Anxiety State Clinical Trial
Official title:
TCM Daoyin in the Treatment of Patients With Anxiety State: A Pilot Study
In recent years, the number of people with symptoms of anxiety are on the rise. TCM Daoyin is a promising intervention for anxiety. This study is designed to allow researchers to better understand the changes in anxiety symptom, brain activity, and immune function during patients with anxiety states receiving TCM Daoyin intervention. Thus, the aims of the prospective randomized study are: (1) to examine the effects of TCM Daoyin training on reducing symptoms of anxiety, (2) to measure brain activity by using functional magnetic resonance imaging (fMRI), and (3) to assess Immune function.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | August 31, 2024 |
Est. primary completion date | March 30, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Subject with a primary mental health complaint of anxiety. - Anxiety 14=HAMA-14=29, Depression 7=HAMD-17<14. - Subject has no history of psychotropic medication or has been off medication for more than 6 months. - Right-handed, aged 18 to 65, male or female. - Subject has a clear mind and the ability to lead an independent life. - Subject agrees to participate in fMRI scan and provide signed informed consent. Exclusion Criteria: - Subject with definite clinical diagnosis of anxiety disorder and depression disorder by ICD-10. - Subject with bipolar disorder, psychotic disorder (e.g., schizophrenia), organic mental disorder (e.g., Alzheimer's disease). - Subject with alcohol abuse, substance dependence and suicidal ideation in past-year, or currently taking psychiatric medication, or current serious suicidal attempt. - Subject with serious current unstable medical illness. - Subject has claustrophobia, or any contraindication unable or unwilling to participate in fMRI scan. - Subject is clinically unable to participate in TCM Daoyin training program. - Subject is pregnant or lactating women. |
Country | Name | City | State |
---|---|---|---|
China | Shanghai Qigong Research Institute | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Shanghai University of Traditional Chinese Medicine | Shanghai Mental Health Center |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 14-item Hamilton Anxiety Rating Scale | The 14-item Hamilton Anxiety Rating Scale (HAMA-14) is a clinician-rated assessment (structured interview) of patients' anxious symptoms. Questions focus on anxious symptoms during the past 7 days, and higher cumulative scores indicate more severe anxiety.
The HAMA-14 are rated on 5 grades ranging from 0(no symptom) to 4 (very severe). The total score ranges from 0 to 56. 29 or more on HAMA means severe anxiety disorders, 21 to 28 on HAMA means obvious anxiety disorders, 14 to 20 on HAMA means anxiety disorders, 8 to 13 on HAMA means suspicious anxiety disorders, 7 or less means no anxiety disorders. |
Change from Baseline HAMA-14 at 12 weeks | |
Secondary | 17-item Hamilton Depression Rating Scale | The 17-item Hamilton Depression Rating Scale (HAMD-17) is a clinician-rated assessment (structured interview) of patients' depressive symptoms. Questions focus on depressive symptoms during the past 7 days, and higher cumulative scores indicate more severe depression.
The HAMD-17 are rated on 5 grades ranging from 0(no symptom) to 4 (very severe). The total score ranges from 0 to 52. 25 or more on HAMD means severe depression disorders, 18 to 24 on HAMD means moderate depression, 13 to 17 on HAMD means mild depression disorders, 8 to 12 on HAMD means suspicious depression disorders, 7 or less means no depression disorders. |
Change from Baseline HAMD-17 at 12 weeks | |
Secondary | Depression, Anxiety and Stress Scale-21 item | The Depression, Anxiety and Stress Scale-21 item (DASS-21) is a self-rated assessment of patients' depressive, anxious and stress symptoms. Questions focus on depressive, anxious and stress symptoms during the past 7 days, and higher cumulative scores indicate more severe depression, anxiety and stress. Subscale scores are calculated as the sum of the responses to the seven items from each subscale multiplied by 2. The cutoffs for depression, anxiety, and stress are >9, >7, and >14, respectively. | Baseline | |
Secondary | Depression, Anxiety and Stress Scale-21 item | The Depression, Anxiety and Stress Scale-21 item (DASS-21) is a self-rated assessment of patients' depressive, anxious and stress symptoms. Questions focus on depressive, anxious and stress symptoms during the past 7 days, and higher cumulative scores indicate more severe depression, anxiety and stress. Subscale scores are calculated as the sum of the responses to the seven items from each subscale multiplied by 2. The cutoffs for depression, anxiety, and stress are >9, >7, and >14, respectively. | 6 weeks | |
