Orthopaedic Patient Recognition of Attending Improves Satisfaction Evaluations (Orthopaedic PRAISE Study) (ORTHOPRAISE)
Recruitment status was Not yet recruiting
| Tracking Information | |||||
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| First Received Date ICMJE | December 16, 2010 | ||||
| Last Updated Date | December 20, 2010 | ||||
| Start Date ICMJE | January 2011 | ||||
| Estimated Primary Completion Date | January 2012 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Patient satisfaction [ Time Frame: within 2 weeks of discharge and before first clinic appointment ] [ Designated as safety issue: No ] Within 2 weeks of discharge from the hospital, but before the patient's first clinic visit, each group will be called by the Professional Resource Group as part of regular quality improvement by the Vanderbilt Medical Center Department of Strategic Development. The patients will be asked a series of questions aimed at determining overall patient satisfaction based on interactions with the attending orthopaedic trauma surgeon. |
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| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT01263639 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Orthopaedic Patient Recognition of Attending Improves Satisfaction Evaluations (Orthopaedic PRAISE Study) | ||||
| Official Title ICMJE | Orthopaedic Patient Recognition of Attending Improves Satisfaction Evaluations (Orthopaedic PRAISE Study) | ||||
| Brief Summary | There is a paucity of data in the orthopaedic literature assessing patient satisfaction especially with regards to orthopaedic trauma. Furthermore, the investigators are not aware of any studies looking at utilization of methods to improve the patient's understanding of the primary orthopaedic surgeon that is directing his or her orthopaedic trauma care in order to improve patient satisfaction with overall orthopaedic trauma care. 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. The investigators hypothesize that the biosketch card with the attending orthopaedic trauma surgeon's information and picture will improve the overall patient experience and patient satisfaction by helping to serve as a reminder of the treating surgeon. The reference card can be revisited during the initial hospitalization and even after discharge. The investigators propose that an increased recognition of the treating orthopaedic surgeon will increase patient satisfaction with their inpatient stay. |
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| Detailed Description | The "intervention" group will receive an attending photo/biosketch card within 24 hours of admission while the control group will not. The card will be delivered by a research assistant to the intervention group within 24 hours of admission. The research assistant will not notify the patient that the biosketch card is the intervention in order to maintain the integrity of the study. Furthermore, initiation of the consent process at this point would potentially introduce bias into the study if patients are made aware that we are evaluating their satisfaction based on whether they receive a card. Patients could potentially provide inaccurate and biased answers if required to complete a consent form. As a result, we have applied for a waiver of consent. The investigators will record patient age, gender, and type of injury on admission and will record length of hospital stay. Each patient will randomized to the control group or the "intervention" group and will receive a biosketch card accordingly. Within 2 weeks of discharge from the hospital, but before the patient's first clinic visit, each patient will be called by the Vanderbilt University Medical Center (VUMC) for a patient satisfaction telephone survey. The telephone surveyor will be blinded to the study. After the survey, the patient will be de-identified and the data will be forwarded to our statistician to analyze the data. The primary investigator (PI) and authors will be blinded to the quality improvement survey data until statistical analysis is completed. |
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Not Provided | ||||
| Study Design ICMJE | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator, Outcomes Assessor) |
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| Condition ICMJE | Patient Satisfaction | ||||
| Intervention ICMJE | Other: 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. |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Not yet recruiting | ||||
| Estimated Enrollment ICMJE | 200 | ||||
| Estimated Completion Date | February 2012 | ||||
| Estimated Primary Completion Date | January 2012 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE |
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| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT01263639 | ||||
| Other Study ID Numbers ICMJE | ORTHOPRAISE | ||||
| Has Data Monitoring Committee | Yes | ||||
| Responsible Party | Brent J. Morris, MD, Vanderbilt University Department of Orthopaedic Surgery | ||||
| Study Sponsor ICMJE | Vanderbilt University | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | Vanderbilt University | ||||
| Verification Date | December 2010 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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