Background: Patient-reported outcomes are integral to understanding the burden of stroke. The Australian Stroke Clinical Registry (AuSCR) collects patient outcomes 90-180 days after stroke/TIA, however current data collection methods via mail and telephone are resource intensive.
Aims: To determine whether the added procedure of an SMS sent 4-weeks after the first mailout with a link to complete the survey electronically is feasible and efficient for collecting health outcome data.
Methods: Eligible patients from 27 hospitals registered in the AuSCR were randomised 1:1 to the standard follow-up process (two paper-based surveys by mail 6 weeks apart then contact by phone if no response) or to the new SMS protocol. Descriptive statistics were used to compare within and between group differences (chi-squared or Wilcoxon rank-sum tests).
Results: Overall 1,008 registrants were randomised and had similar profiles (58% male, median age 72 years). Eight were excluded post-randomisation and removed at the hospitals’ request because the final diagnosis was not stroke/TIA. In the SMS group, 18% completed the survey via the SMS link. Overall follow-up completion was 11% greater in the SMS group compared to the standard group. Those who responded in the SMS group had a median response time that was 14 days shorter than the control group (p<0.05). The median age of SMS group participants that completed the survey via the SMS link was younger that those who completed by other methods (69 vs 74 years, p=0.03). Missing data were similar between groups.
Conclusion: Collecting patient-reported outcomes via an electronic survey sent by SMS was feasible; benefits included increased response rates and shorter time to completion. The younger median age of responders via electronic methods may indicate a preference over current methods. The use of SMS has now been adopted by the AuSCR as part of the follow-up protocol.