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JOURNAL ONKOLOGIE – STUDIE

Mobile Health Technology for Palliative Care Patients

Rekrutierend

NCT-Nummer:
NCT03038841

Studienbeginn:
Februar 2017

Letztes Update:
21.06.2017

Wirkstoff:
-

Indikation (Clinical Trials):
Neoplasm Metastasis, Chronic Disease

Geschlecht:
Alle

Altersgruppe:
Erwachsene (18+)

Phase:
-

Sponsor:
University of Zurich

Collaborator:
Swiss Federal Institute of Technology, Swiss Academy of Medical Sciences (SAMS),

Studienleiter

Matthias Guckenberger, Prof
Study Chair
Clinic of Radiation-Oncology USZ
Gerhard Tröster, Prof
Study Chair
University of Zurich
Gudrun Theile, MD
Principal Investigator
Clinic of Radiation-Oncology USZ

Kontakt

Studienlocations
(1 von 1)

Clinic of Radiation-Oncology University Hospital Zurich
8091 Zürich
SwitzerlandRekrutierend» Google-Maps
Ansprechpartner:
Gudrun Theile, MD
Phone: +41 44 255 5495
E-Mail: gudrun.theile@usz.ch

Matea Pavic, MD
Phone: +41 44 255 3015
E-Mail: matea.pavic@usz.ch
» Ansprechpartner anzeigen

Studien-Informationen

Brief Summary:

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.

Ein-/Ausschlusskriterien

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.

Studien-Rationale

Primary outcome:

1. Feasibility (time of complete data transfer in weeks) (Time Frame - 12 weeks):
time of complete data transfer in weeks

Geprüfte Regime

  • Mobile Health:
    Patients discharged from hospital will be equipped with a tracking bracelet and a smart phone

Quelle: ClinicalTrials.gov


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