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The Role of Sleep Memory Editing in Emotional-Cognitive Dysfunction in Depression

The Role of Sleep Memory Editing in Emotional-Cognitive Dysfunction in Depression

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123378
Enrollment
Unknown
Registered
2026-04-26
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Major Depression Disorder

Interventions

Interference group:Positive Cue-Targeted Memory Reactivation
Extinction group:Negative Cue-Targeted Memory Reactivation
Neutral Control Group:Neutral Cue-Targeted Memory Reactivation

Sponsors

Beijing HuiLongGuan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1.Meeting the diagnostic criteria for depression according to DSM-5; 2. All patients have undergone rigorous clinical testing and medical history review, with no history of manic, mixed, or hypomanic episodes during the entire disease course, the current diagnosis is unipolar depressive episode; 3.Aged 12–25 years, with no reading or writing impairment in Chinese; 4. Body Mass Index (BMI) not exceeding the age- and gender-specific overweight standards as defined in the "Guidelines for Weight Management" (2024 edition); 5.Normal or corrected-to-normal vision; 6. Voluntary participation in the study, with signed informed consent; 7.No history of electroconvulsive therapy in the past six months; 8.Right-handed.

Exclusion criteria

Exclusion criteria: 1. Presence of severe sleep-onset problems: In the past week, experiencing sleep latency >1.5 hours for more than 2 days, single-day sleep latency >3 hours, nighttime awakenings >2 times, average nighttime sleep duration <6 hours, or single-day nighttime sleep duration <5 hours; 2.Comorbidity with obstructive sleep apnea syndrome or restless legs syndrome; 3.Previous history of neurological disorders, alcohol or drug abuse; 4.Previous diagnosis or current suspicion of schizophrenia spectrum disorders; 5. Impulsive excitement, severe deterioration, or uncooperativeness; 6.Presence of suicidal behavior or severe suicidal ideation; 7.Serious physical illness or drug side effects; 8.Inability to cooperate with the study due to personal reasons or functional decline.

Design outcomes

Primary

MeasureTime frame
Image Emotion-Cognitive Valence;Picture Recognition Memory Accuracy;

Countries

China

Contacts

Public ContactShuping Tan

Beijing HuiLongGuan Hospital

shupingtan@sina.com+86 10 83024485

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026