baseline; 3 months after baseline; 6 months after baselinecognition measure; score range 0-10; higher score indicates poor cognition
Clinical Frailty Scale [for people with dementia]baseline; 3 months after baseline; 6 months after baselinefrailty measure; score range 1-9; higher score indicates more frail
Integrated care for older people [for people with dementia]baseline; 3 months after baseline; 6 months after baselineintrinsic capacity measure; score range 0-13; higher score indicates poorer intrinsic capacity
Attitude and Thoughts Toward Older People Scale [for people with dementia and their caregivers]baseline; 3 months after baseline; 6 months after baselineageism measure; score range 17-85; higher score indicates higher level of ageism
Depression, Anxiety, Stress Scale-21 [for people with dementia and their caregivers]baseline; 3 months after baseline; 6 months after baselinepsychological distress measure; score range 0-63; higher score indicates greater distress
12 item of Zarit Burden Interview [for caregivers]baseline; 3 months after baseline; 6 months after baselinecaregiver burden measure; score range 0-48; higher score indicates greater burden

Countries

Taiwan

Contacts

CONTACTChung-Ying Lin, PhD
cylin36933@gs.ncku.edu.tw+886-2353535
PRINCIPAL_INVESTIGATORHao-Ming Li, MD

Buddhist Tzu Chi General Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026