Clinical observation on the Treatment of Parkinson's Disease Related Fatigue with Fatigue three-needle

Authors
Category Primary study
Registry of TrialsInternational Traditional Medicine Clinical Trial Registry
Year 2025
INTERVENTION: Fatigue three‐needle acupuncture group:Basic treatment combined with Fatigue three‐needle acupuncture;Placebo‐acupuncture group:Basic treatment combined with placebo‐acupuncture; CONDITION: 8A00.0Z Parkinson's disease PRIMARY OUTCOME: Score of Multidimensional Fatigue Inventory.; SECONDARY OUTCOME: Score of Fatigue Severity Scale.;Score of Parkinson fatigue scale.;Score of Unified Parkinson's Disease Rating Scale.;Score of Parkinson's Patient Quality of Life Questionnaire.;Blood Plasma IL‐1ß content;Blood Plasma IL‐18 content;Blood Plasma TNF‐a content;Blood Plasma a‐syn content;Blood Plasma p‐a‐syn content; INCLUSION CRITERIA: (1) Gender is not limited, and the age is between 35 and 75 years old; (2) It meets the PDRF diagnostic criteria issued by MDS in 2016; (3) The modified Hoehn Yahr rating scale was rated 1‐3; (4) After dividing the total score of fatigue severity scale by 9, the final score is>4; (5) At present, the dosage of anti Parkinson's disease drug stabilizer is taken regularly for 1 month; (6) Normal mind, behavior coordination, clear language, and can correctly express the sense of acupuncture; (7) Good compliance, able to complete the test according to the requirements of the treatment plan, including those who can receive acupuncture treatment, follow‐up visits and follow‐up visits on time; (8) Voluntarily participate in the study and sign the informed consent. Only those who meet the above 8 requirements can be included.
Epistemonikos ID: 1cbdf6f7d1ef5d222a37a4d5da58d962d24b2ed6
First added on: Jan 24, 2026