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Quantifying Digital Behavior on Smart Phones - Data From Stroke Survivors

NCT ID: NCT04405635

Last Updated: 2023-12-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-30

Study Completion Date

2024-08-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Stroke

Keywords

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Stroke, digital behavior, health-related quality of life, cognitive function

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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No intervention or exposure

No intervention or exposure

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Leiden University

OTHER

Sponsor Role collaborator

Carlsberg Foundation

UNKNOWN

Sponsor Role collaborator

University of Aarhus

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Iris C. Brunner, PhD

Role: PRINCIPAL_INVESTIGATOR

Aarhus University, Hammel Neurocenter

Locations

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Hammel Neurorehabilitation Centre and University Research Clinic

Hammel, Aarhus, Denmark

Site Status RECRUITING

Countries

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Denmark

Central Contacts

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Iris Brunner, PhD

Role: CONTACT

Phone: +4560568195

Email: [email protected]

Jørgen Feldbæk Nielsen, PhD

Role: CONTACT

Facility Contacts

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Iris Brunner, PhD

Role: primary

Other Identifiers

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614731

Identifier Type: -

Identifier Source: org_study_id