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Construction of a Quantitative Cognitive Load System Based on Naturalistic Film Ratings and Analysis of Brain Network Response Mechanisms

Construction of a Quantitative Cognitive Load System Based on Naturalistic Film Ratings and Analysis of Brain Network Response Mechanisms

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108875
Enrollment
Unknown
Registered
2025-09-08
Start date
2025-09-08
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Patients with cognitive disorders

Interventions

Healthy Control group (study 1,Can be shared with Study 1):None
Healthy Control group (study 2):None
Mild Cognitive Impairment patient group (study 2):None
Mild Cognitive Impairment patient group (study 3):Non-invasive brain stimulation (NIBS)

Sponsors

Department of Rehabilitation Medicine, Sir Run Run Hospital, Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18-80 years old 2.Gender: No specific restrictions, but the study aims to balance gender (e.g., approximately 50% male and 50% female) to control for gender bias. 3.Study 1: No cognitive impairment (MoCA score >= 26) 4.Studies 2 & 3: Presence of cognitive impairment (MoCA score < 26, including but not limited to Alzheimer's disease, mild cognitive impairment, vascular cognitive impairment, traumatic brain injury, etc.)

Exclusion criteria

Exclusion criteria: 1.Presence of severe visual, hearing, or speech impairments that prevent effective communication, inability to cooperate, or refusal to participate. 2.Unstable medical conditions, such as severe pulmonary or cardiac diseases, history of liver or kidney failure or malignant tumors, or presence of proximal deep vein thrombosis in the lower limbs. 3.History of psychiatric or psychological disorders: e.g., schizophrenia, bipolar disorder, depression, etc. 4.Long-term use of medications that may affect neurological or cognitive function (applies to healthy participants). 5.History of major surgery or hospitalization within the past 6 months (applies to healthy participants). 6.Significant psychological stress triggered by major life events (e.g., bereavement, unemployment) within the past 3 months. 7.Participation in other clinical trials or interventional studies that may interfere with the results within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Task-related HbO2 concentration changes (changes in cerebral blood flow).;Resting-state functional connectivity strength.;Heart rate variability;Montreal Cognitive Assessment (MoCA);Cognitive Load;Arousal;

Countries

China

Contacts

Public ContactLin Feng

Department of Rehabilitation Medicine, Sir Run Run Hospital, Nanjing Medical University

peterduus@njmu.edu.cn+86 138 5144 6615

Outcome results

None listed

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