Stroke Clinical Trial
Official title:
A Randomized Controlled Trial to Improve the Uptake of and Adherence to Outpatient Rehabilitation Services Among Stroke Patients
Background: Stroke is the leading cause of long-term disability in Singapore, and studies
have found that intensive specialized stroke rehabilitation can improve post-stroke
functional outcomes for a substantial proportion of stroke patients. However, despite the
benefits associated with adherence to prescribed rehabilitation, the uptake rate of
outpatient rehabilitation services (ORS) in Singapore is only 33%.
According to local longitudinal studies, the financial burden of out-of-pocket service costs
and the inconvenient transportation from home to rehabilitation centres are important
barriers to access to ORS.
Objective: To examine the effect and cost-effectiveness of providing incentives for ORS to
improve the uptake of ORS compared to usual care (control) with no incentives
Hypothesis: An evidence-based program to test the effectiveness of providing incentives to
alleviate the financial burden as well as inconvenience of transportation for ORS will
improve the uptake of and adherence to ORS among stroke patients.
Methodology: This study is an individual-based randomized controlled trial (RCT) of 300
stroke patients recruited from Singapore General Hospital (SGH) and Changi General Hospital
(CGH). They will be randomized to one of three study arms (education only, free
transportation, and free services and transportation) and interviewed at the time of
recruitment and four months after the enrolment in the study. Participants' health
conditions, socioeconomic situation, health & medical services utilization, stroke-related
disability measures, quality of life, and reasons for uptake/rejection/withdraw from the
services will be collected during both baseline and the 4th month assessments.
Significance: As the first study in Singapore to test innovative ways to increase the stroke
ORS uptake rates, it will provide evidence for future policy changes in financing outpatient
rehabilitation and other long-term care services in Singapore. It will also provide important
empirical parameter estimates for Systems Dynamics modelling of the demand and supply of ORS
in Singapore.
Background Stroke is the leading cause of long-term disability in Singapore. Stroke accounts
for 9.1% of years of life lost (YLL) and 6.1% of disability-adjusted life years (DALYs). With
a rapidly aging population, the burden of stroke is anticipated to grow correspondingly in
the years to come. Stroke survivors with moderate or severe functional disabilities require
long-term medical and social care, imposing financial and psychological burdens on the
patients and their family members. Research indicates that intensive specialized stroke
rehabilitation can improve post-stroke functional outcomes for a substantial portion of
stroke patients. Extant studies also indicate that rehabilitation is cost-effective in both
inpatient and outpatient settings, and can potentially lead to reductions in both sub-acute
and long-term post-stroke healthcare costs. In addition, a longitudinal study on post-stroke
patients in Singapore found that receiving outpatient rehabilitation service at day
rehabilitation centers resulted in earlier functional recovery. However, despite the benefits
associated with adherence to prescribed rehabilitation sessions, the uptake rate of and
adherence to outpatient rehabilitation service in Singapore is low. Only 33% of stroke
survivors who were recommended for post-discharge community-based rehabilitation actually
took up the service. The low uptake rate also implies substantial potential avoidable
disability among stroke patients in Singapore.
Significance According to a longitudinal survey on patients who were discharged from
community hospital and recommended for post-discharge outpatient rehabilitation in Singapore,
financial burden of rehabilitation services and the inconveniences of transportation are
associated with the low attendance rates to outpatient rehabilitation.
Behavioral economic theory and empirical studies also suggest that the low rate of uptake and
adherence, at least in part, is attributable to stroke patients' perceptions or uncertainty
about the health benefits of rehabilitation. Stroke patients may make a decision to utilize
ORS or not, based on incomplete information about the service attributes (e.g. service
quality, social connectedness, and perceived benefits). Over time, patients and caregivers
may update their perceived service attributes through information and education on stroke
management or actual experiences. Hence, providing incentives to take up ORS and educational
materials on post-stroke management will elevate the current uptake rate of ORS and long-term
adherence.
The proposed study will be the first attempt in Singapore to test innovative ways of
encouraging uptake of stroke ORS. It will systematically test promising economic strategies
that might be effective and cost-effective in increasing the uptake of and adherence to the
prescribed ORS. Given the high bed occupancy rate in public acute hospitals in Singapore,
outpatient center-based rehabilitation service could be a more viable option than inpatient
rehabilitation and more cost-effective in Singapore. It will provide evidence for future
policy change in financing outpatient rehabilitation service and other long-term care
services in Singapore and other countries experiencing similar problems.
