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Brain Multimodal Magnetic Resonance Imaging study on the first night effect of Insomnia

Brain Multimodal Magnetic Resonance Imaging study on the first night effect of Insomnia

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100047013
Enrollment
Unknown
Registered
2021-06-07
Start date
2021-06-01
Completion date
Unknown
Last updated
2023-07-16

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

Conditions

Insomnia

Interventions

Control group:No

Sponsors

Peking Universality Sixth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Criteria for insomnia patients: insomnia that meets the diagnostic criteria of DSM-5 (Diagnostic and Statistical Manual of Mental Disorders, DSM); age 18-65, male or female, Han nationality, right-handed; junior high school and above, MMSE >=24 minutes; the daily bedtime in the past three months was between 9pm and 1am, and the daily bedtime every night>7 hours. 2. Standards for healthy sleepers: meet the standards for healthy sleepers reported in the literature [14]; 18-65 years old, male and female, Han nationality, right-handed; junior high school and above, MMSE>=24 points; within the past three months The daily bed time is between 9 pm and 1 am, and the daily bed time is >= 7 hours every night.

Exclusion criteria

Exclusion criteria: 1. It currently meets any common mental disorder (including major depressive episode, bipolar disorder, schizophrenia, alcohol or drug dependence, etc.); 2. Complicated with serious physical diseases or organic brain diseases; accompanied by other sleep disorders; night shifts in the first 3 months or travelers crossing two time zones; 3. Take drugs that affect sleep at least 2 weeks before participating in the test; pregnant or breastfeeding women; obese; those who are contraindicated in MRI examinations. Contraindications for MRI examinations include: subjects who have received cardiac pacemaker implantation, have grafts or metal foreign bodies in their bodies, have serious underlying diseases, and are claustrophobic subjects.

Design outcomes

Primary

MeasureTime frame
Insomnia severity scale;

Countries

China

Contacts

Public ContactHu Sifan

Peking University Sixth Hospital/Institute of Mental Health

husifan@bjmu.edu.cn+86 18811501577

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026