Yong Tang
Chengdu, Sichuan, 610075, China
NCT Number: NCT01055561
The purpose of the study is to evaluate the safety and tolerability of acupuncture for patients with BPSD & healthy volunteers.
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Notify Me60 year–85 year
All sexes
Interventional
Phase 1
Chengdu, Sichuan, 610075, China
This open label study is designed to evaluate the safety and tolerability of acupuncture as a intervention for patients with Behavioral and Psychological Symptoms of Dementia (BPSD)& healthy volunteers,and this study will enroll a total of 30(15 patients,15healthy volunteers) patients who are suffered from BPSD or healthy volunteers.The patients who have to be suitable for the standard of inclusion criteria will be included,and who have one condition of the exclusion criteria will be excluded,and so do the healthy volunteers.For each enrolled participant will obtain a baseline psychiatric and medical assessment, results of the Mini-Mental Status-Evaluation (MMSE),Behavioral Pathology in Alzheimer's Disease Rating Scale(BEHAVE-AD),Activity of Daily Living Scale(ADL)and other basic information prior to beginning acupuncture.For each participant will get acupuncture which once a day for 7 days running. During the trial the Questionnaire of Acupuncture-related Events have to be evaluated every day, and at the end of the intervention,all of the MMSE,BEHAV-AD,ADL and Treatment Emergent Symptom Scale (TESS)will be investigated.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
The eligibility criteria of the patients arm:
Inclusion criteria
Exclusion criteria
The eligibility criteria of the healthy volunteers arm:
Inclusion criteria
Exclusion criteria
Participators will be stimulated at specific acupuncture points as determined for the disease by the professional acupuncturists, and acupuncture once a day,last for one week.
Other names: Complementary and Alternative Medicine, Traditional Chinese Medicine
Time frame: Every day during a 7 days trial
Time frame: Baseline and 1week after the trial begen
Time frame: Baseline and 2 weeks after the trial begen
Chengdu University of Traditional Chinese Medicine
Other
An Open-label Multi-center Safety and Tolerability Study of Acupuncture for Patients With Behavioural and Psychological Symptoms of Dementia & Healthy Volunteers
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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