Evaluating visual rehabilitation's effects on anxiety and depression in patients with AMD

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the impact of a visual rehabilitation program on anxiety and depression levels in visually impaired patients suffering from advanced age-related macular degeneration (AMD). Participants will undergo a series of assessments, including ophthalmological examinations and questionnaires measuring anxiety and depression. The study involves three visits: an initial screening, a 60-day rehabilitation program with group meetings, and a final evaluation to measure outcomes. The research is conducted at two locations in Rome, Italy.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Subjects ≥ 55 years
2. Moderate and severe visual impairment (BCVA ≥1/10 and ≤2/10)
3. Diagnosis of advanced non-exudative age-related macular degeneration (AMD)
4. Informed consent freely granted and acquired before the start of the study
5. Ability to understand and willingness to follow the study instructions and procedures

Exclusion Criteria:

1. Visual impairment due to other ocular diseases
2. Mild visual impairment or partial or total blindness
3. Exudative age-related macular degeneration undergoing intravitreal drug treatment

Where it's running

• IRCCS Fondazione G.B.Bietti
  Rome, Italy, Italy Recruiting

Study contacts

• Study coordinator: Eliana Costanzo, MD
• Email: eliana.costanzo@fondazionebietti.it
• Phone: +390684009442

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.