Managing Side Effects in Clinical Practice | NCT03475550 | Trialant

Managing Side Effects in Clinical Practice | NCT03475550 | Trialant

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Standard of care 1	Active Comparator	Patients will receive one of 2 different descriptions of the medication's risks and benefits. Both descriptions meet ethical standards of transparency and respect for person and are commonly used but have never been compared. "Standard of Care 1" includes more details than "Standard of Care 2".	Other: Standard of Care
Standard of care 2	Active Comparator	Patients will receive one of 2 different descriptions of the medication's risks and benefits. Both descriptions meet ethical standards of transparency and respect for person and are commonly used but have never been compared. "Standard of Care 2" includes fewer details than "Standard of Care 1".	Other: Standard of Care

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Standard of Care	Other	The intervention involves clinician-provided information to patients receiving a new medication as part of their standard medical care. Intervention 1 includes more detailed information compared to Intervention 2.

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Patient-reported benefit from the drug	Visual Analog Scale of reported benefit from the drug (0-10)	3 weeks after the physician visit
Number of side effects reported from the drug	Checklist of reported side effects from the drug	3 weeks after the physician visit

Contacts/Locations Module

Intervention Browse Module