Trial record 1 of 31 for:    Open Studies | "Vision, Low"
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Problem Solving Training and Low Vision Rehabilitation

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2007 by National Eye Institute (NEI).
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Information provided by:
National Eye Institute (NEI)
ClinicalTrials.gov Identifier:
NCT00545220
First received: September 21, 2007
Last updated: October 16, 2007
Last verified: October 2007
  Purpose

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.


Condition Intervention
Low Vision
Behavioral: problem-solving training
Behavioral: sham intervention

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Official Title: Problem Solving Training and Low Vision Rehabilitation

Resource links provided by NLM:


Further study details as provided by National Eye Institute (NEI):

Study Start Date: October 2007
Estimated Study Completion Date: October 2011
Arms Assigned Interventions
Experimental: 1 Behavioral: problem-solving training
Sham Comparator: 2 Behavioral: sham intervention

  Eligibility

Ages Eligible for Study:   19 Years and older
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • +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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00545220

Contacts
Contact: Laura Dreer, PhD 205 325-8681 dreer@uab.edu

Locations
United States, Alabama
University of Alabama at Birmingham Recruiting
Birmingham, Alabama, United States, 35294
Contact: Laura Dreer     205-325-8681     dreer@uab.edu    
Contact: Chris Meek     205-325-8662     gmeek@uab.edu    
Principal Investigator: Laura Dreer, PhD            
Sponsors and Collaborators
University of Alabama at Birmingham
Investigators
Principal Investigator: Laura Dreer, PhD University of Alabama at Birmingham
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00545220     History of Changes
Other Study ID Numbers: X060817006, 5K23EY017327-02
Study First Received: September 21, 2007
Last Updated: October 16, 2007
Health Authority: United States: Institutional Review Board
United States: Federal Government

Additional relevant MeSH terms:
Vision, Low
Vision Disorders
Sensation Disorders
Neurologic Manifestations
Nervous System Diseases
Eye Diseases
Signs and Symptoms

ClinicalTrials.gov processed this record on May 16, 2013