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N/A Completed N=749 Health Services Research

Patient Centered Methods to Collect Sexual Orientation and Gender Identity Status in the ED

Homosexuality · Gender Identity
Source: ClinicalTrials.gov NCT02701049 ↗
Enrolled (actual)
749
Serious AEs
0.0%
Results posted
Nov 2018
Primary outcomePrimary: Communication Climate Assessment Toolkit Questionnaire (Patient) — 92.78; 91.32; 94.14 Score

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).

Outcome Measures

OutcomeResultp-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

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
View full record on ClinicalTrials.gov →

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. Informational only — not medical advice.

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