Improving Patient Satisfaction Improving Patient Satisfaction
NCT ID: NCT01263639
Last Updated: 2014-07-28
Study Results
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View full resultsBasic Information
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COMPLETED
NA
228 participants
INTERVENTIONAL
2011-01-31
2012-01-31
Brief Summary
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Design: Prospective quality improvement initiative using a randomized intervention.
Setting: Level 1 academic trauma center.
Patients/Participants: Two hundred twelve patients were eligible; 100 patients were randomized to the intervention group, and 112 patients were randomized to the control group. Overall, 76 patients could be reached for follow-up satisfaction survey, including 34 patients in the intervention group and 42 patients in the control group.
Intervention: Patients randomized to the intervention group received an attending biosketch card, which included a picture of the attending orthopaedic surgeon with a brief synopsis of his educational background, specialty, surgical interests, and research interests.
Main Outcome Measures: Our primary outcome measure was a patient satisfaction survey assessing patients' rating of the overall quality of inpatient care delivered by the attending surgeon.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TRIPLE
Study Groups
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Intervention Group, biosketch card
The investigators aim to improve the patient-physician relationship and improve patient satisfaction by providing a biosketch card of the attending orthopaedic trauma surgeon to the patient. The biosketch card will include a picture of the attending orthopaedic surgeon with a brief synopsis of his or her: education background, specialty, surgical interests, research interests, and other interests including hobbies.
Orthopaedic Attending Biosketch Card
The "intervention" group will receive an attending photo/biosketch card within 24 hours of admission while the control group will not. The biosketch card will include a picture of the attending orthopaedic surgeon with a brief synopsis of his or her: education background, specialty, surgical interests, research interests, and other interests including hobbies.
Control group, standard care
The "intervention" group will receive an attending photo/biosketch card within 24 hours of admission while the control group will not. The control group will receive the usual/standard care as provided to all orthopaedic trauma admission patients without receiving a biosketch card.
Standard of care - No biosketch card
Standard of care
Interventions
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Orthopaedic Attending Biosketch Card
The "intervention" group will receive an attending photo/biosketch card within 24 hours of admission while the control group will not. The biosketch card will include a picture of the attending orthopaedic surgeon with a brief synopsis of his or her: education background, specialty, surgical interests, research interests, and other interests including hobbies.
Standard of care - No biosketch card
Standard of care
Eligibility Criteria
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Inclusion Criteria
* English speaking
* Admitted to the orthopaedic trauma surgery service
* Isolated orthopaedic injury requiring orthopaedic surgery on the same admission
Exclusion Criteria
* traumatic brain injury
* Admission greater than 7 days
* patients with prior orthopaedic trauma injuries treated at Vanderbilt University Medical Center (VUMC)
* patients with prior patient patient-physician relationship with orthopaedic trauma attending
* visually impaired patients
* intubated/sedated patients
* intoxicated patients
18 Years
ALL
No
Sponsors
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Vanderbilt University
OTHER
Responsible Party
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Brent Joseph Morris
Orthopaedic Resident
Principal Investigators
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Brent J Morris, MD
Role: PRINCIPAL_INVESTIGATOR
Vanderbilt University
Locations
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Vanderiblt University Medical Center
Nashville, Tennessee, United States
Countries
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References
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Morris BJ, Richards JE, Archer KR, Lasater M, Rabalais D, Sethi MK, Jahangir AA. Improving patient satisfaction in the orthopaedic trauma population. J Orthop Trauma. 2014 Apr;28(4):e80-4. doi: 10.1097/01.bot.0000435604.75873.ba.
Other Identifiers
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Clinical Trial
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
Patient Satisfaction
Identifier Type: -
Identifier Source: org_study_id
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