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Behavioral Nudges for Cataracts
N/A
Waitlist Available
Led By Catherine A Sarkisian, MD, MSPH
Research Sponsored by University of California, Los Angeles
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 12 months
Awards & highlights
Study Summary
This trial will test whether alerts integrated into the electronic health record can reduce the rate of unnecessary pre-operative testing for cataract surgery.
Who is the study for?
This trial is for patients at UCLA undergoing cataract surgery who also receive their pre-operative evaluation from UCLA Health. It excludes those whose pre-op evaluations are done by non-UCLA physicians.Check my eligibility
What is being tested?
The study tests three 'nudge' alerts integrated into the UCLA Health electronic records, designed to discourage unnecessary pre-op testing for cataract surgery without limiting doctor's choices.See study design
What are the potential side effects?
Since this trial involves behavioral nudges rather than medical treatments, there are no direct physical side effects. However, it may impact decision-making processes in clinical settings.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Secondary outcome measures
Physician Experience Survey Results
Pre-Operative Testing Change
Pre-Operative Testing Change for Specific Categories of Tests
+3 moreTrial Design
4Treatment groups
Experimental Treatment
Group I: ControlExperimental Treatment1 Intervention
Pre-op clinic physicians will not receive interventions and perform duties as usual.
Group II: Alert 3Experimental Treatment1 Intervention
Pre-op clinic physicians will be confronted with nudge #1 if they attempt to place an order for a pre-op test during the pre-op encounter.
Group III: Alert 2Experimental Treatment1 Intervention
Pre-op clinic physicians will be confronted with nudge #1 if they attempt to place an order for a pre-op test during the pre-op encounter.
Group IV: Alert 1Experimental Treatment1 Intervention
Pre-op clinic physicians will be confronted with nudge #1 if they attempt to place an order for a pre-op test during the pre-op encounter.
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Who is running the clinical trial?
RANDOTHER
137 Previous Clinical Trials
509,251 Total Patients Enrolled
University of California, Los AngelesLead Sponsor
1,529 Previous Clinical Trials
10,276,851 Total Patients Enrolled
National Institute on Aging (NIA)NIH
1,671 Previous Clinical Trials
28,016,063 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am having cataract surgery at UCLA and got my pre-op evaluation there.
Research Study Groups:
This trial has the following groups:- Group 1: Alert 2
- Group 2: Alert 3
- Group 3: Control
- Group 4: Alert 1
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are any new participants being added to this research at present?
"According to the data housed on clinicaltrials.gov, this medical study is no longer enrolling. The trial was first released on June 24th 2021 and has not been updated since June 22nd 2022. Nevertheless, there are 124 other trials actively looking for participants at the current time."
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