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Decision Support System for Stroke Survivors

Efficacy and Usability of eHealth Technologies in Stroke Survivors for Prevention of a New Stroke and Improvement of Self-management: Phase III Randomized Control Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03580642
Acronym
STARR
Enrollment
40
Registered
2018-07-09
Start date
2018-04-27
Completion date
2019-12-01
Last updated
2018-07-24

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

Conditions

Life Style, Stroke, Telerehabilitation

Brief summary

The aim of the study is to evaluate the usability of the system and its accordance with the users' needs. This evaluation will consider the effectiveness and the efficiency of the system, as well as stroke survivors' satisfaction. The effectiveness and the efficiency of the system will be measured by: * The relationship between the control of stroke survivors' daily activities and their risk of having a secondary stroke, * The decrease of the need for caregivers, * And consequently an improvement in stroke survivors' self-management.

Detailed description

The aim of the study is to evaluate the usability of the system and its accordance with the users' needs. This evaluation will consider the effectiveness and the efficiency of the system, as well as stroke survivors' satisfaction.

Interventions

DEVICEeHealth Technologies

The controls will get a conventional treatment from the acute to the chronic phase of stroke and the cases will get a conventional treatment till the end of the subacute phase. However, in the chronic period they will use the developed STARR App and DSS, as well as commercial wearables.

Sponsors

Biocruces Bizkaia Health Research Institute
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

We will perform a randomised, pilot, prospective, parallel group, open, and unicentric Clinical Trial (RCT) with stroke survivors and their caregivers at Cruces University Hospital.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 18 to 80 years. * First ischemic stroke within the past 6 months. * Hemiparesia with mild (91-99)-moderate (61-90) disability (Barthel Index). * With or without speech patology but able to understand simple orders ( \>45). * Able to cope and to understand the guidelines to use the devices. * Informed consent signed.

Exclusion criteria

* Life expectancy \<12 months. * Severe cognitive impairments. * Medical comorbidities that could interfere with the home-rehabilitation program (MoCA \< 26). * Socio-familiar dystocia (SFES ≥ 14). * Modified Rankin Scale \> 1.

Design outcomes

Primary

MeasureTime frameDescription
System Usability Scale12 monthsThe System Usability Scale (SUS) provides a quick and dirty, reliable tool for measuring the usability. Developers work to create systems that are easy and straight-forward for people to use. Terms such as user friendly and easy-to-use often indicate these characteristics, but the overall technical name for them is usability.

Secondary

MeasureTime frameDescription
Stroke date12 monthsThis an outcome to evaluate the eligibility of the patient. This variable will be the patient stroke date.
Oxfordshire Community Stroke Project Classification12 monthsThis an outcome to evaluate the eligibility of the patient. This variable will be useful in estimation of after stroke complications and prognostication.
Modified Barthel Index12 monthsThis an outcome to evaluate the eligibility of the patient. This variable will assessing self care and mobility activities of daily living of the patient.
Mississippi Aphasia Screening Test12 monthsThis an outcome to evaluate the eligibility of the patient. This variable will to be used to detect changes in language abilities over time of the patient.
Montreal Cognitive Assessment12 monthsThis an outcome to evaluate the eligibility of the patient. This variable will be collected for detecting cognitive impairment of the patient.
Gijon's social-familial evaluation Scale12 monthsAssess the social and family situation of people living in the home. Detect risk situations and social problems. There are no subscales. It has a global score. Score between 0-20 points, indicating higher score worse social situation.
Charlson Comorbidity Index12 monthsThis an outcome to evaluate the eligibility of the patient.
Gender12 monthsThis is a socio demographic outcome. This outcome will be collected as Male or Female.
Ethnic group12 monthsThis is a socio demographic outcome.
Deprivation index12 monthsThis is a socio demographic outcome.
Hand dominance12 monthsThis is a socio demographic outcome. This outcome will be collected as right-handed and left-handed.
Education level12 monthsThis is a socio demographic outcome.
Type of profession12 monthsThis is a socio demographic outcome.
Hobbies12 monthsThis is a socio demographic outcome.
Medical Research Council Scale12 monthsScale for testing muscle strength in palsy. There are no subscales. It measures from Grade 0 (No contraction) to Grade 5 (Normal strength).
MAST Test12 monthsThis is a neurological physical examination.
MoCA Test12 monthsThis is a neurological physical examination.
Functional Ambulation Categories12 monthsThis is a neurological physical examination.
10 Meters Walking Test12 monthsThis is a neurological physical examination. The variable will collected in m/sg.
6 Minutes Walking Test12 monthsThis is a neurological physical examination. The variable will collected in metres.
Berg Balance Scale12 monthsThis is a neurological physical examination.
Frenchay Arm Test12 monthsThis is a neurological physical examination.
Asworth Modified Scale12 monthsScale for testing muscle spasticity. It rates severity of tone. There are no subscales. It measures from Grade 0 (No increase in muscle tone) to Grade 4 (Affected part(s) rigid in flexion or extension).
Fatigue Severity Scale12 monthsTo measure the fatigue caused by a number of chronic medical conditions. There are no subscales. It has a global score. The FSS questionnaire contains nine statements. A low value (e.g., 1) indicates strong disagreement with the statement, whereas a high value (e.g., 7) indicates strong agreement. The total mean score is 7 points. FSS mean score \> 4 indicates severe fatigue.
Line Bisection Test12 monthsThis is a neurological physical examination.
Disphagia12 monthsThis is a neurological physical examination.
Campimetry12 monthsThis is a neurological physical examination.
Analogic Visual Scale12 monthsThis is a neurological physical examination.
Analgesic Treatments12 monthsThis is a neurological physical examination.
Golberg Scale12 monthsThis is a cardiovascular risk factor. To messure depression and anxiety.
Weight12 monthsThis is a cardiovascular risk factor. In kg
Height12 monthsThis is a cardiovascular risk factor. In meter
BMI12 monthsThis is a cardiovascular risk factor.
Waist Size12 monthsThis is a cardiovascular risk factor.
Waist to Hip Ratio12 monthsThis is a cardiovascular risk factor.
Blood Pressure12 monthsThis is a cardiovascular risk factor. In mmHg
Heart Rate12 monthsThis is a cardiovascular risk factor.
Glycaemia12 monthsThis is a cardiovascular risk factor.
Health Literacy Test12 monthsThis is for measure the health literacy of the patient.
Mediterranean Diet Assessment Test12 monthsThis is for measure the life style of the patient.
Physical Activity12 monthsThis is for measure the life style of the patient.
Toxic Consumption12 monthsThis is for measure the life style of the patient.
Total Cholesterol12 monthsThis is a blood test for measure the lipidic profile of the patient.
HDL12 monthsThis is a blood test for measure the lipidic profile of the patient.
LDL12 monthsThis is a blood test for measure the lipidic profile of the patient.
Proteins12 monthsThis is a blood test of the patient.
Albumin12 monthsThis is a blood test of the patient.
HbA1c12 monthsThis is a blood test of the patient.
Apoprotein B12 monthsThis is a blood test of the patient.
Apoportein A112 monthsThis is a blood test of the patient.
Lawton Index12 monthsThis is to messure the activities of daily living of the patient.
SF-3612 monthsThis is to messure the quality of life of the patient.
SIS12 monthsThis is to messure the quality of life of the patient.
Stroke Self Management Questionary12 monthsThis is to messure the self management satisfaction of the patient.
Age12 monthsThis an outcome to evaluate the eligibility of the patient. Age variable will be in years.
Satisfaction Questionary12 monthsThis is to messure the self management satisfaction of the patient.
Post Stroke Checklist12 monthsThis is to messure the adherence to the treatment of the patient.
Pharmacological Accountability12 monthsThis is to messure the adherence to the treatment of the patient.
Non Pharmacological Accountability12 monthsThis is to messure the adherence to the treatment of the patient.
Stroke Recurrences12 monthsThis is to messure the complications of the patient.
Number of Readmissions12 monthsThis is to messure the complications of the patient.
Stroke Management Questionary12 monthsThis is to messure the self management satisfaction of the patient.

Countries

Spain

Contacts

Primary ContactLeire Ortiz
LEIRE.ORTIZFERNANDEZ@osakidetza.eus+ 34 685779523
Backup ContactJoana Sagastagoya
JOANA.SAGASTAGOYAZABALA@osakidetza.eus+ 34 94 600 6000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026