研究疾病:
|
广泛性焦虑症
|
研究疾病代码:
|
|
Target disease:
|
Generalized anxiety disorder
|
Target disease code:
|
研究类型:
Study type:
|
干预性研究
Interventional study
|
研究设计:
Study design:
|
随机平行对照
randomized controlled trial(parallel group design)
|
研究所处阶段:
Study phase:
|
探索性研究/预试验
Pilot clinical trial
|
研究目的:
|
探究疏肝调神针法对GAD患者脑可塑性的影响,为针刺治疗GAD提供循证依据
|
Objectives of Study:
|
To explore the effect of acupuncture for soothing liver and regulating mind on brain plasticity in GAD patients and to provide evidence for acupuncture treatment of GAD
|
药物成份或治疗方案详述:
|
|
Description for medicine or protocol of treatment in detail:
|
|
纳入标准:
|
疫情下GAD患者纳入标准:
(1)符合上述广泛性焦虑症的中西医诊断标准,并于新冠疫情背景下确诊者;
(2)汉密尔顿焦虑量表 (HAMA) 14项测定≥14分且<29分者;
(3)年龄≥18岁,≤65岁;
(4)近三周内未接受过药物、物理或心理治疗者,或病情稳定者;
签署知情同意书,自愿参加本项研究者。
健康人群纳入标准:
(1)年龄≥18岁,≤65岁;
(2)右利手,性别不限;
(3)既往体健,近1个月无身体不适;
(4)近3个月未接受中枢刺激(rTMS、TDCS等)或外周刺激(针灸、经皮电刺激等);(5)无非法药物使用史及过量饮酒史;
(6)签署知情同意书,自愿参加本项研究者。
|
Inclusion criteria
|
Inclusion criteria of GAD patients under epidemic situation:
( 1 ) Patients who met the above diagnostic criteria of generalized anxiety disorder in Chinese and Western medicine and were diagnosed in the context of the new coronavirus epidemic ;
( 2 ) Hamilton Anxiety Scale ( HAMA ) 14 determination ≥ 14 points and < 29 points ;
( 3 ) Age ≥ 18 years, ≤ 65 years ;
( 4 ) those who have not received medication, physical or psychological treatment in the past three weeks, or those in stable condition ;
signed informed consent and volunteered to participate in this study.
Inclusion criteria for healthy people:
(1) Age ≥ 18, ≤ 65;
(2) Right handed, regardless of gender;
(3) He has been in good health without any discomfort in the past month;
(4) No central stimulation (rTMS, TDCS, etc.) or peripheral stimulation (acupuncture, transcutaneous electrical stimulation, etc.) in recent 3 months; (5) No history of illegal drug use and excessive drinking;
(6) Those who signed the informed consent form and volunteered to participate in the study.
|
排除标准:
|
疫情下GAD患者排除标准:
(1)不符合纳入标准的患者 ;
(2)既往有脑外伤、癫痫病史,或伴有肝肾功不全,有金属植入物或合并心脑血管、肝、肾等严重的躯体器质性疾病的患者;
(3)患有其他能够表现焦虑症状的精神分裂症、双相障碍或其他精神障碍类疾病、躯体疾病的患者;
(4)既往及当前有自伤自杀计划或行为、精神病性症状者或酒精、药物滥用或成瘾后戒断引起焦虑者;
(5)依从性可能较差或畏惧针灸者;
(6)左利手;
(7)妊娠及哺乳期妇女。
健康人群排除标准:
(1)有言语障碍者;
(2)有高血压、糖尿病及重大的心、肝、肾等脏器的疾患;(3)有痴呆、精神病、癒痫等神经系统病史;
(4)有颅脑外伤、手术史;
(5)体内有金属残留物者(包括义齿、起搏器、神经刺激器、医疗泵等);(6)对TMS畏惧及其它原因无法行TMS刺激者;
(7)妊娠妇女。
|
Exclusion criteria:
|
Exclusion criteria for GAD patients under epidemic situation:
( 1 ) Patients who do not meet the inclusion criteria ;
( 2 ) patients with a history of brain trauma, epilepsy, or accompanied by liver and kidney dysfunction, metal implants or severe physical organic diseases such as cardiovascular, cerebrovascular, liver and kidney ;
( 3 ) Patients with other anxiety symptoms of schizophrenia, bipolar disorder or other mental disorders, physical illness ;
( 4 ) Patients with previous or current suicide plan or behavior, psychotic symptoms or anxiety caused by alcohol, drug abuse or withdrawal after addiction ;
( 5 ) Patients with poor compliance or fear of acupuncture ;
( 6 ) Left-handed ;
( 7 ) Pregnant and lactating women.
Exclusion criteria for healthy population:
(1) People with speech disorder;
(2) Hypertension, diabetes and major heart, liver, kidney and other organ diseases; (3) Have a history of dementia, psychosis, epilepsy and other neurological diseases;
(4) History of craniocerebral trauma and operation;
(5) There are metal residues in the body (including dentures, pacemakers, nerve stimulators, medical pumps, etc.); (6) Those who are afraid of TMS and are unable to perform TMS stimulation for other reasons;
(7) Pregnant women.
|
研究实施时间:
Study execute time:
|
从From
2022-12-02
至To
2023-12-25
|
征募观察对象时间:
Recruiting time:
|
从From
2022-12-02
至To
2023-10-25
|