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Nutritional Intervention in Geriatric Patients

A Multidisciplinary Nutritional Intervention Programme Across Sectors to Improve the Nutritional Status of Geriatric Patients at Nutritional Risk - A Randomized Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03131856
Enrollment
150
Registered
2017-04-27
Start date
2012-10-15
Completion date
2015-12-31
Last updated
2017-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malnutrition

Keywords

Geriatrics, Nutritional risk, Multi-disciplinary intervention, Randomized Controlled Trial

Brief summary

This study aims to investigate the effect of a multi-disciplinary nutritional intervention program in geriatric nutritional at risk patients. The study is carried out as randomized controlled trial. The intervention consists of an individual dietary plan conducted by a clinical dietician before discharge in combination with three follow-up visits after discharge (1, 4 and 8 weeks).

Interventions

BEHAVIORALNutritional intervention programme

The intervention consisted of an individual dietary plan conducted by a clinical dietician before discharge in combination with three follow-up visits after discharge (1, 4 and 8 weeks) conducted by a district nurse.

Sponsors

University Hospital, Gentofte, Copenhagen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Eligible patients were randomized to either the intervention group or control group.

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 65 or above * BMI \<20.5 and/or weight loss within the last 3 months and/or a reduced dietary intake in the previous week and/or severely ill

Exclusion criteria

* Terminal illness * Active cancer diagnosis * Permanently living in a nursing home * Not willing or able to give an informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Nutritional statusThree months follow-upChange in body weight (kg)

Secondary

MeasureTime frameDescription
Functional statusThree months follow-upBarthel Index (scale 0-100)
Self-rated healthThree months follow-upSelf-rated health was measured with one single question with 5 possible responses on a Likert scale: In general, how would you rate your Health?
Re-admissionUp to three monthsAll-cause unplanned readmissions
Mortality1) Up to 90 days after discharge 2) Up to 120 days after dischargeAll-cause mortality

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026