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Low-vision rehabilitation program for Low Vision

N/A
Waitlist Available
Led By Monali Malvankar
Research Sponsored by Lawson Health Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline up to 24 weeks
Awards & highlights

Summary

To evaluate health related quality of life (HRQoL) of low-vision patients and their care givers undergoing low-vision rehabilitation program (LVRP).

Eligible Conditions
  • Low Vision
  • Low Vision Aids

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline up to 24 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and change from baseline up to 24 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in Health related Quality of Life (HRQoL)
Secondary study objectives
Change in Anxiety Score
Change in Depression Score
Change in Low vision Score

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Low-vision rehabilitation programActive Control1 Intervention
Participants and their care givers in Low-vision rehabilitation program will undergo a standardized interview to measure HRQoL using the time trade-off method (TTO), depression using the Patient Health Questionnaire (PHQ-9), anxiety using Generalized Anxiety Disorder (GAD-7) and Veterans Affairs Low Vision Visual Functioning Questionnaire (VA LV VFQ-48) at the first study visit and after Low-vision rehabilitation program.
Group II: No InterventionPlacebo Group1 Intervention
Participants and their care givers will undergo a standardized interview to measure HRQoL using the time trade-off method (TTO), depression using the Patient Health Questionnaire (PHQ-9), anxiety using Generalized Anxiety Disorder (GAD-7) and Veterans Affairs Low Vision Visual Functioning Questionnaire (VA LV VFQ-48) at the first study visit and will continue to receive treatment as usual.

Find a Location

Who is running the clinical trial?

Lawson Health Research InstituteLead Sponsor
672 Previous Clinical Trials
414,361 Total Patients Enrolled
Monali MalvankarPrincipal InvestigatorWestern University, Canada
3 Previous Clinical Trials
635 Total Patients Enrolled
~21 spots leftby Sep 2025