Recruiting soon

Multilingual Video Education for Retinal Detachment Surgery Patients

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What is being tested

Patient Education Video Intervention

Other
Who is being recruted

Eye Diseases

+ Retinal Detachment

+ Retinal Diseases

+9 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Supportive Care Study

Interventional
Study Start: January 2026
See protocol details

Summary

Principal SponsorUniversity of Toronto
Study ContactTina Felfeli, MD, PhD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 1, 2026

Actual date on which the first participant was enrolled.

This study focuses on improving education for patients who need surgery for retinal detachment, a serious eye condition that can lead to permanent vision loss if not treated promptly. The study targets individuals from diverse cultural backgrounds who might face language barriers or have different levels of understanding about health. The aim is to see if a five-minute animated video, available in 25 different languages, can better explain the condition, the surgical procedure, and the important steps patients need to follow after surgery. This is crucial because understanding these aspects can lead to better surgical outcomes and fewer complications. Participants in the study are divided into two groups. One group receives standard verbal counselling, while the other group receives both the standard counselling and the educational video in their preferred language. Researchers will evaluate how well the participants understand the information, if their anxiety levels decrease, and how well they follow post-surgery instructions. This is measured through questionnaires that assess their knowledge and feelings. The study aims to develop effective educational tools that can be used widely to enhance patient care and make sure everyone has the same opportunities for treatment success, regardless of language or literacy challenges.

Official TitleMultilingual Animated Video Education for Retinal Detachment Surgery: A Randomized Controlled Trial
Principal SponsorUniversity of Toronto
Study ContactTina Felfeli, MD, PhD
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

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

600 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Eye DiseasesRetinal DetachmentRetinal Diseases

Criteria

5 inclusion criteria required to participate
Adults ≥18 years.

Diagnosis of primary rhegmatogenous retinal detachment.

Planned repair with pneumatic retinopexy (PnR), pars plana vitrectomy (PPV), or scleral buckle (SB).

Able to provide informed consent.

Show More Criteria

4 exclusion criteria prevent from participating
Repeat retinal detachment surgery in study eye.

Combined complex procedures (e.g., PPV + corneal transplant).

Severe cognitive impairment precluding consent.

Hearing impairment preventing use of audio track (without aid).

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Standard counselling plus a 5-minute animated video in the patient's preferred language, covering diagnosis, surgical steps, and post-operative positioning. Video includes high-contrast visuals and audio narration.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

University Health Network, Toronto Western Hospital

Toronto, CanadaOpen University Health Network, Toronto Western Hospital in Google Maps
Recruiting soonOne Study Center