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Study identifier: NCT06906003 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Visual Rehabilitation and Depression in Visually Impaired Patients With AMD

Condition: AMD - Age-Related Macular Degeneration · Anxiety · Depression Disorders  ·  Sponsor: Fondazione G.B. Bietti, IRCCS

PhaseN/A
Planned participants22
Who can joinAll sexes, 55 Years to no upper limit
Healthy volunteersNo

About this study

Purpose: The aim of this study is to evaluate the impact of visual rehabilitation in visually impaired patients with advanced AMD by the use of questionnaires on the anxiety and depression status. Study design: prospective observational study. The study is carried out at the IRCCS Fondazione G.B.Bietti and at the UO Visual Rehabilitation, S. Alessio - Margherita di Savoia. Study procedures: Visit 1 (screening visit, at IRCCS Fondazione Bietti) After signing the informed consent, all patients received a complete ophthalmological examination, non-invasive diagnostic tests as optical coherence tomography, autofluorescence and microperimetry, and have to complete the questionnaires on the state of anxiety and depression (GAD-7 and PHQ-9). Visit 2 (at the Sant'Alessio Institute) for a 60-day visual rehabilitation program scheduled in 5 group meetings. Visit 3 (end-of-study visit, at IRCCS Fondazione G.B. Bietti) complete ophthalmological examination, as per clinical practice, non-invasive diagnostic tests such as microperimetry, optical coherence tomography and autofluorescence and administration of the Patient Health Questionnaire-9 (PHQ-9) questionnaires for depression and the General Anxiety Disorder (GAD-7) questionnaires for anxiety.

This description comes directly from the study's public registry record.

Talk to the study team

Eliana Costanzo, MD  ·  +390684009442  ·  eliana.costanzo@fondazionebietti.it

Always discuss trial participation with your own doctor first.

Locations (1)

IRCCS Fondazione G.B.BiettiRome, Italy, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06906003