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Construction and effectiveness evaluation of a sleep restriction intervention program for older adults with mild cognitive impairment with insomnia in the community

Construction and effectiveness evaluation of a sleep restriction intervention program for older adults with mild cognitive impairment with insomnia in the community

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083712
Enrollment
Unknown
Registered
2024-04-30
Start date
2024-05-02
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

mild cognitive impairment

Interventions

Sleep restriction group:The sleep restriction group used sleep restriction intervention, which consisted of two main components, sleep restriction and sleep and cognitive health education.
Health Education Group:Using the same health education as the sleep restriction group

Sponsors

Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: (i) age = 60 years old; (ii) meeting the diagnostic criteria for both MCI and insomnia; (iii) those who were able to cooperate in completing the scale; and (iv) voluntarily participating in this study.

Exclusion criteria

Exclusion criteria: ? history of mental illness or congenital mental retardation; ? regular use of sleeping pills, antidepressants, anti-anxiety drugs in the past month; ? due to the use of drugs, such as antiepileptic drugs caused by cognitive impairment; ? history of pesticide, gas or alcohol poisoning, drug or alcohol dependence; ? the existence of other neurological diseases that can cause cerebral dysfunction and serious medical disease patients; ? People with hearing and vision disorders; ? People with any form of sleep disorders other than insomnia, such as sleep apnea, restless legs syndrome, etc.; ? People with important life events in the past six months; ? People who work at night, early in the morning, and people who work at heights with high awakening requirements; ? People with high-risk of falling.

Design outcomes

Primary

MeasureTime frame
cognitive function;sleep quality;Severity of insomnia;

Secondary

MeasureTime frame
GSES;ADL;GDS-15;SAS;SF-36;General Self-Efficacy Scale, GSES;PolySomnoGraphy indicators;

Countries

China

Contacts

Public ContactJunyu Zhao/ Baoying Zhang

Fujian Medical University

1053893659@qq.com+86 180 6500 5109

Outcome results

None listed

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