Skip to content

Risk Factors of Anxiety and Depression in Patients With Herpes Zoster Neuralgia

Risk Factors Analysis of Anxiety and Depression in Patients With Herpes Zoster Neuralgia and Characteristics of Serum Biomarkers and Functional Brain Magnetic Resonance Changes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06449547
Enrollment
600
Registered
2024-06-10
Start date
2024-06-21
Completion date
2026-12-31
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Herpes Zoster

Keywords

Anxiety, Depression, Herpes Zoster, Neuralgia

Brief summary

The goal of this observational study is to explore risk factors of anxiety and depression in patients with herpes zoster neuralgia, and the changes of certain serum biomarkers and functional brain magnetic resonance images of these patients.

Detailed description

Patients with herpes zoster neuralgia will be recruited and take Hospital anxiety depression rating scale (Hospital anxiety and 'scale, HADS) evaluation. According to the HADS Scores, patients will be divided into depression group and no depression, or anxiety group and no anxiety group. The clinical data the of two groups will be collected and statistically analyzed to explore the risk factors of anxiety and depression, including the changes of serum biomarkers and functional brain magnetic resonance imaging in patients with herpes zoster neuralgia accompanying anxiety or depression.

Interventions

DIAGNOSTIC_TESTHospital Anxiety and Depression Scale

Hospital Anxiety and Depression Scale questionnaire is used to test patients for anxiety and depression.

Sponsors

Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age more than 18 years old 2. Diagnosed as herpes zoster neuralgia 3. Signing informed consent

Exclusion criteria

1. Unable to complete the scale assessment 2. History of mental illness

Design outcomes

Primary

MeasureTime frameDescription
HADS scoreduring hospital stay, average of 1 weekEnrolled patients will be first evaluated by Hospital Anxiety and Depression Scare questionaire and according to the HADS score, patients will be divided to group with anxiety/depression and group without anxiety/depression.

Secondary

MeasureTime frameDescription
IL-2 receptor plasma levelduring hospital stay, average of 1 weekBlood sample will be obtained from enrolled patients and the plasma level of inflammatory cytokines IL-2 (u/ml)will be tested.
IL-6 plasma levelduring hospital stay, average of 1 weekBlood sample will be obtained from enrolled patients and the plasma level of inflammatory cytokines IL-6 (pg/ml)will be tested.
IL-8 plasma levelduring hospital stay, average of 1 weekBlood sample will be obtained from enrolled patients and the plasma level of inflammatory cytokines IL-8 (pg/ml)will be tested.
IL-10 plasma levelduring hospital stay, average of 1 weekBlood sample will be obtained from enrolled patients and the plasma level of inflammatory cytokines IL-10 (pg/ml)will be tested.
Interleukin (IL)-1β plasma levelduring hospital stay, average of 1 weekBlood sample will be obtained from enrolled patients and the plasma level of inflammatory cytokines IL-1β (pg/ml)will be tested.
Brain-derived neurotrophic factor (BDNF) plasma levelduring hospital stay, average of 1 weekBlood sample will be obtained from enrolled patients and the plasma level of BDNF(pg/ml)will be tested.
C-reactive protein (CRP) plasma levelduring hospital stay, average of 1 weekBlood sample will be obtained from enrolled patients and the plasma level of CRP(mg/ml)will be tested.
Area under curve (AUC) of topological metrics of functional brain magnetic resonance imagingduring hospital stay, average of 1 weekFunctional brain magnetic resonance imaging will be performed in patients with anxiety or depression, and area under curve (AUC) of topological metrics including Eglob,Eloc,Cp,Lp,γ,λ and σ will be calculated and analyzed.
Interferon(INF)-α plasma levelduring hospital stay, average of 1 weekBlood sample will be obtained from enrolled patients and the plasma level of inflammatory cytokines INF-α (pg/ml)will be tested.

Countries

China

Contacts

Primary ContactYang Shuguang, M.D
yangsuperpro@163.com(+86)15071078161
Backup ContactMei wei, M.D, PhD
wmei@hust.edu.cn(+86)13006162508

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026