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Co-designed Nutritional Training Program for Oncology Nurses in Vietnam (NUTRI-NURSE-VN)

28 aprile 2026 aggiornato da: Phung Thi Hanh, VinUniversity

Effectiveness and Acceptability of a Co-Designed Nutritional Training Program for Oncology Nurses in Vietnam: A Single-Group Pre-Post Intervention Study

This study evaluates a co-designed nutritional training program for oncology nurses in Vietnam. The aim is to improve nurses' knowledge, confidence, and clinical practice in providing nutritional support for patients with cancer experiencing treatment-related symptoms.

The study used a single-group pre-post intervention design. Oncology nurses participated in a structured training program that included theoretical sessions and supervised clinical practice. After training, nurses delivered nutritional support to patients during routine care.

The study assessed changes in nurses' knowledge, self-confidence, and practice performance before and after the intervention. In addition, the acceptability of the program was evaluated from both nurses and patients who received the nutritional support.

This study provides preliminary evidence on the feasibility and potential effectiveness of a nurse-led nutritional training program and supports the integration of structured nutritional care into routine oncology practice.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

This study aimed to evaluate the effectiveness and acceptability of a co-designed nutritional training program for oncology nurses in Vietnam. The intervention was developed using a co-design approach involving patients, nurses, dietitians, and other healthcare professionals to ensure relevance, feasibility, and cultural appropriateness.

The study employed a single-group pre-post intervention design and was conducted at a tertiary teaching hospital in Vietnam. A convenience sample of oncology nurses participated in the training program. The intervention consisted of a three-day training workshop, including theoretical education on cancer-related nutrition and supervised clinical practice sessions. During the clinical component, nurses applied their knowledge in real patient interactions under supervision, using a structured checklist to guide nutritional assessment and counselling.

Following the training, nurses delivered nutritional support to patients with cancer experiencing treatment-related symptoms, including gastrointestinal and oral complications affecting dietary intake. The intervention focused on symptom-based dietary management strategies, practical counselling techniques, and patient-centered communication.

The primary outcomes were changes in nurses' knowledge and self-confidence in providing nutritional support, measured before and after the training program. Secondary outcomes included nurses' clinical practice performance, assessed using a standardized observational checklist, and the acceptability of the intervention among both nurses and patients.

Patient participants received nutritional support as part of routine care delivered by trained nurses. Acceptability was assessed one week after the intervention using a structured questionnaire to evaluate perceived usefulness, clarity, and applicability of the dietary guidance.

This study provides preliminary evidence on the feasibility, safety, and effectiveness of a nurse-led, co-designed nutritional training program. The findings support the role of oncology nurses in delivering structured nutritional care and highlight the potential for integrating such interventions into routine clinical practice, particularly in resource-constrained settings.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

20

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

  • Vietnam
    • Hanoi
      • Hanoi, Hanoi, Vietnam, 100000
        • Hanoi Medical University Hospital

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria:

  • Registered oncology nurses involved in direct patient care
  • Working in oncology departments at the study site
  • Willing to participate in the training program and evaluation

Exclusion Criteria:

  • Nurses not involved in direct patient care
  • Nurses unable to attend the full training program
  • Nurses who decline to participate

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Nutritional Training Program
Participants receive a co-designed nutritional training program consisting of a three-day workshop with theoretical education and supervised clinical practice. Following the training, oncology nurses apply the acquired knowledge and skills to provide nutritional support to cancer patients during routine care, using a structured checklist to guide assessment and counselling.
Comportamentale: Co-Designed Nutritional Training Program

The intervention is a co-designed nutritional training program for oncology nurses developed through stakeholder engagement, including patients and healthcare professionals. The program consists of a three-day workshop combining theoretical education and supervised clinical practice.

The training focuses on symptom-based nutritional management for cancer patients, including dietary strategies for common treatment-related symptoms such as nausea, diarrhoea, constipation, and oral complications. Nurses are trained to use a structured checklist to guide nutritional assessment, identify patient needs, and provide tailored counselling.

Following the training, nurses apply the acquired knowledge and skills during real patient interactions in routine clinical care, delivering individualized nutritional support based on patients' symptoms and conditions.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Nutritional Knowledge Score
Lasso di tempo: Baseline (pre-intervention) and 7 days post-intervention
Nutritional knowledge of oncology nurses measured using a 25-item structured questionnaire assessing knowledge of cancer-related nutrition and dietary management. Scores range from 0 to 50, with higher scores indicating greater knowledge.
Baseline (pre-intervention) and 7 days post-intervention
Change in Self-Confidence in Providing Nutritional Support
Lasso di tempo: Baseline (pre-intervention) and 7 days post-intervention
Self-reported confidence of oncology nurses measured using a 17-item Likert scale assessing confidence in delivering nutritional support for cancer-related symptoms. Each item is rated from 1 (not confident at all) to 5 (very confident), with higher scores indicating greater confidence.
Baseline (pre-intervention) and 7 days post-intervention

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Clinical Practice Performance Score
Lasso di tempo: Immediately post-intervention during supervised clinical practice
Nurses' competency in delivering nutritional support assessed using a standardized observational checklist during real patient interactions. The checklist includes 8 key tasks scored from 0 to 2, with total scores ranging from 0 to 16. Higher scores indicate better performance.
Immediately post-intervention during supervised clinical practice
Acceptability of the Training Program
Lasso di tempo: One week after intervention delivery
Acceptability of the intervention assessed among nurses and patients using the Intervention Rating Profile (IRP-15). The scale includes 15 items rated on a 6-point Likert scale, with higher scores indicating greater acceptability.
One week after intervention delivery

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

VinUniversity

Investigatori

  • Cattedra di studio: Lan Van Hoang, Dr, Phenikaa University

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

  • Phung TH, Nguyen TN, Hoang LV, Truong QT, Bradford N. Improving nurse-led nutritional support for patients with cancer: a protocol using co-design approach. Journal of Nursing Science. 2024.

Collegamenti utili

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 agosto 2024

Completamento primario (Effettivo)

30 agosto 2024

Completamento dello studio (Effettivo)

30 agosto 2024

Date di iscrizione allo studio

Primo inviato

28 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

28 aprile 2026

Primo Inserito (Effettivo)

4 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

4 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

28 aprile 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • VMEC-72-2024-NUTRI
  • 72/2024/QĐ-VMEC (Altro identificatore: Institutional Ethical Review Board for Biomedical Research of Vinmec International General Hospital JSC - VinUniversity)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Descrizione del piano IPD

Individual participant data (IPD) sharing has not yet been determined. Data sharing will be considered in accordance with institutional policies, ethical approvals, and participant confidentiality requirements.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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