A Dietitian-Driven Unified Nutritional Care Model (ADDUCE)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGødstrup Hospital

About this trial

The goal of this clinical trial is to learn whether a new way of organising hospital nutrition care can improve outcomes for adults who are admitted to medical wards and are at risk of malnutrition.

The main questions it aims to answer are:

* Does having clinical dietitians take primary responsibility for nutrition care shorten hospital stay? * Does this approach improve nutritional intake, nutritional status, quality of life, and patient satisfaction? * Does this approach lower healthcare costs compared with current practice?

Researchers will compare the new nutrition care model with current practice. In current practice, nursing staff are mainly responsible for nutrition screening and nutrition care planning, while clinical dietitians are involved only when requested. In the new model, clinical dietitians are part of the ward team and take primary responsibility for identifying patients at nutritional risk, planning nutritional care, and providing nutritional treatment.

Participants will:

* Receive either the current nutrition care approach or the new dietitian-led nutrition care approach, depending on when they are admitted to the ward * Complete questionnaires about their nutritional status, quality of life, and daily activities during their hospital stay and about 30 days later * Have information collected during their hospital stay and from their medical records, including nutritional intake, body weight, length of hospital stay, hospital readmissions, and other health outcomes

The study will be conducted on three medical wards at Gødstrup Hospital. All wards will start with current practice and will gradually change to the new nutrition care model during the study period. Researchers will compare outcomes before and after the new model is introduced.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years or older

Admitted to a participating medical ward during the study period

First eligible admission during the study period

Age 18 years or older

Disqualifiers

Terminally ill patients with short expected survival

Patients admitted to an isolation room at the time of recruitment

Trial design

Design model

Parallel

Treatments tested in this trial

  • Dietitian-driven nutritional care model

    Behavioral

    Clinical dietitians are integrated into the ward team and assume primary responsibility for systematic nutritional risk screening, nutritional assessment, nutritional care planning, follow-up, and nutritional treatment. Dietitians identify patients requiring nutritional care without waiting for referral and collaborate with nursing staff and other clinicians to provide coordinated nutritional care during hospital admission.

  • Current practice nutritional care

    Other intervention

    Nutritional care delivered according to existing ward procedures, with nursing staff primarily responsible for nutritional risk screening and nutritional care planning and clinical dietitians involved following referral or consultation.

Treatment groups

216 Participants
are divided into 2 treatment groups
Group A: Dietitian-driven nutritional care modelExperimental treatment 1 intervention
Group B: Current practiceActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Length of hospital stay

Length of hospital stay, defined as the time from hospital admission to hospital discharge. Length of stay will be calculated in hours from electronic health record time stamps and expressed in days (hours/24). Assessed using routinely collected hospital data from all eligible patients admitted to participating wards during the study period.

Time frame
Through study completion, an average of 5 days
2

Hospital re-admissions

Number of hospital readmissions after discharge from the index admission, assessed using routinely collected hospital data from all eligible patients admitted to participating wards during the study period.

Time frame
30 days, 90 days

Secondary outcomes

1

Days alive and out of hospital

Days alive and out of hospital after index admission. Assessed using routinely collected hospital data from all eligible patients admitted to participating wards during the study period.

Time frame
30 days, 90 days
2

Mortality

Assessed using routinely collected hospital data from all eligible patients admitted to participating wards during the study period.

Time frame
30 days, 90 days
3

Daily energy intake

Energy intake (kJ/day) expressed as a percentage of estimated energy requirements, assessed in the prospectively recruited cohort of approximately 216 enrolled participants. Energy intake will be estimated using a 24-hour dietary recall conducted as a structured interview with the participant, supported by data from the hospital electronic meal ordering system and the electronic administration records for enteral and parenteral nutrition.

Time frame
Day 1-3
4

Daily protein intake

Protein intake (g/day) expressed as a percentage of estimated protein requirements, assessed in the prospectively recruited cohort of approximately 216 enrolled participants. Protein intake will be estimated using a 24-hour dietary recall conducted as a structured interview with the participant, supported by data from the hospital electronic meal ordering system and the electronic administration records for enteral and parenteral nutrition.

Time frame
Day 1-3

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Gødstrup Hospital

Lead sponsor

The Danish Dietetic Association

Collaborator

NIDO Research Foundation

Collaborator

Health Research Foundation of Central Denmark Region

Collaborator