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NCT Number: NCT07715695

Evaluation of a Scalable Educational Intervention for Adjustment and Coping to Vision Loss

The goal of this interventional study is to learn if an educational intervention improves awareness in people experiencing visual loss. The main question it aim to answer is:

* Will participants have an improved awareness of shared experiences regarding themes such as grief and isolation?

Participants will be asked to answer questions, engage with an audiovisual educational intervention, and then answer additional questions.

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Key information

Conditions

Visual Loss Eye Diseases Nervous System Diseases Neurologic Manifestations Pathological Conditions, Signs and Symptoms Sensation Disorders Signs and Symptoms Vision Disorders

Age range

18 year–89 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Brigham and Women's Hospital, Mass General Brigham, Boston, Massachusetts, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • have capacity to provide informed consent
  • have had a visit within a low-vision rehabilitation clinic

Exclusion criteria

  • are unable to engage with the audiovisual educational intervention

Treatment and study plan

audiovisual educational intervention

Other

A brief audiovisual educational intervention.

Primary outcomes

  1. Change from Baseline in Educational Awareness of Shared Themes as Measured by Likert-scale Questions

    Time frame: From baseline to completion of post-intervention questions (e.g., within 1 week).

    Higher values (or increases relative to baseline) correspond to better outcomes, with each question having a minimum value of 1 and a maximum value of 5.

Secondary outcomes

  1. Change from Baseline in Screening Measures of Depression and Anxiety as Measured by the Patient Health Questionnaire 4 (PHQ-4)

    Time frame: From baseline to completion of post-intervention questions (e.g., within 1 week).

    Lower values (or decreases relative to baseline) correspond to better outcomes, with each question having a minimum value of 0 and a maximum value of 3.

  2. Change from Baseline of Vision-Related Wellbeing as Measured by the Visual Function Questionnaire 25 (VFQ-25) Socioemotional Wellbeing Subscale

    Time frame: From baseline to completion of post-intervention questions (e.g., within 1 week).

Study contacts

Contact information is provided by the study sponsor or research team.

Research Coordinator

CONTACT

[email protected]

617-732-6753

Sponsors and collaborators

Lead sponsor

Brigham and Women's Hospital

Other

Collaborators

  • Hadley Foundation, Inc.
  • New England College of Optometry

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 20, 2026
Registry last updated
Jul 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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