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Optimising rehabilitation outcomes in frail older adults: effects of increasing the amount of physical activity

Does increasing the amount of physical activity in frail older adults during hospital-based rehabilitation improve mobility outcomes when compared to usual care.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613000884707
Acronym
THE MOVE TRIAL
Enrollment
198
Registered
2013-08-08
Start date
2014-01-29
Completion date
2015-04-15
Last updated
2020-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The main aim of this study is to investigate whether increasing the amount of physical activity results in better mobility outcomes in frail, older people. This study will be performed during hospital based rehabilitation and will be compared to mobility outcomes resulting from usual care. A second aim is to investigate whether this physical activity intervention results in improvements in quality of life. Finally we plan to investigate whether increasing the amount of physical activity during rehabilitation is cost effective. Participants will be recruited from two Victorian hospitals which offer inpatient rehabilitation to older adults. Older people receiving inpatient rehabilitation will be randomly assigned to an intervention group or a control group. The intervention group will receive extra physical activity on weekdays and weekends while the control group will receive additional social interaction. Both groups will be assessed at baseline, discharge from hospital and at 6 months. The primary outcome for this study is gait speed, as measured by the 6 metre walk test. Other outcomes relating to mobility, function and quality of life will also be assessed. At the end of the study a health economic analysis will be performed to assess whether the extra physical activity provided was cost effective, all factors considered.

Interventions

In addition to usual care provided by a multidisciplinary rehabilitation team, the intervention group will receive a protocol-specified intervention focused on increasing the amount of time spent standing and walking. This will be delivered as extra sessions on weekdays (1-2 sessions per day, approximate total 30 mins) and weekend days (1-2 sessions, approximate total 45 mins) for the duration of their rehabilitation stay. The intervention will be provided by a trial physiotherapist and or allie

In addition to usual care provided by a multidisciplinary rehabilitation team, the intervention group will receive a protocol-specified intervention focused on increasing the amount of time spent standing and walking. This will be delivered as extra sessions on weekdays (1-2 sessions per day, approximate total 30 mins) and weekend days (1-2 sessions, approximate total 45 mins) for the duration of their rehabilitation stay. The intervention will be provided by a trial physiotherapist and or allied health assistant and tailored for each participant. Intervention adherence will be monitored using staff recordings of the amount of time participants spend performing various activities during each session. Lightweight wristwatch-sized accelerometers will be used to monitor activity of each participant over a 5 day period during their rehabilitation admission.

Sponsors

La Trobe University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

(i) over 60 years of age (ii) a goal of admission is to ‘improve weight-bearing mobility or improve walking’ as determined by either the admission referral or the treating therapist.

Exclusion criteria

(i) specific medical restrictions that limit mobilisation (e.g. non weight bearing) (ii) already enrolled in a different RCT (iii) primary reason for admission is to await a residential care placement (iv) previously enrolled in the current trial (v) primary reason for admission is for carer training

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 18, 2026