Text-message Support to Improve Oral Antibiotic Adherence After ED Discharge
ImpACT
Feasibility of Using Text-Message Support to Improve Antibiotic Adherence After ED Discharge
1 other identifier
interventional
200
1 country
1
Brief Summary
The investigators are testing the hypothesis that patients who are exposed to daily text-message (TM) assessments with feedback will have better adherence to prescription than those patients not exposed to TM-based queries with feedback.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jun 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
June 1, 2011
CompletedFirst Submitted
Initial submission to the registry
July 1, 2011
CompletedFirst Posted
Study publicly available on registry
July 6, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2011
CompletedMay 21, 2012
May 1, 2012
6 months
July 1, 2011
May 18, 2012
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Successfully picked up prescription within 24 hours of ED discharge
We will compare the proporiton of participants in each group who have picked up their prescription within 24 hours of discharge
24 hours post ED discharge
Secondary Outcomes (1)
Complete adherence to oral antibiotics
3-14 days
Study Arms (2)
Mobile phone text message Intervention
EXPERIMENTALDaily assessments with feedback about (1) filling prescription and (2) number of doses taken
Control
NO INTERVENTIONNo TM queries or feedback
Interventions
Daily assessment followed by feedback
Eligibility Criteria
You may qualify if:
- Ages 18 and older
- Planned discharge form the ED on oral antibiotics
You may not qualify if:
- non-English speaking
- Prisoner
- No personal mobile phone with text message features
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
UPMC Mercy Emergency Department
Pittsburgh, Pennsylvania, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 1, 2011
First Posted
July 6, 2011
Study Start
June 1, 2011
Primary Completion
December 1, 2011
Study Completion
December 1, 2011
Last Updated
May 21, 2012
Record last verified: 2012-05