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Published on: August 1, 2019
Pilot Testing of a Nurse-Led Basic Symptom Self-management Support for Patients Receiving First-Line Systemic
Marika Bana1, Karin Ribi, Solange Peters
1Author affiliations: School of Health Sciences, University of Applied Sciences and Arts Western Switzerland-Fribourg (Dr Bana); Institute of Higher Education and Research in Health Care IUFRS, University of Lausanne and Lausanne University Hospital, Faculty of Biology and Medicine (Drs Bana, Ribi, and Eicher); International Breast Cancer Study Group (Dr Ribi); Hospital Group Lindenhof, Bern (Mmes Kropf-Staub and Zürcher-Florin); Department of Practice Development in Nursing, Solothurner Spitäler (Mr Näf); Departement Onkologie/Hämatologie Kantonsspital Graubünden, Chur (Mrs Stoffel); Gynäkologisches Tumorzentrum, Universitätsspital Basel (Dr Bläuer); Brustzentrum Bern, Oncocare (Dr Borner); rundum Onkologie am Bahnhofplatz, Sargans (Mrs Malin); Tumorzentrum ZeTuP Rapperswil-Jona (Mrs Biber); freiburger spital HFR (Dr Betticher); Onkologie- und Hämatologiezentrum Thun-Berner Oberland (Mrs Kuhn-Bächler); Division Onkologie, Hämatologie und Transfusionsmedizin, Kantonsspital Aarau (Dr Cantoni and Mr Seeger); Universität Bern, CTU (Dr Butikofer); and Department of Oncology, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne (Drs Peters and Eicher), Switzerland.
The Symptom Navi Program (SNP) did not improve cancer patient symptom management in a pilot study. Further research is needed to refine the intervention for better patient outcomes.
Area of Science:
- Oncology Nursing
- Symptom Management
- Clinical Trial Design
Background:
- The Symptom Navi Program (SNP) is a nurse-led intervention designed for basic symptom self-management in cancer patients.
- The program has shown acceptance among both patients and healthcare professionals.
Purpose of the Study:
- To pilot the Symptom Navi Program (SNP).
- To evaluate patient-reported symptom outcomes, nursing support for symptom management, and patient safety.
- To assess the feasibility and potential efficacy of the SNP in a real-world setting.
Main Methods:
- A cluster-randomized design was employed, randomizing centers to either the SNP intervention or usual care.
- Adult patients initiating first-line systemic cancer treatment were included in the study.
- Primary outcome: change in symptom interference with daily functions; Secondary outcomes: symptom severity, burden, self-efficacy, perceived support, and patient safety.
Main Results:
- No significant differences were observed in symptom interference with daily functions between the SNP and control groups at 16 weeks.
- Secondary outcomes, including symptom severity, burden, self-efficacy, and perceived support, also showed no significant differences between groups.
- No adverse events were reported during the study, indicating patient safety.
Conclusions:
- Preliminary findings suggest the SNP did not significantly impact patient-reported symptom outcomes, self-efficacy, or symptom management support.
- Potential reasons for the lack of observed effect include inadequate statistical power and specific SNP components, such as insufficient training and limited follow-up consultations.
- The study highlights the need to reconsider the SNP's training content and intervention procedures to enhance its effectiveness.
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