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An association study of periodic circadian rhythm differences with stress and emotional tendencies based on objective measurements

An association study of periodic circadian rhythm differences with stress and emotional tendencies based on objective measurements

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090004
Enrollment
Unknown
Registered
2024-09-23
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

anxiety/depressive symptoms

Interventions

Observation group (Grouping based on different circadian rhythm):None

Sponsors

Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.Informed and written consent. 2.Age =18 years old, male or female. 3.Normal general health, able to understand and comply with study requirements.

Exclusion criteria

Exclusion criteria: 1.Current or previous diagnosis of bipolar disorder, schizophrenia, schizoaffective disorder, neurodevelopmental disorder, neurocognitive disorder according to DMS-5 diagnostic criteria. 2.The patient is currently at significant suicide risk, with a score of = 3 on the HAMD-24 suicide risk item. 3.Special lighting conditions in the working or living environment, including but not limited to basements, dark rooms, tunnels, and studios; or working night shifts for a long time, working across time zones, etc. 4.Use of sedative-hypnotic drugs or other antidepressant, anxiolytic, and antipsychotic drugs within the past 3 months; History of alcoholism, smoking, and other psychoactive substance abuse within the past 3 months. 5.Have used medication to assist sleep in the past 3 months. 6.Current or previous sleep disorders (e.g., restless legs syndrome, etc.). 7.Current or prior suffering from any serious injury, medical or psychological illness that may preclude completion of the trial, including severe cardiovascular, respiratory disease such as stroke; endocrine diseases such as hyperthyroidism; recent surgery; acute or chronic pain; Dementia, traumatic brain injury, etc. 8.Exclude a history of other systemic major diseases. 9.Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
sleep quality;Anxiety/Depression level;Biological rhythms;

Secondary

MeasureTime frame
wearable devices to monitor physical activity;demographic information;blood biochemical indicators;genetic;metabolomics;dietary information;gut microbiota;anthropometric indices;

Countries

China

Contacts

Public ContactLiang Sun

Fudan University

sun_liang@fudan.edu.cn+86 21 5423 7087

Outcome results

None listed

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