Poster Presentation Australian and New Zealand Society for Geriatric Medicine Annual Scientific Meeting 2026

Sleepless in a Geriatric Rehabilitation Unit: A Hidden Burden in Older Inpatients (#236)

Olivia B Ogilvy Dunstan 1 2 3 , Adrienne Young 1 2 3 , Ruth Eleanor Hubbard 1 2 3 4 , Claire M Ellender 1 2 5
  1. The University Of Queensland, Brisbane, QLD, Australia
  2. Faculty of Health, Medicine, and Behavioural Sciences, Centre for Health Services Research, Brisbane, Queensland, Australia
  3. Australian Frailty Network, Brisbane, Queensland, Australia
  4. Department of Geriatric Medicine, Princess Alexandra Hospital, Brisbane, Queensland, Australia
  5. Department of Respiratory & Sleep Medicine, Princess Alexandra Hospital , Brisbane, Queensland, Australia

Aims: To estimate the prevalence and correlates of Pittsburgh Sleep Quality Index (PSQI)-defined poor sleep in geriatric rehabilitation inpatients, and to compare 72-hour actigraphy between PSQI groups.

Methods: Prospective observational cohort study in a metropolitan geriatric rehabilitation unit (November 2024 to November 2025), embedded within a larger program assessing the ward environment (light/ sound), and co-designing and implementing a multicomponent non-pharmacological sleep intervention. Participants aged 60-95 years completed the PSQI, Insomnia Severity Index (ISI), Depression-Anxiety-Stress Scales-21 (DASS-21), Short Form-36 (SF-36), and wore a wrist ActiGraph for 72 hours. Poor sleep was defined PSQI >5. Logistic regression produced odds ratios (ORs) with 95% confidence intervals (CIs). Actigraphy comparisons were conducted in the valid recording subset (n=45).

Results: Mean global PSQI was 9.87. Poor sleep occurred in 52/62 participants (83.9%), yet documented prior sleep disorder diagnoses were uncommon (13/62, 21%). Odds of poor sleep increased with ISI (OR 1.32 per point, 95% CI 1.09–1.69; p=0.0018) and DASS-21 Anxiety (OR 1.17 per point, 95% CI 1.01–1.45; p=0.0398), and higher SF-36 scores were associated with lower odds (OR 0.92 per point, 95% CI 0.84–0.99; p=0.023). In the actigraphy subset (n=45), total sleep time was 88.4 minutes lower in poor sleepers than good sleepers (95% CI -169.2 to -7.6; p=0.033); sleep onset latency, wake after sleep onset, and sleep efficiency did not differ significantly.

Conclusions: Self-reported sleep disturbance was highly prevalent yet under-recognised in this geriatric rehabilitation cohort. Findings support routine sleep assessment, proactive medication review, and tailored non-pharmacological strategies, with selective use of actigraphy.