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A (Prospective/Pilot) Study Evaluating the Effect of Cataract Surgery on the Daily Activity Levels of Elderly Patients

Withdrawn
Conditions
Vision Disability
Cataract
Diabetes
Hypertension
Obesity
Interventions
Procedure: Cataract surgery
Registration Number
NCT04074954
Lead Sponsor
University of Pikeville
Brief Summary

To evaluate the effect of bilateral cataract surgery with intraocular lens implantation on the daily activity levels of elderly patients.

Detailed Description

Cataract formation is a natural aging process that can be influenced by environmental factors such as exposure to ultra violet light and diet. Additionally, metabolic disorders, such as diabetes can lead to an earlier development of cataracts. As cataracts develop, a patient's vision can be affected. Reduced vision can limit activities of daily living and may even reduce a patient's mobility. When this occurs, cataract surgery should be considered to help restore a patient's vision. With the obesity and diabetic epidemic, proper diet and exercise is a major health initiative to control these diseases. If a patient's mobility is reduced as a result of poor vision - their ability to achieve adequate daily physical activity may also be effected. It is thought that improvement in vision may increase their activity levels and help combat these health issues. This study will investigate the activity level of patients before and after undergoing cataract surgery to determine how improved vision quality from removal of the natural lens inside the eye and replacement with an artificial intraocular lens effects their activity level.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Patients undergoing bilateral cataract extraction by phacoemulisficatin with intraocular lens implantation and a planned bilateral distance vision target or patients with bilateral cataracts who are not having cataract surgery
  • Patients aged 60 years old or older
  • Best corrected visual acuity worse than 20/20 in each eye (meaning 20/25 or worse)
  • Non-comanged patients
Exclusion Criteria
  • Greater than 0.76 D pre-operative corneal cylinder, if having cataract surgery without a planned astigmatism correction (I.e Limbal relaxing incision or Toric intraocular lens)
  • Planned implantation of a multifocal intraocular lens
  • Visual field defect which may reduce mobility
  • Wheel chair bound patients
  • Reduced vision from an ocular disease other than cataracts
  • Patients with significant dementia who are not able to fully comprehend the informed consent

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Cataracts present, yes surgeryCataract surgeryadult patients who have cataracts but are not undergoing cataract surgery
Primary Outcome Measures
NameTimeMethod
Amount of activity conducted by the patient after receiving surgery10 days after surgery

Measured by a wrist activity tracker

Amount of activity conducted by the patient before receiving surgery10 days prior to surgery

Measured by a wrist activity tracker

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Bennett and Bloom Eye Centers

🇺🇸

Louisville, Kentucky, United States

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