depression
Conditions
Interventions
Intervention group:The intervention lasted for two weeks, during which participants engaged in the ABM intervention treatment twice daily via an online platform, totaling 10sessions.
Control group:The placebo group was identical to the ABM condition in every respect except the probe position, which was in the same location of the negative stimulus in 50 percent of trials and in th
Sponsors
Central China Normal University
Eligibility
Sex/Gender
All
Age
25 Years to 19 Years
Inclusion criteria
Inclusion criteria: All experimental participants were right-handed, free from mental illness, neurological trauma, or severe physical diseases, and had normal or corrected-to-normal vision. The inclusion criteria for participants with depression tendencies were: a DASS-21 score >= 14. Healthy control participants were matched with the depression group in terms of age, gender, and education level, and all had DASS-21 scores < 14.
Exclusion criteria
Exclusion criteria: Eligibility criteria included the absence of mental illness, neurological trauma, or severe physical diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| depression;ERP;Attention Bias; | — |
Countries
China
Contacts
Public ContactLin Zhang
Central China Normal University
Outcome results
None listed