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Phase 3 N=241 Randomized Single-blind Treatment

Improving Function in Age-Related Macular Degeneration

Age-Related Macular Degeneration

Enrolled (actual)
241
Serious AEs
26.6%
Results posted
Oct 2015
Primary outcome: Primary: Targeted Vision Function (TVF) — 2.18; 2.14 units on a scale — p=.47

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
PST (Behavioral); ST (Behavioral)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
Thomas Jefferson University
Primary completion
Jun 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Targeted Vision Function (TVF)
2.18; 2.14 .47
PRIMARY
Targeted Vision Function
2.18; 2.15
SECONDARY
Vision-related Quality of Life
66.4; 64.8
SECONDARY
Vision-related Quality of Life
66.4; 64.8

Summary

This randomized, controlled clinical trial will test the efficacy of Problem-Solving Treatment (PST) to improve vision function in older persons with age-related macular degeneration (AMD). AMD is a highly prevalent, disabling disease of aging that causes severe vision loss and functional decline. It is the leading cause of blindness in older persons in the United States and may affect more than 10 million people. Currently, there are no effective treatments to restore vision. Thus, improving Vision Function is a major goal of treatment. Vision function refers to vision-related abilities to perform daily living activities (e.g. reading recipes to prepare meals). Decrements in vision function will become a major public health problem as the population ages and the prevalence of AMD increases. PST is a brief, standardized, cognitive-behavioral treatment that teaches problem-solving skills. We believe PST will enable patients with AMD find practical solutions to vision-related problems and thereby improve vision function. We will recruit 240 AMD patients from the retina clinics of Wills Eye Institute, Philadelphia, PA, with bilateral AMD and visual acuity worse than 20/70 in the better eye. PST-trained therapists will deliver 6 1-hour, in-home sessions to the 120 subjects randomized to PST. The control treatment is Supportive Therapy (ST), a similarly structured, standardized psychological treatment that controls for the non-specific effects of treatment (n=120). ST contains no active elements beyond its non-specific components; in this way it is a placebo treatment. Independent raters, masked to treatment assignment, will assess Targeted Vision Function (primary outcome) and vision-related quality of life (secondary outcome) at 3 months to assess PST's efficacy, and at 6 months to evaluate its long-term effects. As the population ages, the disability of AMD will become more prevalent, costly, and burdensome to patients, families, and ophthalmologists. This makes devising and testing practical and affordable interventions to improve vision function a national priority.

Eligibility Criteria

Inclusion Criteria

  • Being at least 65 years old
  • Having bilateral Age-Related Macular Degeneration (AMD) (atrophic or neovascular)
  • Having a best corrected visual acuity of 20/70 or worse
  • Moderate difficulty in at least one valued vision functional goal

Exclusion Criteria

  • Ophthalmologic Criteria. Patients who have uncontrolled glaucoma (continued visual field loss and increase in optic nerve cupping), diabetic retinopathy (due to macular edema), or cataracts for which surgery within 6 months is likely will not be eligible to participate. This information will be obtained from patients' ophthalmology charts and discussion with the patient's ophthalmologist.
  • Cognitive Impairment Criteria. Cognitive functioning will be evaluated by the Project Director during the telephone screen (see Chapter 9). Patients with cognitive impairment will not be eligible to participate.
  • Health Criteria. Patients with life-threatening illness (e.g., terminal cancer, need for oxygen) will not be eligible to participate. Information regarding heath status will be gleaned from patient's ophthalmology charts.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00572039). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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