Evaluation of the Effect of Cataract Surgery on Cognitive Function in Very Elderly Patients

August 5, 2019 updated by: Gian Maria Cavallini, University of Modena and Reggio Emilia

The study intends to measure the evolution over time of the cognitive capacity of patients undergoing cataract surgery in relation to the opaque lens removal surgery (cataract) in a population considered to be at risk of neurocognitive degeneration.

Secondary objectives:

• Estimate the incidence of postoperative cognitive dysfunctions and any episodes of perioperative delirium with the aim of demonstrating the safety of cataract surgery in the elderly patient in terms of cognitive functions and impact on the psychological state.

In the context of the study a risk sub-population analysis will be carried out, evaluating the trend over time of the "endothelial cells count" parameter

The elderly population remains, due to the aging of the cornea, a population "at risk" for significant alterations from the clinical point of view. During the study the endothelial cells count will be monitored, in order to be able to evaluate the safety of the cataract surgery and to be able to correctly correlate a possible deterioration in the visual acuity of patients with corneal decompensation. To evaluate the progress of the endothelial cells count in the elderly patient during the pre-intervention and post-intervention period. Since the low values of cellular media in endothelial microscopy are an element that increases the risk of complications during cataract surgery, the study wants to assess how waiting times between filter visits and cataract surgery can cause an elderly patient worsening of this parameter even in a few months. The trend of the same parameter will be monitored even after the intervention since in case of decrease, the low endothelial count could cause an alteration of visual acuity and therefore a minor improvement in cognitive performance.

The research will be set as a longitudinal observational study where will be compared in each patient the parameters analyzed in the 6 months prior to cataract surgery and in the 3 months following the operation itself. Patients will be enrolled during the first cataract filter visit, will be submitted to simple questions and their clinical data will be collected. Subsequently, before and after three months of surgery repeated cognitive testing and the control normally performed instrumental tests during follow-up.

A clinical follow-up will be provided, during normal follow-up visits at 20 days and 6 months after the patient's surgery: the following information will be collected during these visits

  • BCVA (visual acuity)
  • endothelial cells microscopy
  • OCT macula and optic nerve
  • Catquest 9SF;
  • Barthel Index;
  • Six Item Cognitive Test
  • Confusion Assessment Method (CAM): this exam will be performed within 24 hours of post-surgery and 20 days after surgery.

It is important to underline that the cognitive tests proposed to patients consist of simple questions that do not depend on the visual ability of the subject.

Study Overview

Detailed Description

Study design: prospective, monocentric, epidemiological study: non-interventional. The drafting of the protocol follows the order proposed by the STROBE check-list for the publication of the observational studies where applicable.

There is no agreement between promoter and clinical center.

There is no agreement between promoter and financier: the study has no funding. The study is also carried out for the purpose of completing a thesis.

Rational

The constant aging of the population in western countries has led to an increase in the incidence of visual deficits in the elderly, the incidence of cataract is around 68%, at the same time this category of subjects frequently has cognitive deficits that can be minimal or severe as in the case of dementias.

The individual's visual capacity is correlated with the neurological progression of these morbid states. Numerous studies have long sought a correlation between sensory (visual and auditory) functionality and cognitive faculties in old age, defining how sensory functions can be considered indicators of the integrity of the central nervous system.

Further studies, always focused on this current research, focused on a correlation between the improvement of visual acuity through the IOL (Intra Ocular Lens) implant and the improvement of cognitive faculties. Further studies have focused their attention not only on cognitive faculties, but on the psychological aspect in terms of improving the quality of life following cataract surgery. Simultaneously, Cataract surgery has been referred as one the most effective healthcare intervention to prevent and lower the risk of falls, hips and lower limbs fracture, trauma and social isolation.

The improvement of the visual capacity, the cognitive faculties and the psychological state of the elderly patient are certainly useful elements for improving the quality of life of the subject but also for the caregiving burden on the elderly patient by the caregivers and the NHS. A 1998 study found a strong association between visual impairment (caused by altered contrast sensitivity, reduced field of vision and the presence of cataracts) and the increase in falls in the elderly.

Materials and methods

Patients will be enrolled during the filter visits of the ophthalmology clinic: whenever the need for replacement of the operative lens will be diagnosed, the patient will be offered to participate in the data collection by providing the information sheet. Subsequently consent will be collected. Data collection will be undertaken when the consent is signed. An identification code will be assigned exclusively to each patient. The patient's personal data will be entered through the creation of the Patient's list, to keep personal data confidential.

