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Neural modulation of reward responsiveness deficits in adolescents with subthreshold depression

Neural modulation of reward responsiveness deficits in adolescents with subthreshold depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115670
Enrollment
Unknown
Registered
2025-12-30
Start date
2025-12-31
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Subthreshold depression

Interventions

Active (center-anode) group:The central anodal group receives high-definition transcranial direct current stimulation (HD-tDCS) with the anode placed at Fpz, at 1.5 mA for 20 minutes.
Sham group:The sham group receives HD-tDCS at Fpz with 1.5 mA stimulation for the initial 30 seconds, followed by a reduction to no more than 2 µA for the remainder of the session.

Sponsors

Institute of Psychology, Chinese Academy of Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 21 Years

Inclusion criteria

Inclusion criteria: 1.Conduct the MINI structured interview; currently does not meet ICD-11 diagnostic criteria for major depressive disorder; 2.Sex:male or female; 3.Age:18-21 years; 4.IQ:above 70; 5.No metallic implants in the body, meets functional near-infrared spectroscopy scanning conditions, and is willing to participate; 6.PHQ-9 self-rating scale score higher than 10.

Exclusion criteria

Exclusion criteria: 1.IQ<70. 2.Currently meets Major Depressive Disorder (M.I.N.I.) or is at high suicide risk. 3.History of epilepsy, stroke, traumatic brain injury, or cranial surgery. 4.Neurological disorders. 5.Substance abuse or alcohol dependence. 6.Use of psychotropic medication within the past 8 weeks. 7.Pregnancy. 8.Local scalp lesion/inflammation. 9.Cardiac pacemaker or metallic implants in the body. 10.Unremovable metal devices on the head. 11.Head injury. 12.For individuals with a history of epilepsy/cranial injury/stroke, inclusion is allowed only after careful evaluation even if recovery is self-reported. 13.Uncontrollable body movements (e.g., severe coughing, convulsions). 14.Chronic pain disorders with intake of analgesics such as aspirin or ibuprofen within the past 3 days. 15.Participation in other similar experiments within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Change in response bias (b') on the Probabilistic Reward Task (PRT) across pre-, mid-, and post-tDCS stages;Change in discriminability (d') on the Probabilistic Reward Task (PRT) across pre-, mid-, and post-tDCS stages;Change in oxyhemoglobin (?HbO) in the ventromedial prefrontal cortex (vmPFC) across pre-, mid-, and post-tDCS stages;

Secondary

MeasureTime frame
Change in reaction time on the Probabilistic Reward Task (PRT) across pre-, mid-, and post-tDCS stages;Change in accuracy on the Probabilistic Reward Task (PRT) across pre-, mid-, and post-tDCS stages;

Countries

China

Contacts

Public ContactHuang Jia

Institute of Psychology, Chinese Academy of Sciences

huangj@psych.ac.cn+86 10 6487 0528

Outcome results

None listed

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