N/A
N=749
Patient Centered Methods to Collect Sexual Orientation and Gender Identity Status in the ED
Homosexuality · Gender Identity
Bottom Line
View on ClinicalTrials.gov: NCT02701049 ↗Enrolled (actual)
749
Serious AEs
0.0%
Results posted
Nov 2018
Primary outcome: Primary: Communication Climate Assessment Toolkit Questionnaire (Patient) — 92.78; 91.32; 94.14 Score
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Methods to collect SO/GI information in the ED (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Brigham and Women's Hospital
- Primary completion
- Mar 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Communication Climate Assessment Toolkit Questionnaire (Patient) |
92.78; 91.32; 94.14 | — |
| SECONDARY Staff-reported Outcomes Measure Questionnaire |
11; 14; 16; 14; 7; 8 | — |
| SECONDARY Proportion of Patients Reporting SO/GI |
228; 132 | — |
Summary
This trial is the final phase of a three phase PCORI-funded study to develop and test patient-centered approaches to collect sexual orientation and gender identity (SO/GI) information in the ED. From the results of Phase 1 qualitative interviews and national quantitative survey and Phase 2 Delphi rounds with the Stakeholder Advisory Board, we have determined two methods of collection favored by patients and providers to implement in the trial. The first method, nurse verbal collection, is in alignment with Partners recommended clinical practice and is therefore a quality improvement (QI) evaluation. The second method, non-verbal registrar form collection with nurse verbal confirmation, is a research intervention to evaluate and compare a new patient-centered approach to SO/GI collection. To compare the patient-centeredness of the two different approaches, satisfaction surveys will be administered to ED patients and staff members involved in collection.
In summary, the study design (1) evaluates recommended current practice (QI), (2) evaluates a quality improvement project to increase recommended current practice, and (3) evaluates a new method of collecting SO/GI (research intervention).
Eligibility Criteria
Inclusion Criteria
- Adult ED patients who are cognitively and physically capable of informed consent
- Adult ED nurses and registrars who are cognitively and physically capable of informed consent
Exclusion Criteria
- Children
- Any person not cognitively and physically capable of informed consent
Data sourced from ClinicalTrials.gov (NCT02701049). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.