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PlainTrials
RecruitingNot a traditional drug phaseinterventionalRules rewrite

Not a traditional drug phase: testing Chinese herbal medicine for Acupuncture

This study aims to measure the how well it works of acupuncture as a treatment for Attention Deficit Hyperactivity Disorder (ADHD) in children aged 6-12 years. Using a mixed-methods approach, the research will triangulate data from acupoint data mining, treatment outcomes assessment, and patient perspectives to provide a comprehensive analysis of acupuncture's potential therapeutic benefits for ADHD.

Official registry: https://clinicaltrials.gov/study/NCT06860763 · The Third Affiliated Hospital of Beijing University of Chinese Medicine · enrollment listed as 120

What this phase means

This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

If you join, the listed intervention(s) are Chinese herbal medicine, or Acupuncture. The registry lists allocation as randomized. This study aims to measure the how well it works of acupuncture as a treatment for Attention Deficit Hyperactivity Disorder (ADHD) in children aged 6-12 years.

They plan to enroll about 120 people at Beijing. Taking part typically means taking a study drug (or dummy pill), using or being fitted with a device plus check-ins.

Official title (unrewritten)

Clinical Study on Acupuncture Treatment for Attention Deficit Hyperactivity Disorder.

Interventions: Chinese herbal medicine, Acupuncture

Primary outcome (registry wording): SNAP-IV

Who it is for (from inclusion criteria)

  • Ages 6 Years to 12 Years
  • Patients will be considered for enrolment if they meet the criteria of:
  • A confirmed diagnosis of ADHD based on the DSM-5 criteria for ADHD (Western medical diagnosis) and in accordance with the ADHD Chinese Medicine Clinical Trial Design and Evaluation Technical Guidelines
  • Aged between 6 and 12 years
  • No use of any other pharmacological treatments (both Western and traditional Chinese medicine) within the two weeks prior to the start of the study
  • An IQ score of greater than 80, as determined by the Raven's Progressive Matrices test
  • The participant has not participated in any other clinical trials

Public study contact (from the registry)

Tananan Sangwanit, Ph.D.student

+8615201052193

tananan.sangwanit@gmail.com

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

1 listed

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FAQ about this NCT record

Is NCT06860763 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT06860763?

Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT06860763?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

How to read a ClinicalTrials.gov record · Questions to ask the coordinator · Glossary