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Stroke Patients' Outpatient Rehabilitation Therapy (SPORT) (SPORT)

Primary Purpose

Stroke, Incentives, Stroke Rehabilitation

Status
Completed
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
Transportation incentives
Transportation and rehabilitation services incentives
Sponsored by
National University of Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Stroke

Eligibility Criteria

55 Years - 100 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Diagnosed with stroke as defined by the World Health Organization's criteria;
  • Discharged to home;
  • Recommended by physicians to continue outpatient rehabilitation afte discharge;
  • Singapore citizen or Permanent Resident; and
  • Provision of informed consent.

Exclusion Criteria:

  • Stroke patients who are suffering from severe dysphasia without caregiver or proxy;
  • Cognitively impaired patients without caregiver or proxy; and
  • Age < 20 years.

Sites / Locations

  • Changi General Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Group 1

Group 2

Group 3

Arm Description

Education or Control group.

Transportation incentives

Transportation and rehabilitation services incentives

Outcomes

Primary Outcome Measures

Uptake rate of incentivised rehabilitation services
Uptake rate of incentivised services will be measured by number of participants who attend at least one rehabilitation session.

Secondary Outcome Measures

Adherence rate of incentivised rehabilitation services
Adherence rate will be measured by the proportion of recommended sessions participants attended versus number of sessions recommended.
Barriers for outpatient rehabilitation services (ORS) utilization
ORS take-up rate between Group 2 and Group 3 will be computed to assess if transportation or out of pocket costs are barriers for ORS.
Effectiveness of interventions on participants' health outcomes
The investigators will be using Modified Barthel Index to measure health outcomes, comparing the changes from baseline to assessment at 4th month.
Cost effectiveness of incentivised ORS
The investigators will be using the cost data collected from rehabilitation centres and actual costs for the incentivised ORS to assess cost effectiveness. Incremental cost-effectiveness ratio (ICER) will be computed using the extra cost with incentives ($) / Improved uptake rate of rehabilitation with incentives (% attending at least one session).

Full Information

First Posted
May 16, 2017
Last Updated
February 24, 2020
Sponsor
National University of Singapore
Collaborators
Ministry of Health, Singapore, Duke-NUS Graduate Medical School, Changi General Hospital, Singapore General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03165630
Brief Title
Stroke Patients' Outpatient Rehabilitation Therapy (SPORT)
Acronym
SPORT
Official Title
A Randomized Controlled Trial to Improve the Uptake of and Adherence to Outpatient Rehabilitation Services Among Stroke Patients
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
May 26, 2017 (Actual)
Primary Completion Date
November 30, 2019 (Actual)
Study Completion Date
November 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National University of Singapore
Collaborators
Ministry of Health, Singapore, Duke-NUS Graduate Medical School, Changi General Hospital, Singapore General Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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: 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); 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; Assess the effectiveness of interventions (Group 2 and Group 3) on patient health outcomes; and 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Incentives, Stroke Rehabilitation

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The 4th month assessor is unaware of the arm participants are assigned to.
Allocation
Randomized
Enrollment
266 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
No Intervention
Arm Description
Education or Control group.
Arm Title
Group 2
Arm Type
Experimental
Arm Description
Transportation incentives
Arm Title
Group 3
Arm Type
Experimental
Arm Description
Transportation and rehabilitation services incentives
Intervention Type
Behavioral
Intervention Name(s)
Transportation incentives
Intervention Description
Free transportation only for the first 3 months post-discharge.
Intervention Type
Behavioral
Intervention Name(s)
Transportation and rehabilitation services incentives
Intervention Description
Free transportation and rehabilitation services 3 months post-discharge.
Primary Outcome Measure Information:
Title
Uptake rate of incentivised rehabilitation services
Description
Uptake rate of incentivised services will be measured by number of participants who attend at least one rehabilitation session.
Time Frame
3 months post-discharge
Secondary Outcome Measure Information:
Title
Adherence rate of incentivised rehabilitation services
Description
Adherence rate will be measured by the proportion of recommended sessions participants attended versus number of sessions recommended.
Time Frame
3 months post-discharge
Title
Barriers for outpatient rehabilitation services (ORS) utilization
Description
ORS take-up rate between Group 2 and Group 3 will be computed to assess if transportation or out of pocket costs are barriers for ORS.
Time Frame
3 months post discharge
Title
Effectiveness of interventions on participants' health outcomes
Description
The investigators will be using Modified Barthel Index to measure health outcomes, comparing the changes from baseline to assessment at 4th month.
Time Frame
Change from Baseline MBI at 4 months
Title
Cost effectiveness of incentivised ORS
Description
The investigators will be using the cost data collected from rehabilitation centres and actual costs for the incentivised ORS to assess cost effectiveness. Incremental cost-effectiveness ratio (ICER) will be computed using the extra cost with incentives ($) / Improved uptake rate of rehabilitation with incentives (% attending at least one session).
Time Frame
3 months post-discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Diagnosed with stroke as defined by the World Health Organization's criteria; Discharged to home; Recommended by physicians to continue outpatient rehabilitation afte discharge; Singapore citizen or Permanent Resident; and Provision of informed consent. Exclusion Criteria: Stroke patients who are suffering from severe dysphasia without caregiver or proxy; Cognitively impaired patients without caregiver or proxy; and Age < 20 years.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David B Matchar, MD
Organizational Affiliation
Duke-NUS Graduate Medical School
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sherry Young, MD
Organizational Affiliation
Changi General Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Deidre A De Silva, MD
Organizational Affiliation
Singapore General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Changi General Hospital
City
Singapore
Country
Singapore

12. IPD Sharing Statement

Plan to Share IPD
No

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Stroke Patients' Outpatient Rehabilitation Therapy (SPORT)

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