Enhancing Engagement by Integrating Goals and Concerns That Matter to Patients (NCT06898593)
🩺 Plain-English Summary (8th-Grade Level)
The goal of this clinical trial is to learn if adding patients' goals and concerns to measurement-based collaborative care can tailor care and provide a more holistic view of treatment, thereby improving engagement in care among adult patients receiving collaborative care. The main questions it aims to answer are: * Does using a clinical decision support system (which includes an enhanced pre-visit questionnaire and patient-level dashboard) improve patient engagement in the collaborative care model? * Does using a clinical decision support system improve patient and clinician satisfaction with care? Researchers will compare the enhanced collaborative care with traditional collaborative care. Patient participants will complete pre-visit questionnaires before their collaborative care appointments. Responses will be viewed by the clinician and/or patient in a visual dashboard inside the electronic health record.
Who can join: Review the eligibility criteria below.
Location: Dartmouth Hitchcock Concord Family Medicine — Concord, New Hampshire
Age range: 18 Years to 100 Years
🧪 Interventions in This Study
- Collaborative care model with clinical decision support system (BEHAVIORAL)
- Collaborative care model (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (6 Sites)
- Dartmouth Hitchcock Concord Family Medicine — Concord, New Hampshire
- Dartmouth Hitchcock Medical Center — Lebanon, New Hampshire
- Dartmouth-Hitchcock Heater Road Internal Medicine — Lebanon, New Hampshire
- Dartmouth Hitchcock Manchester Family Practice — Manchester, New Hampshire
- Dartmouth Hitchcock Nashua Family Practice — Nashua, New Hampshire
- Dartmouth Hitchcock Nashua General Internal Medicine — Nashua, New Hampshire
📞 Contact the Study Coordinator
Phone: (603) 646-5449
Email: irina.perreard@dartmouth.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.