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NCT Number: NCT06706661

Implementation of Nutritional Efforts on Discharged Older Patients

The aim of the study is to implement a nutritional treatment when discharging older patients at risk of malnutrition.

Data collected in the study will include an assessment of whether a combination of nutritional treatment and a liaison team reduces the risk of readmissions and mortality, improves nutritional status, physical function and quality of life

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Herlev and Gentofte Hospital

Herlev, 2730, Denmark

Location status: Recruiting

Location contact

Anne Marie Beck, Senior researcher

CONTACT

[email protected]

+45 38682387

Tina Munk

CONTACT

About this study

During hospitalization, many older patients are at risk of malnutrition. Malnutrition in older adults is related to reduced physical function, more complications, re-admissions, days in hospital and reduced quality of life. As hospitalizations are often short (approximately 5 days), it is important to focus on nutritional intake during the convalescence period.

Upon discharge, a "Nutrition Gap" often occurs in practice, where the patient does not consume sufficient nutrition to ensure an optimal convalescence period. The lack of nutritional follow-up in connection with the discharge of older patients has been shown to have a markedly negative effect on, among other things, functional ability and readmissions. A study from Herlev Hospital, where the effect of a nutritional treatment upon discharge of older patients was investigated, showed a significant effect on muscle strength, quality of life and nutritional status. Another study from Herlev Hospital has shown that by associating a clinical dietitian with a liaison team and thus focusing on nutrition, the readmission rate was halved.

The problem is that it has not been investigated whether such a cross-sectoral effort can be implemented in practice and the results confirmed.

Hypothesis 1 is that it is possible to include and retain the older patients who are discharged with the liaison team for an effort that includes treatment of the risk of malnutrition and that the older participants find the effort relevant

Hypothesis 2 is that nutritional treatment will be able to reduce the number of unintended readmissions and thereby be cost-effective. Furthermore, it is expected that the nutritional treatment will increase the participants' nutritional status, muscle strength, muscle mass, quality of life and possibly have a positive effect on mortality.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Prescription of the Liaison team At nutritional risk according to NRS2002 Age 50+ Can read, hear and understand Danish or English Cognitive able to participate in the study, based on whether they are informed in time, place and own data

Exclusion criteria

Receives enteral or parenteral nutrition Following a special diet including texture modified food and drinks Short life expectancy Not deemed eligible by the project staff

Treatment and study plan

Nutritional treatment

Other

At the day of discharge the intervention group (IG) receives a package containing foods and drinks covering dietary requirements for the next 24 h. Further, a goodie-bag containing samples of protein-rich milk-based drinks is provided. At day 4 after discharge, the IG receives dietetic counselling including a recommendation of daily exercise, and an individual nutrition plan. Information regarding recommendations of nutritional therapy after discharge is systematically and electronically communicated to the municipality. The dietician performes telephone follow-ups on day 30 and a home visit at 12 weeks

Primary outcomes

  1. Eligibility

    Time frame: Assessed at baseline

    Eligibility will be assessed as the number of patients who fulfil the inclusion criteria out of the number of patients discharged with the liaison team

  2. Recruitment

    Time frame: Assessed at baseline

    Recruitment rate will be assessed as the number of patients recruited out of the number of eligible patients

  3. Retention

    Time frame: Assessed at three months

    Retention rate will be assessed as the number of patients who complete the nutritional treatment out of the total number of patients recruited

Secondary outcomes

  1. Mortality

    Time frame: 30 days, 12 weeks, 6 monts, 1 year and 3 year

    health care records

  2. Hospital re-admissions

    Time frame: 30 days, 12 weeks, 6 monts, 1 year and 3 year

    health care records

  3. Health related Quality of life

    Time frame: 12 weeks

    Euro-qol tool EQ5D5L

  4. Appetite

    Time frame: 30 days, 12 weeks

    SNAQ with a score from 5 to 20 where a score at or below 14 can predict weight loss

  5. Muscle strenght

    Time frame: 4 days, 30 days, 12 weeks

    30 seconds chair stand

  6. Dietary intake

    Time frame: 30 days, 12 weeks

    24 hours recall

  7. weight

    Time frame: 4 days, 30 days

    body weight measurement

  8. muscle mass

    Time frame: 12 weeks

    calf circumference

Study contacts

Contact information is provided by the study sponsor or research team.

Anne Marie Beck, Ph.d.

CONTACT

+45 38682387

Tina Munk, Ph D

CONTACT

[email protected]

+45 61160138

Sponsors and collaborators

Lead sponsor

Herlev and Gentofte Hospital

Other

Registry information

Official study title

Implementation of Nutritional Treatment to Older Patients Discharged With the Liaison Team

Acronym: KMH2

Important dates

Study start
2025
Primary completion
2030
Study completion
2030
First posted
Nov 26, 2024
Registry last updated
Jul 7, 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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