1)What are the important design-, usability issues and recommendations when attempting to improve a prototype smartphone application for patient-reported pain outcomes? 2) What is the difference in pain intensity self reported by the patient and…
ID
Bron
Aandoening
Postoperative Pain, Pain management, Pain self registration, Pain app, smartphone appication testing
Ondersteuning
Oosterpark 9<br>
1091 AC Amsterdam<br>
The Netherlands<br>
Attention: J van Roon, MSc CEO
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WM de Hoop stichting: € 17.000,00
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1) Collecting feedback from patients, healthcare professionals and ICT technicians in order to improve the current prototype pain assessment tool, the PAIN app, and the bidirectional communication and ‘rapid response’ of ward nurses and the anaesthetic team. <br>
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2) Exploring the differences in reliability validity and the responsiveness between patient self reported pain intensity and the reported NRS by nurses in EMR
Achtergrond van het onderzoek
In this proof of concept study we will collect data of patients, healthcare professionals and ICT technician’s experiences on the usability and the validity of the application. The use of this application during the course of this study will have no clinical implications for the treatment of postoperative pain. Patients will receive care as usual provided by the ward nurses.
Doel van het onderzoek
1)What are the important design-, usability issues and recommendations when attempting to improve a prototype smartphone application for patient-reported pain outcomes?
2) What is the difference in pain intensity self reported by the patient and the reported NRS by nurses in HER?
Onderzoeksopzet
-start patient recruitment september 19th 2017
-end patient inclusion november 19th 2017
Onderzoeksproduct en/of interventie
Patients willing to participate in this study receive a smartphone application for self registration of postopoperative pain during their admission in hospital
Publiek
B. Thiel
Oosterparkstraat 9
Amsterdam 1091 AC
The Netherlands
+31 (0)20 59992512 (dect: 4773)
b.thiel@olvg.nl
Wetenschappelijk
B. Thiel
Oosterparkstraat 9
Amsterdam 1091 AC
The Netherlands
+31 (0)20 59992512 (dect: 4773)
b.thiel@olvg.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
All patients undergoing surgery are eligible for participation in this proof of concept. A patient must meet all of the following criteria: age 18 years or older, undergoing surgery and in possession of a smartphone and willing to participate in this proof of concept study.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
A patient who meets any of the following criteria will be excluded from participation in this study: age 0-18years, not able to use computer or smartphone, not able to read or understand Dutch.
Opzet
Deelname
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL6565 |
| NTR-old | NTR6746 |
| Ander register | : OLVG WO 17.103 |