Problem Solving Training and Low Vision Rehabilitation
Completed · Not applicable · Has a placebo group
Conditions studied: Low Vision
In brief
Vision loss can result in feelings of frustration, helplessness, anxiety, depression, and anger, which compromise a person's activities of everyday living. While emotional distress may resolve in some persons without intervention, unmanaged and persistent distress places the person at risk for continued decrements in health status and the potential development of more severe conditions (i.e., depression, poor health outcomes). Persons with low vision will be recruited and randomly assigned to either an innovative, problem-solving training (PST) intervention group designed specifically for persons with low vision or a sham intervention/control group. Primary and secondary outcomes will be assessed at baseline prior to intervention and at 3 month follow-up, 7 month follow-up, 12 month follow-up, and 24 month follow-up by a research interviewer masked to participants' randomization. This project will: (1) demonstrate how specified physical and emotional outcomes of persons with low vision change across time, (2) evaluate the effectiveness of a PST intervention that will be delivered to persons with low vision; and (3) identify persons with low vision who are at risk for adverse emotional and health outcomes.
Key facts
- Study ID
- NCT00545220
- Run by
- University of Alabama at Birmingham
- People needed
- 430
- Starts
- 2007-10-01
- Expected to finish
- 2015-12-01
- Last updated by the study team
- 2016-02-19
Who can join
Age: 19 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- +19 yrs of age
- Underwent a low vision rehabilitation initial eye exam
- No more than 2 errors on cognitive on cognitive screening measure (SPBS)
- Must have access to telephone
- No significant hearing problems
- No significant communication problems
- Speaks fluent English
Where it is running
- University of Alabama at Birmingham — Birmingham, Alabama, United States
Full record on ClinicalTrials.gov
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