Actively Recruiting
Developing Evidence-Based Cognitive Approaches to Improve Adjustment to Vision Loss
Led by The Chicago Lighthouse · Updated on 2025-07-30
45
Participants Needed
1
Research Sites
1 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are developing and testing an 8-week group therapy program that combines cognitive behavioral therapy (CBT) with mindfulness techniques tailored for people adjusting to vision loss. The study aims to create an effective approach to help individuals cope with the emotional and psychological challenges related to vision impairment. The initial phase involves gathering input from focus groups and expert panels to shape the therapy curriculum. During the study, participants will first attend up to two focus group sessions to provide feedback on the therapy content. Following this, a pilot phase will involve 15-20 participants attending weekly group therapy sessions either in person or virtually, based on the developed 8-week curriculum. The therapy combines CBT and mindfulness practices designed specifically for vision loss adjustment. Participants will complete surveys and assessments before and after the therapy, including questions about their vision, demographic information, and experiences related to vision loss. The research team will measure changes in participants' adaptation to vision loss, depression levels, and anxiety before and after the intervention. The total participation period includes the initial feedback sessions and the 8-week therapy program.
CONDITIONS
Brief Title
Developing Evidence-Based Cognitive Approaches to Improve Adjustment to Vision Loss
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults who are at least 18 years old
- Experiencing varying degrees of vision loss such as mild, moderate, or severe
- Willingness to participate in focus groups or pilot testing and provide feedback
You will not qualify if you...
- Severe cognitive impairment affecting participation
- Congenital blindness
- Recent or current participation in another clinical trial or medical intervention that may interfere with study results
- Documented or self-reported health condition that may interfere with study outcomes
- Deemed unfit to participate by the site investigator
- Unwilling or unable to participate or provide consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - 8 weeks
Participants attend eight weekly group therapy sessions combining cognitive behavioral therapy (CBT) and mindfulness practices designed to support adjustment to vision loss.
Weekly group therapy sessions (in-person or virtual) for 8 weeks
Trial Site Locations
Total: 1 location
1
The Chicago Lighthouse
Chicago, Illinois, United States, 60608
Actively Recruiting
Research Team
S
Senior Research Associate
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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