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Withdrawn project - did not progress to enrollment.
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Patients in the orthopedic surgery clinic routinely fill out a patient- reported outcome measurement survey prior to their visit. These scores are stored in Epic, but are not routinely reviewed with patients during their office visit. Study subjects will be randomly assigned into one of two groups: those who have their patient- reported outcome measurements reviewed with them by their physician, and those who will not have their patient-reported outcome measurements reviewed during the visit. Following the visit, patients will complete a patient satisfaction survey.
This patient satisfaction survey is a modified version of the Press-Ganey Outpatient Medical Practice 10-question survey. The patient satisfaction survey scores will then be compared between the two groups to quantify the effect of reviewing of patient-reported outcome measurements with patients on their satisfaction with the office visit
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Standard of care group | No Intervention | Participants who did not have their physicians review their patient-reported outcome measurements with them during the office visit. | |
| Consultation group | Experimental | Participants who had their physicians review their patient-reported outcome measurements reviewed with them during the office visit. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Review | Behavioral | Physicians will review patient-reported outcome measurements with their patients during office visits. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in participants' satisfaction | Participants' satisfaction will be measured by completing a patient satisfaction survey. This patient satisfaction survey is a modified version of the Press-Ganey Outpatient Medical Practice 10-question survey. The patient satisfaction survey scores will then be compared between the two groups to quantify the effect of reviewing of patient-reported outcome measurements with patients on their satisfaction with the office visit. | 1 day (Visit 1) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Andrew Rokito, MD | NYU Langone Health | Principal Investigator |
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All of the individual participant data collected during the trial, after deidentification.
condition of awards and agreements supporting the research.
Investigators whose proposed use of the data has been approved by an independent review committee ("learned intermediary") identified for this purpose. Upon reasonable request. Requests should be directed to andrew.rokito@nyulangone.org. To gain access, data requestors will need to sign a data access agreement.
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| ID | Term |
|---|---|
| D054198 | Precursor Cell Lymphoblastic Leukemia-Lymphoma |
| ID | Term |
|---|---|
| D007945 | Leukemia, Lymphoid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
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| D006402 |
| Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |