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Decision Support System for Stroke Survivors (STARR)

B

Biocruces Bizkaia

Status

Unknown

Conditions

Telerehabilitation
Stroke
Life Style

Treatments

Device: eHealth Technologies

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

eHealth Technologies
Experimental group
Description:
eHealth Technologies is a messure of diferent paramenters of the patient; heart rate, blood pressure, weight, thermometer, daily activity.
Treatment:
Device: eHealth Technologies
Control
No Intervention group
Description:
Habitual treatment.

Trial contacts and locations

1

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Central trial contact

Leire Ortiz; Joana Sagastagoya

Data sourced from clinicaltrials.gov

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