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Study on Psychological, Behavioral, and Magnetic Resonance Brain Functional Changes in SLE Patients

Study on Psychological, Behavioral, and Magnetic Resonance Brain Functional Changes in SLE Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120244
Enrollment
Unknown
Registered
2026-03-11
Start date
2026-03-27
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Systemic lupus erythematosus

Interventions

Healthy Control Group:None

Sponsors

The First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1.Meeting the 1997 classification criteria for systemic lupus erythematosus (SLE) recommended by the American College of Rheumatology (ACR) or the 2009 ACR classification criteria for SLE; 2.Aged 18–50 years; 3.Educational level of primary school or above, proficient in Mandarin Chinese with capacity to comprehend scale contents, and capable of completing the questionnaires; 4.Signed informed consent by the patient and their guardian. Control group: 1. Age and gender matched with patients; 2. Voluntarily participate in this study; 3. Age 18-50 years; 4. Elementary school education or above

Exclusion criteria

Exclusion criteria: 1.Diagnosed with schizophrenia, mental retardation, alcohol abuse, alcohol dependence, or other psychoactive substance dependence; 2.History of major organic brain diseases, including trauma, tumor, stroke, infection, contagious disease, epilepsy, or definite neurodegenerative disorders; comorbid with other autoimmune diseases meeting ACR classification criteria for rheumatoid arthritis, systemic sclerosis, Sjögren's syndrome (primary or secondary), other connective tissue diseases, or drug-induced SLE; 3.Patients with severe cardiac, hepatic, renal, or pulmonary insufficiency; 4.Women who are pregnant, lactating, or planning pregnancy; 5.Patients with MRI contraindications, such as implanted vascular stents, pacemakers, metal dentures, hearing aids, etc.; or patients with claustrophobia; 6.Patients with previous clinical conditions potentially causing brain atrophy (stroke, hypertension, diabetes mellitus, drug or alcohol dependence). Control Group: 1. Individuals with a family or personal history of significant somatic diseases; 2. Individuals with a family or personal history of immune system disorders; 3. Individuals with a family or personal history of neuropsychiatric disorders; 4. Individuals with a history of substance abuse, screened by an experienced psychiatrist using the DSM-IV Structured Clinical Interview for Non-Patient Version.

Design outcomes

Primary

MeasureTime frame
Self-report scales scores: Symptom Checklist-90, Self-Rating Anxiety Scale, Self-Rating Depression Scale , 36-Item Short Form Health Survey, Fatigue Severity Scale; ;sMRI, fMRI, and DTI data; SLE-related autoantibodies, cytokines, and absolute lymphocyte subset count analysis.;Clinician-administered scale scores : Hamilton Anxiety Rating Scale, Hamilton Depression Rating Scale,Montreal Cognitive Assessment;;

Countries

China

Contacts

Public ContactBai Ru

The First Affiliated Hospital of Kunming Medical University

76266814@qq.com+86 871 65324888

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026