Digital cognitive intervention for high-risk dementia populations
Impact of the Digital Multi-domain Cognitive Intervention in High-risk Populations for Dementia
This study is testing a new digital program that combines education, exercise, art, and brain training to see if it can help people with early signs of memory problems and reduce their risk of developing dementia.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 128 (estimated) |
| Ages | 55 Years and up |
| Sex | All |
| Sponsor | Fujian Provincial Hospital Academic / other |
| Locations | 1 site (Fuzhou, Fujian) |
| Trial ID | NCT06442943 on ClinicalTrials.gov |
What this trial studies
This study focuses on developing and testing a digital multimodal cognitive intervention program aimed at individuals with Mild Cognitive Impairment (MCI) or Subjective Cognitive Decline (SCD). The intervention combines health education, exercise, art activities, and cognitive training to assess its feasibility, effectiveness, and safety. By conducting randomized controlled trials, the study seeks to provide early detection and intervention strategies for dementia, particularly Alzheimer's Disease, which is increasingly prevalent in China.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals diagnosed with Mild Cognitive Impairment or Subjective Cognitive Decline who can communicate in Mandarin.
Not a fit: Patients with advanced dementia or severe physical illnesses that hinder participation may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly delay or prevent the progression of dementia in high-risk populations.
How similar studies have performed: Other studies have shown promise in using cognitive interventions for dementia prevention, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * MCI (refer to Peterson's diagnostic criteria) or SCD (refer to the diagnostic framework proposed by Jak bondi and Jessen et al.); * Able to communicate normally in Mandarin; * Certain level of comprehension and judgment abilities, aware of the purpose of the survey and consents to participate. Exclusion Criteria: * Patients with dementia exhibiting abnormal mental behavior; * Individuals with severe hearing or speech impairments; * Those with serious physical illnesses who are unable to cooperate and complete the survey.
Where this trial is running
Fuzhou, Fujian
- Fujian Provincial Hospital — Fuzhou, Fujian, China (Recruiting)
Study contacts
- Study coordinator: lian fayang, MD
- Email: fjslkyk@163.com
- Phone: 0591-87557768
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.