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Quantifying Digital Behavior on Smart Phones - Data From Stroke Survivors (QuantStroke)

University of Aarhus logo

University of Aarhus

Status

Enrolling

Conditions

Stroke

Treatments

Other: No intervention or exposure

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

In this study, we want to continuously record the interaction of 50 stroke survivors with their smartphones during the first 3 months after discharge. The linkage of smart phone use to function and quality of life will be assessed with standardized outcome measures at defined time points.

Full description

People with stroke are among the most relevant target groups for unobtrusive monitoring. Worldwide, stroke is the second most frequent cause for lasting disability and causes a substantial burden for the individual, caregivers and society. Thanks to improved treatment, many stroke survivors can be discharged to their homes. However, many have to live with disabilities and are prone to declining function, cognitive impairment and depression. With the acquired data, we want to create a database where digital behavior is analyzed with advanced computational methods. In collaboration with the Department of Cognitive Psychology, University of Leiden, Netherlands, these data will be used to discover specific features for different health issues and to develop tools for the early detection of functional decline for different populations.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • New or recurrent stroke, admitted to rehabilitation, discharge to own home
  • Owns an Android smart phone
  • Smart phone is used by the patient only

Exclusion criteria

  • Severe cognitive impairments and / or psychiatric and behavioral conditions that interfere with compliance.
  • Not able to provide informed consent
  • Discharge to nursing homes or other care facilities

Trial contacts and locations

1

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Central trial contact

Jørgen Feldbæk Nielsen, PhD; Iris Brunner, PhD

Data sourced from clinicaltrials.gov

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