Specific Aims & Hypothesis Stroke is the leading cause of long-term disability in Singapore,
and the burden of stroke is posing challenges to the healthcare system and society. Previous
international and regional research studies suggest that a substantial proportion of stroke
patients can benefit from post-stroke rehabilitation services and achieve improved functional
outcomes. However, despite government subsidies and Medisave coverage for outpatient
rehabilitation, the uptake rate of outpatient rehabilitation service (ORS) among stroke
patients is low.
The investigators propose a randomized controlled trial (RCT) to test different interventions
aimed at improving the uptake of and adherence to outpatient rehabilitation services: a
rehabilitation educational program (Group 1, Education), free transportation only (Group 2,
Transportation Incentives) and free transportation and rehabilitation sessions (Group 3,
Transport & Sessions Incentives) for the first 3 months from the date of discharge.
The study aims to:
1. Examine whether incentives for outpatient rehabilitation services (Group 2 and Group 3)
are more effective at improving the uptake of rehabilitation services compared with
education program only (Group 1);
2. Determine whether stroke patients in Group 3 Transport & Sessions Incentives are more
likely to take up ORS than those in the Group 2 Transport Incentives only;
3. Assess the effectiveness of interventions (Group 2 and Group 3) on patient health
outcomes; and
4. Evaluate the cost-effectiveness of the interventions (Group 2 and Group 3) at the 4th
month.
At each recruitment site, the Research Coordinator will assess the patient's eligibility
before approaching them for recruitment. The patient will be given an Abbreviated Mental Test
(AMT) for cognitive assessment. If the patient is cognitively unfit, then his/her
caregiver/proxy will be required to sign the informed consent form on behalf of the patient.
The enrolment period will last for approximately 14-16 months or when the recruitment target
of 300 participants has been achieved.
Baseline Assessment: After signing the informed consent form, the Research Coordinator will
proceed with the baseline assessment which consists of participant's socioeconomic
characteristics, health status, health and medical services utilization, financial status,
stroke-related disability measures, quality of life, and self-efficacy.
The Research Coordinator will educate all participants on their conditions and how to recover
after stroke. A pamphlet with information on post-stroke rehabilitation will also be
distributed to all participants.
Patient-level Intervention: The intervention phase is for a period of three months
post-discharge. The Study Team at Duke-NUS will be coordinating all the incentivised services
for the participants
Measures and Analysis The primary study outcome is uptake of outpatient rehabilitation
services. Uptake is defined as a patient attending at least one rehabilitation session after
discharge. A key secondary outcome will be adherence, defined as the proportion of times the
participant attended prescribed outpatient rehabilitation sessions during the study period.
Additional secondary outcomes of the study include measures of participants' stroke-related
functional status (Modified Rankin Scale, mRS, and modified Barthel Index for Activities of
Daily Living (ADL) limitation), quality of life (EQ-5D), resilience (CD-RISC 10), and
participants' inpatient and other medical services utilization. The investigators will also
obtain participants' baseline socio-demographic data and health status from electronic
medical records and self-reported questionnaire as control variables. In addition, the
program costs of all incentives provided to those in the interventions arms will be tracked
systematically.
The investigators will conduct bivariate analyses and employ generalized linear model to
examine the differences among three study arms in the outcomes of interest, as identified
above. For all the health outcome variables such as, functional status, and will employ a
difference-in-differences (DID) design to assess the impact of incentives. This method
controls for secular trends in outcomes by comparing the longitudinal change in the controls
from the concurrent change in cases between the baseline and follow-up period. Specifically,
the covariates for the interaction term in the regression model (i.e. the
difference-in-differences estimates) represent the difference in the changes over time. In
addition, the incremental cost-effectiveness ratios (ICER) for interventions will be
calculated by dividing the difference in costs of control arm and that of intervention arms
by the incremental effectiveness of both intervention arms compared with control arm.
Power calculation Assuming the uptake rate for control arm is 33% and the detectable
difference for the intervention arm is 10% (that is, the intervention arm that is most
different from control has an uptake rate of 43%), the desired sample size is a total of 300
subjects (100 per arm) to achieve 80% power and to accommodate 10% attrition.
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