Video Assisted Informed Consent for Lortab to Improve Patient Satisfaction and Knowledge
2 other identifiers
interventional
120
1 country
1
Brief Summary
In order to compare two different forms of patient education; patients who receive Lortab medication or prescription during their ED visit are randomized to receive either standard patient education (from healthcare provider) or video assisted education. After education, patient completes a survey, estimated to take 5 minutes to complete.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2011
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2011
CompletedFirst Submitted
Initial submission to the registry
June 7, 2011
CompletedFirst Posted
Study publicly available on registry
June 15, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2012
CompletedMarch 24, 2014
June 1, 2011
10 months
June 7, 2011
March 21, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
patient satisfaction and knowledge
comparison of patient completed survey following education via standard format or 3 minute video
survey is completed immediately after education, estimated time to complete survey is 5 minutes
Study Arms (2)
video
EXPERIMENTALIf randomized to this arm patient watches a 3 minute video
standard education
ACTIVE COMPARATORIf randomized to this arm patient receives standard verbal education from healthcare provider.
Interventions
Receives standard verbal education from healthcare provider
Eligibility Criteria
You may qualify if:
- non-critical emergency room patients being prescribed Lortab
- age 18 year or older
You may not qualify if:
- emergency room patients not receiving Lortab as their first prescribed medication
- age less than 18 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Albany Medical Center
Albany, New York, 12208, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor Dept. of Emergency Medicine
Study Record Dates
First Submitted
June 7, 2011
First Posted
June 15, 2011
Study Start
March 1, 2011
Primary Completion
January 1, 2012
Study Completion
January 1, 2012
Last Updated
March 24, 2014
Record last verified: 2011-06