CTA-MCI: Cognitive Control Training in Patients With Amnestic Mild Cognitive Impairment(CTA-MCI)
- Conditions
- Amnestic Mild Cognitive Impairment
- Interventions
- Behavioral: internet-based adaptive cognitive control training programBehavioral: placebo program
- Registration Number
- NCT03133052
- Lead Sponsor
- First Affiliated Hospital of Zhejiang University
- Brief Summary
This study evaluates the efficacy and mechanism of internet-based cognitive control training on episodic memory function in patients with amnestic Mild Cognitive Impairment(aMCI). Half of participants will receive adaptive internet-based cognitive control training program, while the other half will receive a fixed, primary difficulty level task.
- Detailed Description
Background:
Alzheimer's disease (AD) is a common dementia in elderly populations, and amnestic mild cognitive impairment (aMCI) refers to a transitional stage between normal aging and early dementia. Patients with aMCI are at higher risks of evolving toward AD. Although it has been widely recognized that early intervention of aMCI holds the potential to delay or even reverse the cognitive impairment, no treatment is available yet. Episodic memory dysfunction is the characteristic impairment in aMCI, cognitive control training significantly improved executive function in patients with aMCI . Whether and how cognitive control training improves episodic memory function in patients with aMCI remains largely unknown.
Objectives:
The primary objective of this double-blinded, randomized RCT is to assess whether internet-based cognitive control training in patients with amnestic Mild Cognitive Impairment improves their episodic memory function. The second objective is to evaluate the effect of cognitive control training on neural plasticity, including brain activation and white matter integrity, which are assessed by functional and structural MRI.
Patients and Methods:
The proposed study is a single-center, double-blinded, randomized controlled trial that will include 70 patients diagnosed with aMCI from the neurology clinics at The First Affiliated Hospital, Zhejiang University. The patients will be randomized to either a training or a control group. The intervention is internet-based cognitive control training performed for 30 minutes over 60 sessions. Neuropsychological assessment and functional magnetic resonance imaging (MRI) will be performed before and 12 weeks after training.
Relevance:
Currently there is no known treatment available for aMCI. The proposed study is to determine the efficacy of cognitive control training on episodic memory function in patients with aMCI. Secondly, using functional and structural MRI, this study is to reveal the potential mechanism underlying cognitive control training.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 70
- Literate Chinese, aged 50 years and older
- Complaint about memory loss and confirmed by an informant
- Cognitive impairment in memory domain, adjusted for age and education
- Normal or near-normal performance on general cognitive function and no or minimum impairment of daily life activities
- Clinical dementia rating (CDR) =0.5, Mini-Mental State Examination (MMSE) score ≥ 20 (primary school) or ≥ 24 (junior school or above)
- Failure to meet the criteria for dementia
- history of clinically significant stroke
- neurological diseases that may lead to neurological distortion, including schizophrenia, severe anxiety or depression, frontotemporal dementia，Huntington disease, brain tumor, parking disease, metabolic encephalopathy, encephalitis, multiple sclerosis, epilepsy, brain trauma, normal pressure hydrocephalus
- systemic diseases that may lead to neurological distortion, including hypothyroidism, folic acid deficiency, vitamin B12 deficiency, severe anemia, specific infection such as HIV and syphilis
- clinically significant gastrointestinal, renal, hepatic, respiratory, endocrine, or cardiovascular system disease;
- cancer, alcoholism, drug addiction;
- severe aphasia, physical disabilities, or any other factor that may preclude completion of neuropsychological testing;
- use of medications that may affect cognitive functioning, including tranquilizers, anti-anxiolytics, hypnotics, nootropics, and cholinomimetic agents;
- inability to undergo a brain MRI.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description training group internet-based adaptive cognitive control training program Intervention: Internet-based adaptive cognitive control training program. 5 x 30 minutes per week, for 12 weeks. control group placebo program Intervention: placebo program: a fixed, primary difficulty level task. 5 x 30 minutes per week, for 12 weeks.
- Primary Outcome Measures
Name Time Method Montreal Cognitive Assessment (MoCA) 12 weeks The study uses MoCA to assess changes in the global cognitive function after an intervention of cognitive control training
Auditory Verbal Learning Test (AVLT) 12 weeks The study uses AVLT to assess changes in the episodic memory function after an intervention of cognitive control training
- Secondary Outcome Measures
Name Time Method White matter Integrity 12 weeks The study uses Diffusion tensor imaging and tracking (DTI) to measure changes of the Integrity of white matter after an intervention of cognitive control training
Brain response change 12 weeks The study uses task functional MRI (fMRI) to measure the brain response changes during the task after an intervention of cognitive control training
Functional connectivity across regions 12 weeks The study uses resting state functional MRI(rs-fMRI) and task fMRI to measure changes of functional connectivity across regions after an intervention of cognitive control training
Gray matter volume 12 weeks The study uses voxel-based morphometry (VBM) to measure changes of gray matter volume after an intervention of cognitive training.
Trial Locations
- Locations (1)
The First Affiliated Hospital, Zhejiang University
🇨🇳Hangzhou, Zhejiang, China