In no case will experimental treatments be provided to the patient: the study includes a collection of clinical information already normally collected during preoperative visits, outpatient visits and during follow-up checks.

The research will be set as a longitudinal observational study where will be compared in each patient the parameters analyzed in the 6 months prior to the cataract operation and in the 3 months following the operation itself.

The cognitive state will be measured over time: during enrollment, on the day of surgery, 20 days after surgery and 3 months after surgery.

Patients will be enrolled during the first cataract filter visit, will be submitted to simple questions and their clinical data will be collected.

A comparison will also be made in terms of incidence of neuro-cognitive and delirium problems in relation to the patient's age and cataract surgery. The great elderly population has a higher risk to encounter a momentaneous cognitive disfunction, due to psycological and physical stress induced by surgery and anesthesia. This study, considering this important element, will indirectly estimate the safety of cataract surgery. The post-operative delirium incidence in a surgical ward is considered an important parameter of quality of care in terms of patient's care and technical management in the ward.

The information sheet will be provided during the filter visit for the insertion of the patient on the waiting list for cataract surgery and consent will be collected after this.

The following parameters will be analyzed: demographic variables, level of education, presence of relatives during the visit, patient history of proximal and remote patient, home therapies, performed analyzes of practice during outpatient visits: BCVA visual acuity (ETDRS optotype tables), microscopy endothelial, OCT macula and optic nerve to exclude the presence of a maculopathy and a deficit of nerve fibers such as to affect the improvement of visual and cognitive function.

Following the collection of the consent, questionnaires will be provided to the patients enrolled to measure the functional cognitive capacity of the subject such as:

Quality of life, Catquest 9SF. The Catquest evaluation consists of 9 questions, evaluating the perceived quality of vision in routine activities like reading, shopping, recognizing individuals or doing recreational activities. The 9 questions present a speicific scale of 5 measures, from "Great Difficult" to "No difficult". The rationale beneath this test is to evaluate the ratio between the personal perception of visual function before and after surgery, evaluating in parallel trends of the mean of the scores calculated. A comparison will be also set between eleders and great elders, to evaluate eventual differences between the perceived result of surgery and the real visual acuity.

Scale of evaluation of daily life activity, Barthel Index. Many clinical studies associated the surgical removal of opacified lens with an increase of independence, due to the increase of visual function. To measure eventual changes, the Barthel Index has been chosen and added inside the protocol. The Barthel scale is an ordinal scale used to measure performance in activities of daily living (ADL). Each performance item is rated on this scale with a given number of points assigned to each level or ranking. This test is used by general physicians, physiotherapists, neurologists and rehabilitation nurses to calculate the trend of physical independence of an individual. This Index evaluates the physical necessities in daily activities like personal hygiene, Mobility, feeding, dressing, bladder control and bowels. The evaluation in this case consists on a score between 0-100 where 100 means complete independence and 0 absolute dependence on someone else.

Cognitive state measured with the Six Item Cognitive Impairment Test (6CIT). Number of questions: 6. Time taken to perform: 3-4 minutes. Score: the 6CIT uses an inverse score and questions are weighted to produce a total out of 28. Scores of 0-7 are considered normal and 8 or more significant. Advantages: the test has high sensitivity without compromising specificity, even in mild dementia. It is easy to translate linguistically and culturally. Disadvantages: the main disadvantage is in the scoring and weighting of the test, which is initially confusing; however, computer models have simplified this greatly.

Probability statistics: at the 7/8 cut-off: Overall figures - sensitivity = 90%, specificity = 100%; in mild dementia, sensitivity = 78%, specificity = 100%. Differently from older studies, the choice of this evaluation method The quickness of the administration of the test and more importantly, the exclusive use of question, and not the use of visual function provides to the study a more complete and purified view of the cognitive function, configuring this study as a innovation in the field.

Following the secondary outcomes, the corneal behavior will be measured between the different groups, focusing on the age criteria. Considering a physiological lowering of the quality of the cornea, the phacoemulsification is a physical stress for the ocular structure, raising the risk of corneal decompensation. To tangibly measure the corneal behavior, corneal thickness and corneal endothelial cells density have been chosen as main parameters. The CSO Perseus 400 (Florence - IT) will be used to study corneal behavior.

