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Temporal Memory in Schizophrenic Patients

Transcranial Electrical Stimulation Combined With Interim Testing Promotes Temporal Memory in Patients With Schizophrenia

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06562504
Enrollment
75
Registered
2024-08-20
Start date
2024-08-15
Completion date
2024-09-30
Last updated
2024-08-20

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

Conditions

Patients With Schizophrenia

Brief summary

Temporal order memory deficits are a central feature of cognitive abnormalities in schizophrenia. The dorsolateral prefrontal cortex contributes to the extraction of temporal contextual information. Transcranial direct current stimulation (tDCS) and interim testing have been shown to be external techniques that can improve temporal order memory deficits in schizophrenia patients. Transcranial alternating current stimulation (tACS) can also improve cognitive functioning in patients with schizophrenia. This study intends to investigate the learning effects of temporal order memory under two learning strategies during tDCS targeting the left dorsolateral prefrontal cortex (L-DLPFC) and transcranial direct current stimulation (tDCS) interventions in patients with schizophrenia, to investigate whether it can promote the retention of temporal order memory in patients, and to compare the differences in the effects of the two intervention modalities. This study was planned to recruit 75 patients diagnosed with schizophrenia from the hospital. A single online tDCS (2 mA × 20 min) and tACS (1.5 mA × 20 min, theta rhythm) intervention was conducted during which participants performed a temporal-sequence memory task for visual pictures, and test scores were compared for each stimulus type on an intermediate test and repetition of the two strategies of learning.

Detailed description

Treatment was conducted by two examiners, and participants' memory levels were tested before the start of the experiment using a flanker task and a numerical breadth task as baseline tests. The experimental procedure was divided into a learning phase, in which participants memorized the sequence of pictures, and a testing phase, in which participants were required to recall a picture presented after the probe item. Participants were randomly assigned in parallel to each stimulus type and learning strategy, with 25 receiving tdcs anodized stimuli, 25 receiving sham stimuli, and another 25 receiving tacs stimuli. And participants' inhibitory control continued to be tested using the flanker task before and after the stimuli for pre- and post-intervention comparisons.

Interventions

DEVICETranscranial direct current stimulation (tDCS)- anodal group

2mA/20mins/session;

DEVICETranscranial direct current stimulation (tDCS)- sham group

0mA/20mins/session

DEVICEtranscranial alternating current stimulation (tACS)-tACS group

1.5 mA/20 min/session; 6HZ, theta

Sponsors

Xiaofeng Ma
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

1. Meeting the diagnostic criteria for schizophrenia according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5); 2. Aged 18 years or older, regardless of gender, with an educational level of elementary school or above; 3. All patients received stable-level antipsychotic medication treatment, were in a stable phase of disease treatment, able to understand the testing requirements, and cooperated to complete all research tasks; 4. No history of neurological disorders or other serious physical illnesses, and no history of intellectual disability; 5. No color blindness, color weakness, or other color vision impairments, with normal vision or corrected vision.

Exclusion criteria

1. Clear cognitive impairment caused by somatic or cerebral organic lesions, such as cerebrovascular diseases, traumatic brain injury, etc; 2. Individuals with mental disorders caused by substance dependence or abuse, or the use of psychoactive substances; 3. History of brain injury or other central nervous system-related organic diseases; 4. Individuals at significant risk of suicide or harming others; 5. Participation in similar experiments in the past 30 days prior to baseline.

Design outcomes

Primary

MeasureTime frameDescription
Correctness of temporal recall5mins to 24 hoursStimulus content was presented using the Eprime experimental program, and participants pressed key responses during the test phase to record their rate of correctness. Stimulus content was presented using the Eprime experimental program, and participants pressed key responses during the test phase to record their rate of correctness.
proactive interference rate5mins to 24 hoursThe rate of intrusion of prior information when participants recalled the current information was counted.

Countries

China

Contacts

Primary ContactTiantian Li, Doctor
psylitiantian@outlook.com13909483531

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026