Overview

Efficacy of Electroencephalography (EEG) Neurofeedback (NF) for the Treatment of Anxiety Disorder

Status:
Recruiting
Trial end date:
2023-11-01
Target enrollment:
0
Participant gender:
All
Summary
The aim of this study is to assess the efficacy of electroencephalography (EEG) neurofeedback (NF) as an Add-on Treatment for the Anxiety disorder. Meanwhile, evaluate the effect of EEG-NF on cognitive function of Anxiety patients. Furthermore, the investigators will examine the changes in cortisol, gut microbiome and some biomarkers. The hypothesis of this study is that EEG-NF alleviate the anxiety symptoms and improve the cognitive function of Anxiety disorder patients with regulating attention response.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Tianjin Anding Hospital
Treatments:
Antidepressive Agents
Antidepressive Agents, Tricyclic
Antipsychotic Agents
Hypnotics and Sedatives
Criteria
Inclusion Criteria:

- a current episode of Anxiety diagnosed according to Diagnostic and Statistical Manual
of Mental Disorders, Fifth Edition (DSM-5)

- age between 18 and 50 years

- a total score of HAMD ≥14 GAD-7≥ 5

- Participants are compliant with treatment according to the judgement of the treating
clinician.

- Participant or guardian has to sign informed consent. The patients' guardians will
sign the informed consent on behalf of the participants when the capacity of
participants to consent is compromised.

Exclusion Criteria:

- History of alcohol or drug abuse;

- Severe somatic diseases including conditions such as kidney and liver failure,
uncontrolled hypertension, cardiovascular, cerebrovascular and pulmonary disease,
thyroid disease, diabetes, epilepsy and asthma.

- Use of anti-inflammatory medication for longer than 7 days in the last two months
preceding the trial

- Use of immunosuppressive medication such as oral steroid hormones Women in pregnancy
or lactation period