At the same time, the Optical Coherence Tomography will be used to evaluate the Macula and the optical nerve modifications after cataract surgery. This evaluation will be set in the highest risk period (up to 30 days after cataract surgery). The Irvine Gass macular edema and optical nerve insults can be a cause of lower visual improvement after a correct cataract surgery. The OPKO OCT/SLO will be used to conduct these measures.

Study Phases and Times

Time 0: patient enrollment (on average 4 months before surgery) Time 1: perioperative time Time 2: check at 20 days Time 3: check at 3 months

It is important to underline that the cognitive tests proposed to patients consist of simple questions that do not depend on the visual ability of the subject.

Finally, the study will compare the incidence data of neuro-cognitive problems in those who have undergone surgery in relation to the patient's age group and cataract surgery.

Data are analyzed using the R-Software, and using the ANOVA calculation method. Analysis of variance (ANOVA) is a collection of statistical models and their associated estimation procedures (such as the "variation" among and between groups) used to analyze the differences among group means in a sample. With this analysis, the trend of each variable will be analyzed.

Study Type

Observational

Enrollment (Anticipated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Modena, Italy, 41124
        • Policlinico di Modena

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years and older (OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The studied population consists in people who can really obtain a visual acuity recovery with cataract surgery. All the variables are measured in a very elderly population (high risk population) and compared them in a elderly population (lower risk)

Description

Inclusion Criteria:

  • Patients with age ≥ 65 years undergoing cataract surgery. Cataract surgery is indicated by the medical-scientific community according to good clinical practice and not influenced by the study's criteria. The purpose of the study is to add clinical-scientific information of any relevance.

Exclusion Criteria:

  • Patient refusal
  • Diagnosis of dementia by the specialist in neurocognitive diseases (neurologist and / or geriatrician)
  • maculopaties and other ophthalmopaties (according to diagnosis of ophthalmologist specialist) because the visual capacity is invalidated regardless of the opacification of the crystalline and therefore the cognitive function is not affected by a post-intervention improvement.
  • Patients who have performed cataract surgery in at least one eye since the previous cataract operation may have already caused changes in cognitive function causing confusion about the results of the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Elderly Female (A)
Female subjects between 65 and 85 years old
During T0, T2 and T3, every subject has been evaluated with a Snellen Chart, to measure visual acuity in number of letters (BVCA)
During the first 48 hours of post-op follow-up, any episode of "post-operative Delirium" is checked and evaluated.
The questionnaire contains questions evaluating the benefits of cataract surgery. The questionnaire has been used during T0, T2 and T3
Using the RNFL and the Macular Topography protocol, the macula and optical nerve are measured during the T2 phase of each patient the risk of Irvine Gas's syndrome or any other retinal complication.
Other Names:
  • Optical Coherence Tomography
This Cognitive Impairment test doesn't require Visual function to be executed. Cognitive function is evaluated at T0, T1 and the post-operative trend at T2 and T3.
Other Names:
  • Kingship Test
To evaluate the everyday independence of the subject and it's trend durin the follow-up
Endothelial cell density is evaluated before surgery (T0) and during the follow-up (T2 and T3). The reason of the choice of this test is to evaluate the trend of these instrumental parameters in the elderly population.
Great Elderly Female (B)
Female subjects with more than 85 years old
During T0, T2 and T3, every subject has been evaluated with a Snellen Chart, to measure visual acuity in number of letters (BVCA)
During the first 48 hours of post-op follow-up, any episode of "post-operative Delirium" is checked and evaluated.
The questionnaire contains questions evaluating the benefits of cataract surgery. The questionnaire has been used during T0, T2 and T3
Using the RNFL and the Macular Topography protocol, the macula and optical nerve are measured during the T2 phase of each patient the risk of Irvine Gas's syndrome or any other retinal complication.
Other Names:
  • Optical Coherence Tomography
This Cognitive Impairment test doesn't require Visual function to be executed. Cognitive function is evaluated at T0, T1 and the post-operative trend at T2 and T3.
Other Names:
  • Kingship Test
To evaluate the everyday independence of the subject and it's trend durin the follow-up
Endothelial cell density is evaluated before surgery (T0) and during the follow-up (T2 and T3). The reason of the choice of this test is to evaluate the trend of these instrumental parameters in the elderly population.
Elderly Male (C)
Male subjects between 65 and 81 years old
During T0, T2 and T3, every subject has been evaluated with a Snellen Chart, to measure visual acuity in number of letters (BVCA)
During the first 48 hours of post-op follow-up, any episode of "post-operative Delirium" is checked and evaluated.
The questionnaire contains questions evaluating the benefits of cataract surgery. The questionnaire has been used during T0, T2 and T3
Using the RNFL and the Macular Topography protocol, the macula and optical nerve are measured during the T2 phase of each patient the risk of Irvine Gas's syndrome or any other retinal complication.
Other Names:
  • Optical Coherence Tomography
This Cognitive Impairment test doesn't require Visual function to be executed. Cognitive function is evaluated at T0, T1 and the post-operative trend at T2 and T3.
Other Names:
  • Kingship Test
To evaluate the everyday independence of the subject and it's trend durin the follow-up
Endothelial cell density is evaluated before surgery (T0) and during the follow-up (T2 and T3). The reason of the choice of this test is to evaluate the trend of these instrumental parameters in the elderly population.
Great Elderly Male (D)
Men subjects with more than 81 years old
During T0, T2 and T3, every subject has been evaluated with a Snellen Chart, to measure visual acuity in number of letters (BVCA)
During the first 48 hours of post-op follow-up, any episode of "post-operative Delirium" is checked and evaluated.
The questionnaire contains questions evaluating the benefits of cataract surgery. The questionnaire has been used during T0, T2 and T3
Using the RNFL and the Macular Topography protocol, the macula and optical nerve are measured during the T2 phase of each patient the risk of Irvine Gas's syndrome or any other retinal complication.
Other Names:
  • Optical Coherence Tomography
This Cognitive Impairment test doesn't require Visual function to be executed. Cognitive function is evaluated at T0, T1 and the post-operative trend at T2 and T3.
Other Names:
  • Kingship Test
To evaluate the everyday independence of the subject and it's trend durin the follow-up
Endothelial cell density is evaluated before surgery (T0) and during the follow-up (T2 and T3). The reason of the choice of this test is to evaluate the trend of these instrumental parameters in the elderly population.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Correlation between visual acuity and cognitive function at 3 months after Cataract Surgery.
Time Frame: 6 months before surgery to 3 months after surgey

