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NCT Number: NCT06645639

Implementation of P-INPAC

The framework for Pediatric Integrated Nutrition Pathway for Acute Care (P-INPAC) was developed by the Canadian Malnutrition Task Force (CMTF); however, it has not been implemented in a research setting. The framework by CMTF for Integrated Nutrition Pathway for Acute Care (INPAC) in adults was also implemented in the "More-2-Eat" project which led to development of best practices in nutritional culture of the hospitals. Therefore, we intend to undertake this feasibility project at 3-sites to train staff and evaluate the implementation of P-INPAC components as part of routine healthcare procedure.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

30 day–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

McMaster Children's Hospital, Hamilton, Ontario, Canada

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About this study

The P-INPAC pilot study will be a 3-phase multi-center research study in hospitalized children, conducted at The Hospital for Sick Children, Toronto, and two other Canadian pediatric centres: Centre hospitalier universitaire Sainte-Justine, Montreal, Quebec and McMaster Children's Hospital, Hamilton, Ontario. P-INPAC is an algorithm which helps to identify, assess, and treat children with malnutrition.

In the first phase of the study, we will perform an audit of health records of all hospitalized patients at one selected study ward, one day of every other week for 8 weeks, at each of the 3 study sites to track their routine nutrition care. We anticipate auditing 80-100 patients/site in this cycle (total 240-300 patients). In addition, ≈12- 20 patients/ site (≈ 60 in total) who consent to detailed malnutrition screening and assessment would also be identified, assessed, and followed up one month after discharge. In addition, a questionnaire assessing the malnutrition knowledge, attitude, and self-perceived practices (KAP) amongst healthcare professionals will be conducted with staff, including trainees, at each site's study ward. Further, the workload of the study ward's Registered Dietitian (RD) will be assessed for 3 days.

In the second phase of the study, the health care team from each site's study ward will be trained by the site implementation research team about the P-INPAC, and how to administer nutritional screening and perform nutritional assessments, which is the Subjective Global Nutrition Assessment (SGNA).

Finally, in the third phase, we will monitor and evaluate the implementation of the first 2 steps of the P-INPAC (screening & assessment) over a period of 4 months assessing the acceptability, adoption, and coverage of improved nutrition care practices on the same pediatric study wards. We anticipate auditing 160-200 patients/site in this cycle (total 480-600 patients). In addition, detailed patient level data collection will take place in a selected group of consented patients, ≈24-40 patients per site from the 3 sites (≈120 in total). We would also follow-up with these patients a month after discharge.

Healthcare providers will be invited to answer the KAP questionnaire post-implementation version. We will compare responses from phase 1 with phase 3 (pre-/ post-follow up). And, the workload of the ward RD will be assessed again over 3 days.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Phase 1 and Phase 3 - Audited patient group inclusion Criteria:

  • ≥ 30 days of age and less than18 years of age on day of assessment
  • Anticipated Length of hospital stay ≥24 hours from day of assessment

Phase 1 & Phase 3 Detailed patient group inclusion Criteria:

  • Admitted to either a general medical or surgical ward
  • ≥ 30 days of age and less than 18 years of age on day of assessment
  • Anticipated Length of stay ≥ 24 hours from day of assessment
  • Speak English (or French at Quebec site) or have a family proxy available at the meal to provide information if first language of patient is not English (or French at Quebec site)
  • Patient/ caregiver provides written consent to participate

Exclusion criteria

a. Patients with eating disorder, somatization disorders, ARFID, FORM 1 etc. where the study interaction might interfere with the messaging or therapeutic plan as set out by the responsible team.

Phase 1 and 3 for Health Care Providers inclusion criteria:

  • Implied consent to participate by completing the KAP questionnaire
  • Providing clinical service for the select ward

Treatment and study plan

Pediatric Integrated Nutrition Pathway for Acute Care Pathway (P-INPAC)

Other

The pediatric working group of Canadian Malnutrition Task Force has developed an evidence-informed algorithm named the Pediatric Integrated Nutrition Pathway for Acute Care (P-INPAC). The P-INPAC outlines a process to improve nutrition care by:

  • implementing nutrition screening at point-of-admission
  • introducing standard care measures to prevent the development of malnutrition in children admitted with normal nutrition status, including standardizing the process of monitoring food intake early and systematically to identify when standard care measures are not sufficient
  • ensuring the moderately and severely malnourished patients receive timely specialized care in the form of a comprehensive assessment and treatment; and
  • ensuring moderately and severely malnourished patients receive adequate post discharge follow-up and nutrition care.

