Mobile Health Technology for Palliative Care Patients

NCT ID: NCT03038841

Last Updated: 2017-06-21

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

UNKNOWN

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-02-01

Study Completion Date

2018-05-31

Brief Summary

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To test the potential and acceptance of wireless activity tracking in palliative care patients leaving hospital care. Explorative study, collaboration project of the Clinic of Radiation-Oncology, University Hospital Zurich and the Wearable Computing Laboratory, Swiss Federal Institut of Technology. Patients receive a tracking bracelet and a smart phone in order to gather objective physical activity parameters as step count, sleep duration, heart rate, social activity patterns (e.g. making calls) as well as subjective ratings of pain and distress. Quality of life (QoL) will be captured by paper questionnaire. Correlations between patients' physical activity patterns and the pain and distress level assessed from electronic scales as well as QoL-questionnaire will be performed. Acceptance will be evaluated by quantitative questionnaires and interviews. The proposed study is meant to be preparatory work for an intervention study to test the effect of wireless monitoring of palliative care patients on fostering early interventions for symptom relief and support of QoL.

Detailed Description

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Conditions

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Metastatic Cancer Mobile Health Chronic Disease

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Interventions

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Mobile Health

Patients discharged from hospital will be equipped with a tracking bracelet and a smart phone

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* established diagnosis of metastatic cancer or other severe illness with limited life-expectancy (physicians guess \<12 months, \> 8 weeks)
* Karnofsky Index ≥50%
* ECOG≤ 2
* aged \> 18 years
* passed a short handling test with devices (tracking bracelet, smart phone)

Exclusion Criteria

* relevant cognitive impairment
* insufficient knowledge of German language.
Minimum Eligible Age

18 Years

Maximum Eligible Age

105 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Swiss Federal Institute of Technology

OTHER

Sponsor Role collaborator

Swiss Academy of Medical Sciences (SAMS)

OTHER

Sponsor Role collaborator

University of Zurich

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Matthias Guckenberger, Prof

Role: STUDY_CHAIR

Clinic of Radiation-Oncology USZ

Gerhard Tröster, Prof

Role: STUDY_CHAIR

ETH Zürich

Gudrun Theile, MD

Role: PRINCIPAL_INVESTIGATOR

Clinic of Radiation-Oncology USZ

Locations

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Clinic of Radiation-Oncology University Hospital Zurich

Zurich, Canton of Zurich, Switzerland

Site Status RECRUITING

Countries

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Switzerland

Central Contacts

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Gudrun Theile, MD

Role: CONTACT

+41 44 255 5495

Matea Pavic, MD

Role: CONTACT

+41 44 255 3015

Facility Contacts

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Gudrun Theile, MD

Role: primary

+41 44 255 5495

Matea Pavic, MD

Role: backup

+41 44 255 3015

Other Identifiers

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PC 16/16

Identifier Type: -

Identifier Source: org_study_id

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