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Effects of cataract and idiopathic macular epiretinal membrane on patients' emotional and cognitive function

Effects of cataract and idiopathic macular epiretinal membrane on patients' emotional and cognitive function

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081443
Enrollment
Unknown
Registered
2024-03-01
Start date
2024-03-04
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

cataract and idiopathic macular epiretinal membrane

Interventions

Cataract Group:NA
IMEM Group:NA

Sponsors

The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan Province, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 120 Years

Inclusion criteria

Inclusion criteria: Criteria for inclusion in the cataract group: 1. Patients who visited our ophthalmology department and were diagnosed with cataracts. 2. Age = 65 years old. 3. Willing to participate in this study by signing an informed consent form. Criteria for inclusion in the IMEM group: 1. Patients who visited our ophthalmology department and were diagnosed with IMEM. 2. Age = 65 years old. 3. Willing to participate in this study by signing an informed consent form. Criteria for inclusion in the healthy control group: 1. Participants who underwent health examinations at our hospital's health examination center during the same period and have no ophthalmic diseases. 2. Age = 65 years old. 3. Willing to participate in this study by signing an informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. History of anxiety, depression, mild cognitive impairment, or dementia. 2. Severe visual or hearing impairment, or physical disabilities that prevent completion of questionnaire surveys. 3. Currently participating in other clinical studies. 4. Exhibiting violent tendencies that may endanger the safety of others. 5. Presence of other severe chronic systemic diseases. 6. Experiencing significant life events in the three months prior to study participation. 7. Previous intraocular lens implantation surgery. 8. Conditions or diseases deemed by the researchers to potentially affect protocol compliance or deemed unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Cognitive Status Assessment;Depression;Anxiety;

Secondary

MeasureTime frame
Sleep status;Quality of daily life;Changes in brain function and neural networks before and after surgery;Differences in brain function and neural networks between cataract patients and healthy individuals;Differences in brain function and neural networks between cataract patients and healthy individuals;Changes in best corrected visual acuity before and after cataract surgery in patients;

Countries

China

Contacts

Public ContactXiaolei Liu

The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan Province, China

ringlxl@163.com+86 138 8881 2292

Outcome results

None listed

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