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A pilot study to determine the efficacy and feasibility of Herbal tea

A pilot study to determine the efficacy and feasibility of Herbal tea (HT001) for Prolonged Fatigue : a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0001966
Enrollment
40
Registered
2016-07-12
Start date
2015-12-28
Completion date
Unknown
Last updated
2019-05-20

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

Conditions

None listed

Interventions

Others : The test is manufactured by applying human herbal tea Therapy company after inspection at the Korea Institute of Oriental Medicine Human applicable tests conducted agencies. Herbal tea were p

Sponsors

Kyung Hee University Oriental Medicine Hospital at Gangdong
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Aged 35-45 ? chorinic fatigue ? Chalder Fatigue Scale over 15points ? Mibyung Scale over 14points ? careerman

Exclusion criteria

Exclusion criteria: ? primary sleep disorder (Sleep Apnea, Narcolepsy) ? depression over 5 years ? having a fatal history causing chronic fatigue ? having a mental illness causing chronic fatigue ? having a medicine history for example antihypertensive, antidepressants,narcotic,antihistaminic ? no fatigue in questionnarie test ? have treated within a month by medicine or oriental medicine ? pregnant women , nursing mothers and who are planning a pregnancy within 6 months ? night duty , shiftwork ? taking medication that may affect the clinical study or people who didn't follow clinical compliance ? recent characters participated in another clinical trial within 3 months

Design outcomes

Primary

MeasureTime frame
Revised Chalder Fatigue Scale

Secondary

MeasureTime frame
Pittsburgh Sleep Quality Index;EuroQol 5 Dimensions Questionnaire;SF-12 Health Survey;Beck Depression Inventory;Psychosocial Well-being Index Short Form;Vital sign;Skin Temperature;Grip Strength;Pulse Wave;Heart Rate Variability;Body Composition;Blood test;Physical somatype, facial & tongue image;Mibyung Questionnaire;Pattern/syndrom Identification Questionnaire;Adverse events

Countries

Korea, Republic of

Contacts

Public ContactMinwoo Hwang

Kyung Hee University

azure92@hanmail.net+82-2-440-7289

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026