Clinical trial Recruiting at 1 site Observational Ages 18 and up

Framework and dissemination plan for clinical guidelines about herb-drug interactions

Official title: Study Protocol for Developing a Methodological Framework and a Theory-informed Dissemination Plan for Herb-drug Interactions-related Clinical Practice Guidelines: a Delphi Survey and a Semi-structured Interview Study

Run by Chinese University of Hong Kong · NCT07248826 · Data updated 2026-11-12

This project will try to develop and share a practical framework using expert Delphi surveys and interviews to help clinicians and guideline developers manage herb–drug interactions.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment40 (estimated)
SponsorChinese University of Hong Kong
Academic / other
Locations1 site (Hong Kong, Hong Kong)
StatusRecruiting
StartedFebruary 1, 2026
Main results expectedFebruary 2027
Study endsAugust 2027
Registry record updatedOctober 21, 2026
Trial IDNCT07248826 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are registered Chinese medicine practitioners, herbalists, researchers in integrated Chinese–Western medicine, physicians working in integrated settings, and healthcare administrators or policymakers involved in guideline development.

Probably not a fit

Patients seeking direct clinical treatment or those who do not use herbal medicines are unlikely to receive direct personal benefit from this methodological project.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study uses a Delphi survey to build expert consensus on the key components of a methodological framework for herb–drug interaction clinical practice guidelines. Semi-structured interviews with practitioners, researchers, and policymakers will explore barriers and facilitators to guideline uptake. Findings will be used to create a theory-informed dissemination plan aimed at promoting guideline use locally and internationally. The work is coordinated from the Chinese University of Hong Kong and allows remote participation in multiple languages.

Why it matters

Potential benefit: If successful, this work could reduce harmful herb–drug interactions by producing clearer, evidence-based guidelines and a plan to get them used in clinical practice.

How similar studies have gone: Delphi consensus methods and theory-informed dissemination plans have successfully shaped guidelines in other clinical areas, but applying these approaches specifically to herb–drug interactions is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Registered Chinese medicine practitioners, herbalists, or researchers in the field of integrated Chinese and Western medicine;
* or physicians providing care in integrated Chinese and Western medicine settings;
* or healthcare administrators or policymakers from clinics/hospitals directly involved in developing or reviewing clinical practice guidelines related to integrated Chinese and Western medicine.

Exclusion Criteria:

* Panelists who are unable to commit to participating in all rounds of the Delphi process;
* or panelists who are unable to complete the online questionnaire in either Chinese or English;
* or panelists who are unable to conduct the interview in either English or Cantonese.

Where it's running

  • School of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong
    Hong Kong, Hong Kong, Hong Kong
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.