Actively Recruiting

Age: 30Years - 80Years
All Genders
ID05524922

A Registered Observational Cohort Study on Neurodegenerative Associated With Sleep Disorder

Led by Fujian Medical University Union Hospital · Updated on 2025-01-22

500

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Cognitive problems often occur in people with neurodegenerative diseases. Researchers are exploring how sleep disorders relate to the progression of these diseases by studying their clinical signs, brain imaging, and biological markers. This observational study aims to better understand the mechanisms behind sleep problems in neurodegenerative conditions. Participants will have assessments including neuropsychological tests, brain MRI scans, and electroencephalograms. Biological samples will also be collected to measure markers like plasma Ab2-42 levels. These evaluations will help observe changes in sleep quality, cognitive function, heart rate variability, and other relevant outcomes over time. People in the study will undergo baseline and follow-up tests such as the Pittsburgh Sleep Quality Index (PSQI), Montreal Cognitive Assessment (MoCA), and Addenbrooke's Cognitive Examination (ACE-III). Researchers will monitor sleep patterns and biological markers to track disease progression. The study includes adults aged 30 to 80 years and will continue through June 2030, providing long-term data on sleep disorders linked to neurodegeneration.

CONDITIONS

Brief Title

A Registered Cohort Study on Neurodegenerative Associated With Sleep Disorder.

Who Can Participate

Age: 30Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of neurodegenerative disease.
  • Experience of insomnia, excessive drowsiness, or confusion at night.
  • Frequent awakenings, daily sleep episodes, or nocturnal confusion.
  • Presence of one or more: wandering at night with inappropriate activity, agitation or combativeness, confusion or marked delirium.
  • Polysomnographic monitoring showing poor sleep efficiency and increased number and duration of awakenings.
  • Multiple sleep latency tests showing increased daytime sleepiness.
  • Presence of other medical symptoms not indicating the primary disease.
  • Other sleep disorders may be present but do not explain main symptoms.
  • Diagnosis can be made based on any of the above.
Not Eligible

You will not qualify if you...

  • Patients with other neurological disorders.
  • Pregnant or lactating women.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Baseline

Participants undergo neuropsychological assessments, brain MRI, electroencephalogram, and biomarker data collection to evaluate neurodegenerative disorders associated with sleep disorders.

1 visit (in-person)

Long-term Monitoring

Duration - 1 year

Participants are monitored to observe changes in cognitive and sleep-related measures over time.

1 follow-up visit at 1 year after baseline

Trial Site Locations

Total: 1 location

1

Fujian Medical University Union Hospital

Fuzhou, Fujian, China, 350000

Actively Recruiting

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Research Team

X

Xiaodong Pan, Doctor

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

Frequently Asked Questions

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