Pain SyndromeNCT06141902
The Effects of Jing Si Herbal Tea on Physical and Psychological Symptoms in Peripheral Blood Hematopoietic Stem Cell Donors
A study testing Jing Si Herbal Drink in people with Pain Syndrome and Emotional Stress, run by Buddhist Tzu Chi General Hospital at 1 site in Taiwan.
Trial summary
This study aim to explore the impact of Jing Si Herbal Tea on pain and emotional stress in peripheral blood stem cell donors. Read more about this study
- Who is it for?
- Ages 20 to 55 yearsHealthy volunteers can take part
- Conditions the study is for
- Pain Syndrome, Emotional Stress
- What is being tested?
- Jing Si Herbal Drink
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteTaiwan
- Study dates
- 18 Sep 2025to 31 Dec 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 55 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- health Men or women aged 20 to 55 years old
- willing to take Jing Si Herbal Drink
Who cannot join
- no willing to take Jing Si Herbal Drink;
- Previously already take Jing Si Herbal Drink daily
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Taiwan1 site
Hualiien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
Hualien City, 970
About this study
This study aim to explore the impact of Jing Si Herbal Tea on pain and emotional stress in peripheral blood stem cell donors.
- Conditions
- Pain Syndrome, Emotional Stress
- Being tested
- Jing Si Herbal Drink
- Medical subject headings
- Somatoform Disorders, Stress, Psychological
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Jing Si Herbal DrinkOther
Jing Si Herbal Drink
| Study group | Role | What they receive |
|---|---|---|
| NORMAL | Other | daily diet Receives: Other: Jing Si Herbal Drink |
| Take Jing Si Herbal Drink | No intervention | Take Jing Si Herbal Drink daily |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in pain assessed by questionnaires
For each of the pain sites includes: headache、bone、joint \& muscle, indicate the severity of present using the following scale (baseline vs. follow-up).
grade 0: fully active, able to carry on all pre-disease performance without restriction
grade 1: restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature, e.g. light housework, office work
grade 2: ambulatory and capable of all self-care but unable to carry out any work activities, up and about more than 50% of waking hours
grade 3: capable of only limited self-care, confined to bed or chair more than 50% of waking hours
grade 4: completely disabled, cannot carry on any self-care, totally confined to bed or chair
grade 5: dead
Measured: 5 day
Secondary outcomes (1)
Changes in anxiety assessed by questionnaires
Difference in donor Health State Trait Anxiety Index (STAI) scores (baseline vs. follow-up).
The STAI questionnaire consists of 20 items for assessing "state anxiety" and 20 items for assessing "trait anxiety," with a raw score of 20 to 60 points for each scale.
The state anxiety scale evaluates the current state of anxiety associated with a special situation, measuring subjective feelings of apprehension, tension, nervousness, worry, and activation of the autonomic nervous system, whereas the trait anxiety scale evaluates proneness to anxiety .
The level of anxiety was determined according to the percentile rank obtained using the raw score of each questionnaire and was classified as low anxiety (1st-23th percentile), moderate anxiety (25th75th percentile) and high anxiety (77th-99th percentile).
Measured: 21 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Nov 2023
- Study start18 Sep 2025 (estimated)
- Primary completion31 Dec 2027 (estimated)
- Study completion31 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pain SyndromeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Buddhist Tzu Chi General Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06141902
- Sponsor's protocol ID
- IRB111-125-A
- Other IDs
- IMAR-111-01-17
- Status last verified
- Oct 2024
- First submitted
- 5 Nov 2023
- Last updated
- 19 Sep 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effects of Jing Si Herbal Tea on Physical and Psychological Symptoms in Peripheral Blood Hematopoietic Stem Cell Donors
- ClinicalTrials.gov ID
- NCT06141902
- Acronym / sponsor ID
- IRB111-125-A
- Conditions
- Pain Syndrome, Emotional Stress
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Buddhist Tzu Chi General HospitalUniversity, hospital or other
- Study start
- 18 Sep 2025 (estimated)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 31 Dec 2027 (estimated)
- First posted
- 21 Nov 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aim to explore the impact of Jing Si Herbal Tea on pain and emotional stress in peripheral blood stem cell donors.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| NORMAL | Other | Other: Jing Si Herbal Drinkdaily diet |
| Take Jing Si Herbal Drink | No intervention | –Take Jing Si Herbal Drink daily |
Who may qualify
- Ages
- 20 to 55 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- health Men or women aged 20 to 55 years old
- willing to take Jing Si Herbal Drink
Key exclusion criteria (2 listed)
- no willing to take Jing Si Herbal Drink;
- Previously already take Jing Si Herbal Drink daily
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Jing Si Herbal DrinkJing Si Herbal Drink | Other | NORMAL |
Primary outcome
Changes in pain assessed by questionnaires
Time frame: 5 day
For each of the pain sites includes: headache、bone、joint \& muscle, indicate the severity of present using the following scale (baseline vs. follow-up). grade 0: fully active, able to carry on all pre-disease performance without restriction grade 1: restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature, e.g. light housework, office work grade 2: ambulatory and capable of all self-care but unable to carry out any work activities, up and about more than 50% of waking hours grade 3: capable of only limited self-care, confined to bed or chair more than 50% of waking hours grade 4: completely disabled, cannot carry on any self-care, totally confined to bed or chair grade 5: dead
1 secondary outcome
Changes in anxiety assessed by questionnaires
Time frame: 21 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Sep 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Jing Si Herbal Drink in people with Pain Syndrome and Emotional Stress, run by Buddhist Tzu Chi General Hospital at 1 site in Taiwan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 19 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in pain assessed by questionnaires (time frame: 5 day). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Sep 2025.