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Effect of an Educational Program on Health-related Outcomes of Patients With Dry Eye Syndrome

A

Alexandria University

Status

Completed

Conditions

Dry Eye Syndrome

Treatments

Other: Educational Program

Study type

Interventional

Funder types

Other

Identifiers

NCT06288945
Dry eye syndrome

Details and patient eligibility

About

Dry eye syndrome (DES) is a widespread ocular disease affecting the general population. It is a complex disorder affecting the surface of the eye, marked by an imbalance in the tear film and ocular symptoms. Therefore this study was done to determine the effect of an educational program on health-related outcomes of patients with DES including the severity of symptoms related to DES and their influence on visual-related functions

Full description

Dry eye syndrome (DES) is a prevalent chronic, inflammation resulting in eye discomfort, irritation, tiredness, and visual abnormalities that can make it difficult to read, use a computer, drive, or engage in other activities (1). It represents a set of tears film disorders caused by decreased tears formation or increased tears evaporation; it causes visual symptoms, ocular surface inflammation, and discomfort. In addition, DES leads to impaired visual function and can negatively affect the outcomes of cataract surgery (2).Therefore this study was done to determine the effect of an educational program on health-related outcomes of patients with DES including the severity of symptoms related to DES and their influence on visual-related functions

Enrollment

60 patients

Sex

All

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age: 20 to 60 years old.
  • Alert, and able to communicate.

Exclusion criteria

  • patients with recent ocular surgeries in the last 3 months

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Study Group
Experimental group
Description:
The educational nursing interventions were individually administered to each participant in the study group in two sessions which were conducted after the assessment phase on the day of the eye examination at the ophthalmology outpatient clinic and after the diagnosis of dry eye syndrome.
Treatment:
Other: Educational Program
Control Group
No Intervention group
Description:
The control group was selected first and did not receive the educational program for dry eye syndrome

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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