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Qihuang needle therapy protocol for Parkinson's disease in 69 patients

Qihuang needle therapy protocol for Parkinson's disease in 69 patients
Photo by Dmytro Vynohradov / Unsplash
Key Takeaway
Consider this a protocol only; await trial results for efficacy and safety data.

This study is a randomized controlled trial protocol involving 69 patients with Parkinson's disease. It compares Qihuang needle therapy (QNT) to three groups: verum acupuncture, sham acupuncture, and wait-list control, with an 8-week follow-up period. The primary outcomes focus on efficacy and neurological effects, measured by UPDRS-III, NMSS, PDQ-39, muscle rigidity, and gait/balance parameters. Secondary outcomes include neuroimaging measures such as gray matter volume, functional connectivity, white matter integrity, nigral iron deposition, and neuromelanin content.

Safety and tolerability data are not reported in this protocol, as it is a pre-trial design document. Adverse events, serious adverse events, discontinuations, and tolerability details will need to be assessed in future results from the completed trial.

Key limitations include that this is only a protocol, so no results or efficacy data are available yet. The study phase, setting, and funding or conflicts of interest are not reported. Practice relevance is framed as potentially providing high-level mechanistic evidence for integrating QNT into Parkinson's disease care and optimizing integrative treatment strategies, but this depends on future trial outcomes. Clinicians should await published results before considering any changes to practice.

Study Details

Study typeRct
EvidenceLevel 2
PublishedApr 2026
View Original Abstract ↓
BackgroundParkinson's disease (PD) is a progressive neurodegenerative disorder for which no curative therapy currently exists. Qihuang needle therapy (QNT) is a novel acupuncture technique that has demonstrated clinical promise in alleviating PD symptoms, but its neuroplasticity mechanisms remain unexplored. This trial aims to investigate the efficacy and neurological effects of the QNT via multimodal MRI.MethodsThis triple-arm randomized controlled trial will enroll 69 PD patients randomized into three groups (1:1:1): verum acupuncture, sham acupuncture, or wait-list control. Patients in the verum and sham groups will receive eight treatment sessions over 4 weeks, followed by an 8-week follow-up period. The control group will not receive any acupuncture treatment throughout the trial. Clinical outcomes included the Unified Parkinson's Disease Rating Scale Part III (UPDRS-III), Non-Motor Symptoms Scale (NMSS), 39-item Parkinson's Disease Questionnaire (PDQ-39), muscle rigidity (shear-wave elastography), and gait/balance parameters (Footscan system). Multimodal MRI will evaluate neuroplasticity markers: gray matter volume, functional connectivity, white matter integrity, nigral iron deposition, and neuromelanin content.DiscussionThis protocol pioneers the integration of the QNT with advanced neuroimaging to elucidate its neuroplasticity mechanisms in PD, providing high-level mechanistic evidence for the integration of the QNT into PD care and optimizing integrative treatment strategies that combine traditional Chinese and Western medicine.Clinical trial registration(http://itmctr.ccebtcm.org.cn/), Identifier :ITMCTR2025000402.
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