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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03046485
Other study ID # 07-02-013
Secondary ID 07-02-013
Status Withdrawn
Phase N/A
First received October 29, 2010
Last updated February 6, 2017
Start date May 2007
Est. completion date December 2016

Study information

Verified date February 2017
Source Massachusetts Eye and Ear Infirmary
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

120 Patients with visual acuity <6/12 will be randomized to receive either usual care or participate in a 6-week, 2 hour 'Living with Vision Loss' program led by trained leaders. We hypothesize that a structured self-management low-vision rehabilitation program provides a greater improvement in participation in daily activities, and improves quality of life in vision-impaired people compared to the provision of the usual low vision rehabilitation services. We also plan to document barriers that prevent patients with low vision (visual acuity <6/12) from participating in self-management course.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 55 Years to 95 Years
Eligibility Inclusion Criteria:

- Clients who have attended the MEEI Vision Rehabilitation for the first time within 12 months

- Visual acuity of <6/12 in the better eye with habitual correction

- Age 55+ years

- Living independently (not in a nursing home)

- English speaking

- No cognitive impairment

- Adequate hearing to respond to normal conversation

Exclusion Criteria:

- vestibular disease

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Self management program 'Living with Vision Loss'
group met for 6 weeks, 2 hours per week, to discuss strategies for living with low vision

Locations

Country Name City State
United States Vision Rehabilitation Center Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts Eye and Ear Infirmary

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Impact of Vision Impairment Questionnaire (IVI) 1 year
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