Implementability of a co-designed programme to increase tailored exercise to reduce falls in older people from culturally and linguistically diverse communities: protocol for a pilot randomised controlled trial

Catherine M. Said, Emily R. Ramage, Hannah Sharma, Frances Batchelor, Erin Bicknell, Lyn Bongiovanni, Bianca Brijnath, Priyanka Cahill, Michele Callisaya, Sherisse Celestino, Agnieszka Chudecka, Lidia Engel, Wen Kwang Lim, Cassie E. McDonald, Marina Pinheiro, Catherine Sherrington, Sara Vogrin, Jesse Zanker, Cheng Zheng, Marlena KlaicMOVE Together: Reduce Falls Collaboration

Research output: Contribution to journalArticleOtherpeer-review

Abstract

Introduction Falls are a critical problem for older people, including those from ethnically diverse communities, who are under-represented in research. The aim of this pilot trial is to evaluate (1) the implementability of a co-designed intervention developed to support the sustained uptake of tailored exercise to reduce falls (MOVE Together: Reduce Falls) and (2) the feasibility of conducting a randomised controlled trial (RCT) in older people from Italian, Arabic, Cantonese or Mandarin-speaking communities. Methods and analysis Investigator and assessor-blinded pilot two-arm parallel RCT. 60 older people at risk of falls from Italian, Arabic, Cantonese or Mandarin speaking communities will be recruited, with the option to enrol on their own or with another participant (dyad). Participants or dyads will be randomly assigned to the experimental or control arm. The experimental arm will receive MOVE Together: Reduce Falls, which provides up to 12 sessions with a physiotherapist over 12 months and supports participants to engage in individualised exercises. Both arms will receive educational resources in the participant’s preferred language. The primary outcome is implementability of the co-designed intervention, MOVE Together: Reduce Falls; operationalised as fidelity (>70% of intended sessions delivered), feasibility (> 95% of sessions delivered with no serious adverse events related or likely related to the intervention) and acceptability (>50% acceptability score). The secondary outcome is feasibility of the RCT protocol, which will be evaluated quantitatively (eg, recruitment and retention rates, completion of clinical outcome data including prospective collection of falls data for 12 months via falls calendars) and qualitatively (eg, barriers and enablers to data collection).

Original languageEnglish
Article number105995
Number of pages10
JournalBMJ Open
Volume15
Issue number11
DOIs
Publication statusPublished - 19 Nov 2025

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