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Cognitive function in perimenopausal women based on fNIRS and ApoE gene polymorphisms

Cognitive function in perimenopausal women based on fNIRS and ApoE gene polymorphisms

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081543
Enrollment
Unknown
Registered
2024-03-05
Start date
2024-03-10
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Cognitive Impairment

Interventions

Sponsors

The People's Hospital of Bao'an, Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1 Perimenopausal women without cognitive impairment: (1) Meet diagnostic criteria for perimenopause; (2) Are between 40-60 years of age; (4) Satisfy an SCD-Q9 score of <5; (5) Satisfy a MoCA score of =26; (if =12 years of education, add 1 point to the score) (6) Right sharp hand; (7) Signed informed consent and voluntary participation. 2 .SCD perimenopausal women: (1) Meet the diagnostic criteria for SCD; (2) Meet perimenopausal diagnostic criteria; (3) Aged between 40-60 years old; (4) Satisfy SCD-Q9 score =5; (5) Satisfaction of a MoCA score of =26; (if =12 years of education, add 1 point to the score) (6) Right sharp hand; (7) Signed informed consent and voluntary participation. 3. MCI perimenopausal women: (1) Meet MCI diagnostic criteria (2) Meet perimenopausal diagnostic criteria: (3) Are between 40-60 years of age; (4) Satisfy a MoCA score of between 18-25; (if =12 years of education, add 1 point to the score) (5) Right sharp hand; (6) Signed informed consent to participate voluntarily.

Exclusion criteria

Exclusion criteria: (1) A history of mental illness; (2) A history of neurological disorders; (3) History of alcohol or drug abuse; (4) Surgical menopause (history of hysterectomy and bilateral adnexa removal); (5) Tumors of the reproductive system and vaginal bleeding of unknown etiology; (6) Hormonal drugs in the last 3 months prior to participation in the study; (7) Those who are unable to complete the assessment of indicators, such as severe aphasia, deafblindness, illiteracy, etc; (8) Participating in other research trials that affect the results of this study; (9) Not signing the informed consent.

Design outcomes

Primary

MeasureTime frame
Subjective Cognitive Decline Questionnaire9 (SCD-Q9);Montreal Cognitive Assessment Scale (MoCA Scale);N-back mission;

Secondary

MeasureTime frame
ApoE gene polymorphism detection;Menopause Rating Scale (MRS);Self-rating Scale for Anxiety (SDS);Depression Screening Scale (PHQ);Pittsburgh Sleep Quality Index (PSQI);

Countries

China

Contacts

Public ContactChen Shangjie

The People's Hospital of Bao'an, Shenzhen

Csjme@163.com+86 158 9979 7851

Outcome results

None listed

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