Reduced ER-QOL in Families After Congenital Cataract Surgery

A Prospective Study on Assessments of the Eye-related Quality of Life, Functional Vision, and Their Determinants Using the PedEyeQ in Children After Congenital Cataract Surgery and Their Families

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04824755

Enrollment

166

Registered

2021-04-01

Start date

2020-07-01

Completion date

2021-01-01

Last updated

2021-04-01

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

Conditions

Prospective Cross-sectional Study

Brief summary

Children after congenital cataract surgery experience a lower quality of life and reduced functional vision. Their families have also been seriously affected. Investigators should pay more attention to them, and measures should be administered to families.

Interventions

PROCEDUREYune Zhao

Yune Zhao did congenital cataract surgeries

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

0 Years to 11 Years

Healthy volunteers

Yes

Inclusion criteria

* visually not significant cataract, and ophthalmic surgery (incisional or laser) within one month

Exclusion criteria

* parents who were inability to communicate were also excluded

Design outcomes

Primary

Measure	Time frame	Description
Gender of Child	through study completion, an average of half a year	female,male
Parent/legal guardian Age	through study completion, an average of half a year	under 25,26-30,31-35,36-40,over 41
Parent/legal guardian completing questionnaires	through study completion, an average of half a year	father,mother,legal guardian
Native Place	through study completion, an average of half a year	city,not the city
Parent/legal guardian highest level of education	through study completion, an average of half a year	Primary school graduate,Junior-high graduate/technology secondary school graduate,high school graduate/junior college degree,College graduate,Postgraduate/professional degree
Staging operation	through study completion, an average of half a year	primary IOL implantation, aphakia, secondary IOL implantation;using questionnaire and telephone follow-up
Postoperative timing	through study completion, an average of half a year	Less than 1 year,1 to 2 years,2 to 3 years,More than 3 years;using questionnaire and telephone follow-up
Amblyopia treatment	through study completion, an average of half a year	Cooperative,Average,Uncooperative,No treatment;using questionnaire and telephone follow-up

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026