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The impact of sleep deprivation on social decision-making in different situations

The impact of sleep deprivation on social decision-making in different situations

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047062
Enrollment
Unknown
Registered
2021-06-07
Start date
2021-05-27
Completion date
Unknown
Last updated
2022-01-18

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

Conditions

sleep deprivation

Interventions

Experimental group1:phase I: normal sleep
Experimental group2:phase I: sleep deprivation

Sponsors

Peking University Sixth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 26 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 26 years,right handed; 2. Education level: college education level or above; 3. Regular sleep habits (6.5 to 9 hours) score less than 7 on the Pittsburgh Sleep Quality Index Scale; 4. The degree of myopia less than 800, astigmatism less than 100, and the correction degree is normal; 5. Signed the written informed consent and volunteered to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Having symptoms or history of psychiatric disorder, physical disorder or sleep disorder; No medications within 3 months prior to the study. 2.Previous medication history and physical therapy that affected the neuropsychiatric system within 1 month prior to the trial: When enrolled, the investigator will carefully ask the subjects about all medications taken within 1 month prior to the trial, and the investigator will judge the medication use. Physical therapy includes transcranial magnetic stimulation (TMS), transcranial electrical stimulation (TESS), traditional Chinese acupuncture therapy and so on; 3.Patients with the following diseases: Cerebrovascular disease Coronary artery insufficiency Recent myocardial infarction Raynaud's disease Chronic renal dysfunction Sinoatrial node or atrioventricular node dysfunction Thromboangiitis obliterans; 4.Have a history of epilepsy and a family history; 5.Patients with contraindications to MRI scanning; 6.Smokers; 7.Transmeridian travel or shift work or irregular sleep-wake rhythms during the 60 days prior to the experiment; 8.Students majoring in psychology and economics and finance; 9.Drink more than 3 cups of coffee a day; 10.Non-compliant participants; 11.Women during pregnancy and lactation.

Design outcomes

Primary

MeasureTime frame
indebtedness;social discounting;Moral opportunism;Magnetic resonance signal;

Secondary

MeasureTime frame
Sleep diary;Polysomnography;Morning and Evening Questionnaire-5;Epworth Sleepiness Scale;Pittsburgh Sleep Quality Index;Karolinska Sleepiness Scale;Self-Rating Anxiety Scale;Self-rating depression scale;State-Trait Anxiety Inventory;Mini-International Neuropsychiatric Interview;Repeatable Battery for the Assessment of Neuropsychological Status;Interpersonal Reactivity Index;Guilt and Shame Proneness Scale;Dispositional Greed Scale;Communal Orientation Scale;Exchange Orientation Scale;State Self-Control Capacity Scale;The Positive and Negative Affect Scale;The Slider Measure;The Positive and Negative Affect Scale;Psychomotor Vigilance Task;Operation Span Task;

Countries

China

Contacts

Public ContactSun Hongqiang

Peking University Sixth Hospital

sunhq@bjmu.edu.cn+86 10 82805960

Outcome results

None listed

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