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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00013403
Other study ID # C1998R
Secondary ID
Status Completed
Phase Phase 2
First received March 14, 2001
Last updated June 25, 2015
Start date April 1999
Est. completion date March 2002

Study information

Verified date June 2015
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The project has four primary objectives: 1) Determine if blind rehabilitation improves the quality of life of legally blind veterans; 2) Determine the relationship between quality of life and visual function; 3) Determine if factors, such as cognitive status, level of depression, age and the presence of additional medical conditions besides vision loss, intervention of blind rehabilitation extends beyond the visually impaired individual and improve the quality of life of their primary caregiver (e.g. spouse, partner, family member or friend.)


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date March 2002
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Visually impaired

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Blindness


Locations

Country Name City State
United States VAMC, Birmingham Birmingham Alabama

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

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