Patient Alert Card

A patient alert card used during a research study is a tool designed to enhance the safety and well-being of participants involved in clinical trials or other types of research studies. It serves several important functions:
  1. Communication Tool: The card provides essential information to healthcare providers about the patient's participation in the research study. This is particularly important if the patient needs emergency medical care or receives treatment from healthcare professionals who are not part of the study team.
  2. Safety Information: The card typically includes details about the study, such as the study title, protocol number, and the study sponsor. It may also contain specific safety information, such as potential side effects or adverse reactions that the patient might experience due to the study intervention.
  3. Contact Information: It lists contact information for the study team, including the principal investigator and other relevant personnel. This allows healthcare providers to quickly reach out for additional information or guidance regarding the patient’s care.
  4. Patient Instructions: The card often includes instructions for the patient, such as what to do in case of an emergency, any precautions they should take, and reminders to show the card to any healthcare provider they visit.
  5. Medical History Integration: By carrying this card, patients ensure that their involvement in the study is considered when other medical treatments are being planned, helping to avoid potential drug interactions or contraindications.
Typical Content of a Patient Alert Card
  • Study Title and Protocol Number: Identifies the specific research study.
  • Patient Identification Number: A unique number assigned to each participant.
  • Study Medication or Intervention: Information about the drug or treatment being studied.
  • Emergency Contact Information: Phone numbers for the study coordinator, principal investigator, and possibly a 24-hour hotline.
  • Key Safety Information: Alerts about specific risks, side effects, or contraindications.
  • Instructions for Healthcare Providers: Guidance on what actions to take and whom to contact in case of emergencies related to the study.

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