Table 2 In-hospital trauma registry questionnaire, follow-up questionnaires, content, data collection method, and time points (patient-reported outcomes)
From: Exploring the long-term disability outcomes in Trauma patients: study protocol
Questionnaire | Content | Data Collection Method | Data Collection Time point |
|---|---|---|---|
In-hospital Trauma Registry Questionnaire | Demographics, injury details, inter-hospital case management, tracking of patients as he/she moves from emergency (ED) to operation theatre (OT)/High dependency unit (HDU)/ Intensive Care Units (ICU)/wards, Outcomes | Medical Records, In-person interviews | In-hospital and within one week of discharge |
Follow-up questionnaires at one, three, six-, and twelve-months post discharge | |||
Functional Independence Measure (FIM) | Self-care, sphincter control, transfer, locomotion, communication, and social cognition | Telephone Interview with patient/proxy | Within one week of discharge, one, three, six-, and twelve-months post discharge |
Revised Trauma Quality of Life Instrument (RT-QoL) | Emotional well-being, physical well-being, functional engagement | Telephone Interview with patient/proxy | One, three, six-, and twelve-months post discharge |
Primary Care PTSD Screen for DSM | Post-traumatic stress disorder (PTSD) | Telephone Interview with patient/proxy | One, three, six-, and twelve-months post discharge |