Clinical trial · Interventional
Application of Intelligent Care Systems in Radiation Therapy: Enhancing Patient Safety and Reducing Anxiety Through System Optimization and Real-Time Blood Data Monitoring
Application of Intelligent Care Systems in Radiation Therapy: Enhancing Patient Safety and Reducing Anxiety Through System Optimization, Enhanced Education Strategies, and Real-Time Blood Data Monitoring
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study aims to evaluate the impact of an intelligent care system on radiation therapy patients, focusing on real-time blood data monitoring, optimized patient education, and internal alert systems. The goal is to enhance patient safety, improve treatment adherence, and reduce anxiety by integrating an alert function into the hospital's existing system. Key interventions include: Real-time blood monitoring alerts: Healthcare providers will receive automatic notifications of abnormal blood test results to ensure timely intervention. Optimized patient education materials: Clearer guidance will help patients proactively communicate blood test needs and manage their health during radiation therapy. Internal reminders: Visual signs and alerts in treatment areas will reinforce patient awareness and engagement. The study will compare patients receiving these interventions with those under standard care, assessing treatment compliance, anxiety levels, and clinical outcomes over a 12-month period.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Adherence | — | UNRESOLVED | — |
| Anxiety | — | UNRESOLVED | — |
| Chemoradiotherapy | — | UNRESOLVED | — |
| Radiation Therapy | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Enhanced Patient Education Materials (Behavioral/Educational Intervention) | Behavioral | — | UNRESOLVED |
| Internal Warning Signs and Alerts (Behavioral Intervention) | Behavioral | — | UNRESOLVED |
| Real-Time Blood Data Monitoring System (Device/Software Integration) | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Intelligent Care System Group (Intervention Group)
- description
- Participants in this group will receive an optimized intelligent care system designed to enhance patient safety, improve treatment adherence, and reduce anxiety during radiation therapy. This system includes real-time blood data monitoring alerts, enhanced patient education materials, and internal warning reminders.
- interventionNames
- Device: Real-Time Blood Data Monitoring System (Device/Software Integration)
- Behavioral: Enhanced Patient Education Materials (Behavioral/Educational Intervention)
- Behavioral: Internal Warning Signs and Alerts (Behavioral Intervention)
- type
- NO_INTERVENTION
- label
- Standard Care Group (Control Group)
- description
- Participants in this group will receive standard care without the optimized intelligent care system interventions. They will continue their treatment following existing clinical practices without additional automated monitoring or enhanced education strategies.
Primary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: * Patients undergoing radiation therapy combined with chemotherapy. * Age ≥ 18 years. * Ability to understand and comply with the study protocol. * Willing to participate in the study and provide informed consent. Exclusion Criteria: * Patients with severe cognitive impairment or intellectual disability, affecting their ability to understand or follow study procedures. * Patients unwilling to complete study questionnaires. * Any mental health condition (e.g., major depressive disorder, severe anxiety disorder) that could interfere with participation. * Patients with conditions requiring immediate intervention that would make study participation impractical.
References
Publications (0)
Data not yet available