The visual acuity trend and the cognitive function using the Kingshill (6CIT) score are measured during every visit. The 6 Item Cognitive Impairment Test (6CIT) is a test that doesn't provide the visual function. The choice of this kind of test resides in the capability of evaluating the cognitive function without any influence caused by cataract. The score is composed by 6 questions which evaluate the work memory, the temporal and spatial orientation. The test's result is a score, with a clinical cut-off of 7 points. The more points the subject makes, the higher risk of cognitive impairment is configured.

The visual acuity is calculated with Snellen Chart using the Best Corrected Visual Acuity (BCVA) with the number of letters read.

6 months before surgery to 3 months after surgey

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Post operative delirium prevalence
Time Frame: Only during the perioperative period (day of cataract surgery and the next 48 hours)
The prevalence of post operative delirium is measured using the Confusion Assessment Method Evaluation.
Only during the perioperative period (day of cataract surgery and the next 48 hours)
Corneal endothelial cells density
Time Frame: 6 months before surgery, 20 days after cataract surgery and 3 months after cataract surgery.
Thanks to the Endothelial Microscopy Evaluation, the corneal performance will be measured in terms of density of endothelial cells
6 months before surgery, 20 days after cataract surgery and 3 months after cataract surgery.
Corneal pachymetry
Time Frame: 6 months before surgery, 20 days after cataract surgery and 3 months after cataract surgery.
Thanks to the Corneal Pachymetry, the corneal performance will be measured in terms of density of corneal thickness.
6 months before surgery, 20 days after cataract surgery and 3 months after cataract surgery.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gian Maria Cavallini, Associate Professor, Dipartimento Chirurgico, Medico, Odontoiatrico e di Scienze Morfologiche con interesse Trapiantologico, Oncologico e di Medicina Rigenerativa - UNIMORE - University of Modena and Reggio Emilia

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

February 2, 2019

Primary Completion (ANTICIPATED)

February 28, 2020

Study Completion (ANTICIPATED)

March 30, 2020

Study Registration Dates

First Submitted

July 25, 2019

First Submitted That Met QC Criteria

August 5, 2019

First Posted (ACTUAL)

August 6, 2019

Study Record Updates

Last Update Posted (ACTUAL)

August 6, 2019

Last Update Submitted That Met QC Criteria

August 5, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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