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Individually-tailored intervention strategy and risk staging prognostic system for progression from mild cognitive impairment to alzheimer's disease

Individually-tailored intervention strategy and risk staging prognostic system for progression from mild cognitive impairment to alzheimer's disease

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022287
Enrollment
Unknown
Registered
2019-04-03
Start date
2019-04-03
Completion date
Unknown
Last updated
2019-04-08

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

Conditions

mild cognitive impairment

Interventions

Group 1:real rTMS interventions
Group 2:Pseudo rTMS Interventions
Group 3:real rTMS and cognitive training interventions
Group 4:Pseudo rTMS and cognitive training interventions
Group 5:Cognitive training interventions
Placebo group:Placebo
Contol group:No intervention

Sponsors

the Affiliated Brain Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. subjective memory impairment corroborated by the subject and an informant; 2. objective memory performance documented according to an Auditory Verbal Memory Test-delayed recall score that was within = 1.5 SD of age- and education-adjusted norms (the cutoff was = 4 correct responses on 12 items for = 8 years of education); 3. normal general cognitive function as evaluated by a MMSE of 24 or higher; 4. a Clinical Dementia Rating of 0.5, with at least a 0.5 in the memory domain; no or minimal impairment in daily living activities.

Exclusion criteria

Exclusion criteria: 1. a past history of known stroke (modified Hachinski score of > 4), alcoholism, head injury, Parkinsons disease, epilepsy, major depression (excluded by Self-Rating Depression Scale), or other neurological or psychiatric illness (excluded by clinical assessment and case history); 2. major medical illness (e.g., cancer, anemia, and thyroid dysfunction); 3. severe visual or hearing loss; 4. T2-weighted MRI showing major white matter (WM) changes, infarction, or other lesions (two experienced radiologists analyzed the scans); 5. dementia meets the criteria of the National Institute of Neurological and Communicative Disorders and Stroke or the AD and Related Disorders Association criteria for AD.

Design outcomes

Primary

MeasureTime frame
MoCA;MMSE;CDR;ADAS;MDRS;CARE index;Functional connectivity;Gray Matter;White matter integrity;Functional Network;Hippcampus;Structural Network;

Countries

China

Contacts

Public ContactJiu Chen

the Affiliated Brain Hospital of Nanjing Medical University

ericcst@aliyun.com+86 18751997338

Outcome results

None listed

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