Can Tailored Patient Letters Improve The Quality Of Diabetic Patient Care?
1 other identifier
interventional
467
1 country
1
Brief Summary
The purpose of this study is to determine if tailored letters sent to diabetic patients will improve care of diabetes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable diabetes-mellitus
Started Jan 2009
Shorter than P25 for not_applicable diabetes-mellitus
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
January 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2009
CompletedFirst Submitted
Initial submission to the registry
September 24, 2009
CompletedFirst Posted
Study publicly available on registry
September 25, 2009
CompletedSeptember 25, 2009
September 1, 2009
3 months
September 24, 2009
September 24, 2009
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Diabetes summary quality measure
4 months
Study Arms (2)
Tailored letter
EXPERIMENTALPatients in the tailored letter group received by mail a tailored letter detailing their diabetes measures, together with enclosed orders for lab tests when due, and reminder of or scheduling for an office appointment.
Usual Care
ACTIVE COMPARATORPatients in the usual care group were part of a practice wide quality improvement process.
Interventions
Eligibility Criteria
You may qualify if:
- All active patients age 18 to 75 years with a diagnosis of diabetes mellitus were eligible.
- An active patient was defined as one having an ICD-9 code on the active problem list identifying the patient as diabetic, and a progress note in the EMR associated with an office visit within the prior 12 months.
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Scranton-Temple Health Center
Scranton, Pennsylvania, 18510, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
John R Guzek, MD
Scranton-Temple Residency Program
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 24, 2009
First Posted
September 25, 2009
Study Start
January 1, 2009
Primary Completion
April 1, 2009
Study Completion
July 1, 2009
Last Updated
September 25, 2009
Record last verified: 2009-09