Secondary | Depression, Anxiety and Stress Scale-21 item | The Depression, Anxiety and Stress Scale-21 item (DASS-21) is a self-rated assessment of patients' depressive, anxious and stress symptoms. Questions focus on depressive, anxious and stress symptoms during the past 7 days, and higher cumulative scores indicate more severe depression, anxiety and stress. Subscale scores are calculated as the sum of the responses to the seven items from each subscale multiplied by 2. The cutoffs for depression, anxiety, and stress are >9, >7, and >14, respectively. | 12 weeks | |
Secondary | Functional magnetic resonance imaging (fMRI) | The fMRI scans will be employed to assess whether engaging in TCM Daoyin training program does or does not alter structural imaging and functional imaging of brain activation. Changes in Blood Oxygen Level Dependent (BOLD) Response is investigated in resting state fMRI and task fMRI. | Baseline | |
Secondary | Functional magnetic resonance imaging (fMRI) | The fMRI scans will be employed to assess whether engaging in TCM Daoyin training program does or does not alter structural imaging and functional imaging of brain activation. Changes in Blood Oxygen Level Dependent (BOLD) Response is investigated in resting state fMRI and task fMRI. | 12 weeks | |
Secondary | Immune function | CD3, CD4, CD8, IL-1ß, IL-6 and TNF-a in blood samples will be measured to evaluate immune functions. | Change from Baseline immune function at 12 weeks | |
Secondary | Adverse effects | During the intervention period, the doctors will ask specifically about, and record any adverse effect of the treatment that may have occurred. | 6 weeks | |
Secondary | Adverse effects | During the intervention period, the doctors will ask specifically about, and record any adverse effect of the treatment that may have occurred. | 12 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05760482 -
Evaluation of the Relationship Between Bruxism and Tryptophan Metabolites
|
N/A | |
Recruiting |
NCT04368416 -
Anxiety/Depression, Sleep and Alcohol in Elderly Anxiety/Depression, Sleep Disturbances and Alcohol Use Disorder in Elderly With Cognitive Complaints
|
||
Completed |
NCT01190774 -
Anxiety Assessment Intervention in Dental Patients
|
Phase 2/Phase 3 | |
Not yet recruiting |
NCT06418269 -
The Effect of Therapeutic Play on Anxiety and Fear Levels in Children With Diabetes
|
N/A | |
Recruiting |
NCT06215456 -
Virtual Reality to Reduce Periprocedural Anxiety During Invasive Coronary Angiography
|
N/A | |
Completed |
NCT06114524 -
Effect of Binaural Beats on Level of Anxiety and Toleration in Patients Undergoing Upper Gastrointestinal Endoscopy Without Sedation
|
N/A | |
Completed |
NCT05316415 -
The Effects of Music on the Anxiety and Sleep Quality of Pregnant Women on Bed Rest for a High-risk Pregnancy
|
N/A | |
Recruiting |
NCT05433636 -
Mindful Waiting Room
|
N/A | |
Recruiting |
NCT06034496 -
Cranial Electrotherapy Stimulation and Acute Stress
|
N/A | |
Recruiting |
NCT06187090 -
The Supplementation Therapy in Autism and Response to Treatment Study
|
N/A | |
Completed |
NCT05499767 -
HEPPI: Efficacy of a Cognitive-Emotional Intervention for Homebound Older Adults
|
N/A | |
Not yet recruiting |
NCT03671317 -
Medical Clowns for Pediatric Blood Draw
|
N/A | |
Terminated |
NCT03227562 -
Is Initial Response to Low Dose Risperidone Predictive for Outcome in Anxiety?
|
Phase 3 | |
Completed |
NCT04040036 -
Effects of Virtual Reality on Pain, Fear and Anxiety During Blood Draw in Children Aged 5-12 Years Old
|
N/A | |
Completed |
NCT04568551 -
COVID-19-associated Anxiety of Pregnant Women for Anomalies, Stillbirth and Preterm Labor
|
||
Recruiting |
NCT06190184 -
Viome Precision Nutritional Programs to Improve Clinical Outcomes for Mental Health Conditions
|
N/A | |
Completed |
NCT04601545 -
The Virtual Reality Therapy as a Pulmonary Rehabilitation Supporting Method
|
N/A | |
Completed |
NCT06223412 -
Visual Based Program and Climate Change
|
N/A | |
Recruiting |
NCT04356638 -
a Phase III Trial of Safety and Efficacy of Premedication With Dexmedetomidine and Midazolam in Pediatric Patients
|
Phase 3 | |
Completed |
NCT03977948 -
Qualitative and Systemic Assessment of a Nurse Intervention an Inpatient Child and His or Her Parents
|