Use of Self-management Group to Improve Quality of Life in Patients With Low Vision

NCT ID: NCT03046485

Last Updated: 2017-02-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2007-05-31

Study Completion Date

2016-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Age Related Macular Degeneration

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Self management program

Self management program 'Living with Vision Loss' 6 week course that met for 2 hours each week led by a trained leader.

Group Type EXPERIMENTAL

Self management program 'Living with Vision Loss'

Intervention Type BEHAVIORAL

group met for 6 weeks, 2 hours per week, to discuss strategies for living with low vision

Wait list control

Wait list control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Self management program 'Living with Vision Loss'

group met for 6 weeks, 2 hours per week, to discuss strategies for living with low vision

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

55 Years

Maximum Eligible Age

95 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Massachusetts Eye and Ear Infirmary

OTHER

Sponsor Role lead

Responsible Party

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Mary Lou Jackson

principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mary Lou Jackson, MD

Role: PRINCIPAL_INVESTIGATOR

MEEI Vision REhabilitation Center Dir.

Locations

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Vision Rehabilitation Center

Boston, Massachusetts, United States

Site Status

Countries

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United States

Other Identifiers

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07-02-013

Identifier Type: OTHER

Identifier Source: secondary_id

07-02-013

Identifier Type: -

Identifier Source: org_study_id

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