Improving Show Rates in Dental Care Settings Serving Underserved Populations (NCT06581250) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Improving Show Rates in Dental Care Settings Serving Underserved Populations
United States48 participantsStarted 2025-04-04
Plain-language summary
The goal of this study is to compare different no-show interventions in dental clinics serving underserved populations. The main question it seeks to answer is
* How do different no-show intervention methods compare in reducing no-shows?
Participants will be asked to
* Implement different interventions
* Report a limited set of data to researchers
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Sites must be:
* Serve at least a 51 percent self-pay and Medicaid patients
* Be willing to provide limited data sets of clinic data to the research team
* Be willing to undertake and support and organizational improvement project to improve show rates
Staff must be:
* A paid staff member at a participating clinic
* Be able and willing to provide written or verbal consent
Exclusion Criteria:
* No exclusion criteria for clinics or staff
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in proportion of scheduled appointments for which the patient attends, pre-to-post intervention
Timeframe: 6 months pre-intervention to 12 months post-intervention