In this pilot study, we will be implementing the first two steps of P-INPAC only (screening and assessment).

Primary outcomes

  1. Baseline nutrition risk screening using STRONGkids or PNST

    Time frame: 2-month period (phase 1)

    Determine routine standard nutritional care practices related to nutrition risk screening in hospitalized children during phase 1 of study using a validated tool, such as, STRONGkids or PNST.

  2. Baseline nutrition risk screening using weight

    Time frame: 2-month period (phase 1)

    Determine routine standard nutritional care practices related to nutrition risk screening in hospitalized children during phase 1 of study using routine anthropometrics - weight

  3. Baseline nutrition risk screening using height or length

    Time frame: 2-month period (phase 1)

    Determine routine standard nutritional care practices related to nutrition risk screening in hospitalized children during phase 1 of study using routine anthropometrics - height or length in children under 2 years of age

  4. Baseline nutrition risk screening using head circumference

    Time frame: 2-month period (phase 1)

    Determine routine standard nutritional care practices related to nutrition risk screening in hospitalized children during phase 1 of study using routine anthropometrics - head circumference in children under 2 years of age

  5. Determine baseline knowledge among healthcare providers using the KAP questionnaire

    Time frame: 2-month period (phase 1)

    Determine baseline knowledge among healthcare providers on recognizing malnutrition and its management in hospitalized children, including perceived barriers and practices, using the KAP questionnaire

  6. Determine changes in knowledge among healthcare providers using the KAP questionnaire

    Time frame: 4-month period (phase 3)

    Determine changes in knowledge among healthcare providers on recognizing malnutrition and its management in hospitalized children in Phase 3, including perceived barriers and practices, using the KAP questionnaire after training was completed in phase 2

  7. Determine success with training and feasibility of nutrition risk screening in hospitalized children using STRONGkids and PNST

    Time frame: 4-month period (phase 3)

    Determine success with training and feasibility of implementing the P-INPAC framework by assessing changes in standard nutritional care practices related to nutrition risk screening in hospitalized children during phase 3 of study using a validated tool, such as, STRONGkids and PNST

  8. Determine success with training and feasibility of nutrition risk screening in hospitalized children using weight

    Time frame: 4-month period (phase 3)

    Determine success with training and feasibility of implementing the P-INPAC framework by assessing changes in standard nutritional care practices related to nutrition risk screening in hospitalized children during phase 3 of study using routine anthropometrics - weight

  9. Determine success with training and feasibility of nutrition risk screening in hospitalized children using height/ length

    Time frame: 4-month period (phase 3)

    Determine success with training and feasibility of implementing the P-INPAC framework by assessing changes in standard nutritional care practices related to nutrition risk screening in hospitalized children during phase 3 of study using routine anthropometrics - height or length in children under 2 years of age

  10. Determine success with training and feasibility of nutrition risk screening in hospitalized children using head circumference

    Time frame: 4-month period (phase 3)

    Determine success with training and feasibility of implementing the P-INPAC framework by assessing changes in standard nutritional care practices related to nutrition risk screening in hospitalized children during phase 3 of study using routine anthropometrics - head circumference in children under 2 years of age

Sponsors and collaborators

Lead sponsor

The Hospital for Sick Children

Other

Collaborators

  • McMaster Children's Hospital
  • St. Justine's Hospital

Registry information

Official study title

Towards Implementation of the Pediatric Integrated Nutrition Pathway for Acute Care Pathway (P-INPAC) - Pilot Study

Acronym: P-INPAC

Important dates

Study start
2023
Primary completion
2025
Study completion
2026
First posted
Oct 17, 2024
Registry last updated
Jun 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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