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Help Optimise and Mobilise Elders (H.O.M.E)

Help Optimise and Mobilise Elders (H.O.M.E)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05484063
Acronym
HOME
Enrollment
90
Registered
2022-08-02
Start date
2022-07-25
Completion date
2023-09-30
Last updated
2022-08-02

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

Conditions

Functional Disturbance, Mobility Limitation

Keywords

Elderly, Geriatric, Mobility, Inpatient, Functional Decline, Mobility Intervention, Gait speed, Maximum distance walked, Cost impact, length of stay, Multidisciplinary, Implementation study, 4Ms (Mobility, Mentation, Medication, What Matters), Nursing screen, Group therapy

Brief summary

During hospitalisations, older inpatients commonly face issues such as immobility, loss of independence, and functional decline. This leads them down the cascade of dependency with consequent increased risk of adverse outcomes, institutionalisation as well as higher post-acute care costs. The investigators hypothesize that by implementing a mobility intervention in the inpatient setting, patients would be able to maintain their function upon discharge and avoid the cascade of dependency. As such, the investigators aim to do this by implementing and evaluating a mobility intervention, while optimising reversible factors affecting mobility among inpatients admitted to a geriatric unit in Singapore. The investigators will also examine the cost impact of a mobility focused model of care and also adopt the effectiveness-implementation hybrid Type 2 design where both effectiveness and implementation spheres are tested simultaneously.

Detailed description

Aim 1: To examine the effectiveness of multicomponent, mobility-focused model of care in reducing iatrogenic complications and improving patient outcomes. Adopting the Institute for Healthcare Improvement's (IHI) 4Ms framework (Mobility, Mentation, Medication, and What Matters), the investigators will examine the effectiveness of timely and individually catered mobility interventions which not only increase mobilization but also optimize factors inhibiting mobility for elderly inpatients. It is hypothesized that the mobility outcomes, such as maximum distance walked and mobilization frequency will be significantly improved for patients who receive the intervention compared to those who receive standard care. Aim 2: To examine the cost impact of a mobility-focused model of care. The investigators will examine whether the cost of these multicomponent, mobility-focused interventions can be offset from cost savings from early mobilisation benefits, by comparing healthcare utilization costs between-groups. Further to that, a cost effectiveness analysis will be performed should functional effectiveness be observed. For the primary cost impact objective, it is hypothesized that the cost savings arising from reduction in bed days of hospitalization and other medical costs incurred during study period will outweigh the cost of implementing this model of care. In addition, it is also hypothesized that the proposed intervention will be cost-effective through achieving better functional outcomes for patients, with lower costs required. Aim 3: To evaluate the implementation outcomes of multicomponent, mobility-focused model of care in the process of this intervention. It is hypothesized that this intervention will have good acceptability, feasibility, penetration, implementation costs and sustainability.

Interventions

OTHERMulticomponent, mobility-focused intervention

The intervention group will receive early therapist review (within one working day of admission to HOME unit), to be mobilised at least three times a day. They will also receive additional group exercise therapy sessions, as well as nurse screening for geriatric syndromes. Besides that, they will be screened for 4Ms (Mobility, Mentation, Medication, What Matters) by doctor on admission.

Sponsors

Geriatric Education and Research Institute
CollaboratorOTHER_GOV
National Healthcare Group, Singapore
CollaboratorOTHER_GOV
JurongHealth
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

It is a quasi-experimental design study.

Eligibility

Sex/Gender
ALL
Age
21 Years to 110 Years
Healthy volunteers
Yes

Inclusion criteria

* Newly admitted patients to the geriatric service * Aged 75 years and above * Mobile with or without the use of a walking aid

Exclusion criteria

* Vancomycin-resistant enterococcus (VRE) status * Requires droplet or airborne precautions * Critically ill * Haemodynamically instability * Requires more than 4-hourly parameters * Systolic blood pressure \<90 mmHg * Heart rate \>100beats/min * Non-ambulant patients * With advanced dementia (Functional Assessment Staging Scale \[FAST\] 7 dementia) * Fulfills direct admission to another subspecialty unit

Design outcomes

Primary

MeasureTime frameDescription
Change in maximum distance walkedUpon admission and at the point of discharge (an average of 10 days after inclusion. Analysis will take into account the variability of length of stay)The total distance covered by the research participant (in meter)
Mobilisation frequencyThrough the duration of admissionNumber of times mobilised. The average mobilisation frequency will be calculated by dividing the sum by the number of admission days.

Secondary

MeasureTime frameDescription
Change in gait speedUpon admission and at discharge (an average of 10 days after inclusion. Analysis will take into account the variability of length of stay)4 meter gait speed test (meter/second)
Change in modified barthel scoreUpon admission, at discharge (an average of 10 days after inclusion. Analysis will take into account the variability of length of stay), and one-month post dischargeThe score ranges from 0 to 100 with 0 as the worst outcome
Inpatient length of stay and discharge locationThe duration of admission and upon discharge (an average of 10 days after inclusion. Analysis will take into account the variability of length of stay)The duration of admission (days) and the location the respective participant is discharged to
Presence of common iatrogenic complications such as delirium, injurious falls, pressure ulcers, and venous thromboembolismsAt discharge (an average of 10 days after inclusion. Analysis will take into account the variability of length of stay)Each of the complication will be measured in nominal scale; 0 denotes the absence of the complication while 1 denotes the presence of the complications. The total number of complications arise will be calculated. The greater the number indicates poorer outcome
Gross amount of patient's bill during index admission, considering subsidy levelAt discharge (an average of 10 days after inclusion. Analysis will take into account the variability of length of stay)The total gross amount of participant's bill during index admission. The subsidy level will be documented
The intervention related costs for group therapyAt discharge (an average of 10 days after inclusion. Analysis will take into account the variability of length of stay)The number of group therapy sessions attended by the participant multiply by the cost for one group therapy session. The subsidy level will be documented.

Other

MeasureTime frameDescription
Healthcare utilisation data and associated costs1-month follow-up post-dischargeNumber of visits (associated with index admission) to emergency department, specialist outpatient clinic, general practitioner and the associated costs within 30 days post-discharged
Ambulatory status1-month follow-up post-dischargeSelf-reported by the participant. Four options: 0 denotes bed-bound, 1 denotes chair-bound, 2 denotes assisted (furniture cruiser, walking frame, rollator frame, quadstick, single point stick); 4 denotes independent
Fall1-month follow-up post-discharge0 denotes no fall; 1 denotes fall(s) occured (within 30days post-discharged)
Utilisation of community resources1-month follow-up post-dischargeSelf-reported by the participant: Five options: 0 denotes home care; 1 denotes day care; 2 denotes meals on wheels; 3 denotes medical escort service; 4 denotes home personal care
Readmission1-month follow-up post-dischargeThe number of readmission due to the index admission within 30 days post discharged
Mortality1-month follow-up post-discharge1 denotes survival while 0 denotes the participant passed away

Countries

Singapore

Contacts

Primary ContactMelanie Tan Dr
melanie_tan@nuhs.edu.sg67165237

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 19, 2026