TY - JOUR
T1 - Implementability of a co-designed programme to increase tailored exercise to reduce falls in older people from culturally and linguistically diverse communities
T2 - protocol for a pilot randomised controlled trial
AU - Said, Catherine M.
AU - Ramage, Emily R.
AU - Sharma, Hannah
AU - Batchelor, Frances
AU - Bicknell, Erin
AU - Bongiovanni, Lyn
AU - Brijnath, Bianca
AU - Cahill, Priyanka
AU - Callisaya, Michele
AU - Celestino, Sherisse
AU - Chudecka, Agnieszka
AU - Engel, Lidia
AU - Lim, Wen Kwang
AU - McDonald, Cassie E.
AU - Pinheiro, Marina
AU - Sherrington, Catherine
AU - Vogrin, Sara
AU - Zanker, Jesse
AU - Zheng, Cheng
AU - Klaic, Marlena
AU - MOVE Together: Reduce Falls Collaboration
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2025.
PY - 2025/11/19
Y1 - 2025/11/19
N2 - 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).
AB - 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).
UR - https://www.scopus.com/pages/publications/105022522918
U2 - 10.1136/bmjopen-2025-105995
DO - 10.1136/bmjopen-2025-105995
M3 - Article
C2 - 41263897
AN - SCOPUS:105022522918
SN - 2044-6055
VL - 15
JO - BMJ Open
JF - BMJ Open
IS - 11
M1 - 105995
ER -