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Effect of Mobile Communication on Congenital Ectopia Lentis Follow-up Adherence

Sun Yat-sen University logo

Sun Yat-sen University

Status

Active, not recruiting

Conditions

Ectopia Lentis

Treatments

Other: smartphone application service and phone reminder

Study type

Interventional

Funder types

Other

Identifiers

NCT05628129
IIT2022120

Details and patient eligibility

About

Regular follow-up is essential to successful management of congenital ectopia lentis, but it is often ignored by parents in China.

With rapid economic development, there are increasing numbers of mobile phone users that allow for communication applications to be used in medical care.

The investigators aimed to assess the potential of the smartphone application assisted medical service to increase patient compliance in attendance of follow-up after congenital ectopia lentis treatment.

Full description

Congenital ectopia lentis is a rare ophthalmic disease that seriously harms the physical and mental health of patients. Surgery is the only definite treatment at present. However, severe visual impairment is common in congenital ectopia lentis patients in China, and delayed presentation to hospital and late surgical treatment are found to be the major reasons.

In China, the messaging application WeChat has become the most popular communication tool. As most congenital ectopia lentis patients' parents are younger people, they are more likely to use technology, such as WeChat, in their daily lives. In addition, it allows ophthalmologists to utilize this communication application to relay health related information and reminders to patients. This makes it feasible to apply this smartphone application in improving attendance of follow-up visits.

In this trial, the investigators aimed to assess the potential of the smartphone application assisted medical service to increase patient compliance in attendance of follow-up after congenital ectopia lentis treatment.

Enrollment

110 patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

    1. Identified with congenital lens dislocation after surgery and age ≤ 18 years old; 2. Parents were able to access a mobile phone and communicate via the smartphone application (WeChat); 3. Agree to participate in this study and sign the informed consent.

Exclusion criteria

    1. With Other ophthalmic diseases such as glaucoma, uveitis and corneal disease.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

110 participants in 2 patient groups

reminder intervention
Experimental group
Description:
On the basis of standard appointment, parents in intervention group will receive phone reminders at 4 days and 1 day before their scheduled appointments, and relevant scientific and educational knowledge will be relayed to them from the smartphone application at 1 week before appointments.
Treatment:
Other: smartphone application service and phone reminder
standard appointment
No Intervention group
Description:
Patients will be required to attend follow-up appointments at 1 week, 1 month, 3 months after surgery.

Trial contacts and locations

1

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Central trial contact

Danying Zheng, M.D

Data sourced from clinicaltrials.gov

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