The effect of remote treatment on medical provider creative thinking and patient disclosure: protocol for the MED-CREATE trial
Unlocking Enhanced Healthcare: Remote Treatment and its Impact
This groundbreaking study protocol (MED-CREATE trial) explores the dual impact of remote treatment modalities on medical provider creativity and patient disclosure, aiming to optimize telehealth strategies for improved patient care.
Strategic Implications for Healthcare Delivery
The MED-CREATE trial offers critical insights for healthcare executives seeking to leverage telehealth effectively. Understanding the trade-offs between online and in-person consultations can drive strategic resource allocation and enhance patient outcomes.
Key Strategic Benefits
- Informing telehealth policy and infrastructure development.
- Optimizing clinician training programs for virtual care.
- Tailoring communication strategies for sensitive patient disclosures.
- Enhancing diagnostic accuracy in remote settings.
Deep Analysis & Enterprise Applications
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The study aims to recruit 194 medical student-patient dyads (388 participants total) to ensure statistically significant findings on communication modality.
MED-CREATE Trial Design Flow
| Aspect | Online (Hypothesized) | Offline (Hypothesized) |
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| Creative Idea Generation |
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| Patient Disclosure |
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| Clinician Factors |
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| Patient Factors |
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Addressing Diagnostic Challenges in Telehealth
A core objective of the MED-CREATE trial is to examine how communication modality impacts clinicians' ability to generate solutions to complex clinical problems. Previous research suggests that online interactions may inhibit creative thinking, which is crucial for differential diagnosis and identifying rare conditions. By simulating challenging patient cases, the study will provide empirical evidence on whether telehealth platforms hinder or support the diagnostic process, particularly when divergent thinking and problem sensitivity are required.
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MED-CREATE Trial Execution Phases
Phase 1: Setup & Recruitment
Finalize IRB approval, recruit medical students and acting patients, establish secure online and in-person consultation environments, and configure REDCap for data management.
Phase 2: Data Collection
Conduct randomized controlled consultations, collect baseline psychometric data, record interactions, and administer post-consultation questionnaires.
Phase 3: Data Processing & Analysis
Transcribe audio recordings, anonymize data, perform statistical analysis on primary and secondary outcomes using R, and interpret findings.
Phase 4: Dissemination & Reporting
Publish results in peer-reviewed journals, present at scientific conferences, and make de-identified data and analysis code publicly available.
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