Effects of Oral Nutritional Supplements in Nursing Home Residents

Sponsor
University of Erlangen-Nürnberg Medical School (Other)
Overall Status
Completed
CT.gov ID
NCT01859416
Collaborator
Pfrimmer Nutricia GmbH, Erlangen , Germany (Industry)
87
1
2
18
4.8

Study Details

Study Description

Brief Summary

Although oral nutritional supplements (ONS) are known to be effective to treat malnutrition in older persons, evidence from nursing home populations including demented residents is rare, especially with regard to functionality and well-being. A known barrier for ONS use among older persons is the volume that needs to be consumed, resulting in low compliance and thus reduced effectiveness.

Thus, this study aimed to investigate the effects of a new, low volume, energy- and nutrient-dense ONS on nutritional status, functionality and quality of life of nursing home residents with malnutrition or at risk of malnutrition.

In 6 nursing homes in Nuremberg and Fuerth, Germany, a standardized screening was performed to identify all residents with malnutrition or at risk of malnutrition who might possibly benefit from nutritional intervention. All subjects with either a Mini Nutritional Assessment (MNA®) score below 24 points, BMI ≤22 kg/m², a low food intake according to the nurses' perception or weight loss of ≥5% in the last 3 or ≥10% in 6 months, respectively, were invited to participate and asked for informed consent.

Eligible residents with informed consent were randomly assigned to the intervention group (IG) which received two bottles of the ONS per day (250 mL, 600 kcal) in addition to usual nutritional care or to the control group (CG) which received usual nutritional care only.

Assessment of nutritional parameters included body weight, BMI, arm- and calf-circumference and Mini Nutritional Assessment (MNA). Cognitive status, depression, activities of daily living, handgrip strength, gait speed and quality of life were examined using standardized instruments and protocols. All measurements and tests were performed at baseline, after 12 and 24 weeks.

Compliance and tolerance were documented daily by nursing staff and regularly controlled by the study team.

Statistical analysis was performed following the intention-to-treat (ITT) approach including all residents originally assigned to either the IG or CG unless residents died during the study. A sample size calculation was performed with body weight as the primary outcome parameter (0.8 power to detect a significant difference p<0.05, two-sided) based on an estimated mean body weight 55 kg and a mean difference in body weight between the groups after 12 weeks of 1.5±2.2 kg comparable to results previously observed in this population. To detect a significant difference between IG and CG, 35 subjects were needed for each group. While sample size calculation aimed at ensuring adequate power to detect meaningful differences, the actual statistical analysis was of exploratory nature.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Oral nutritional supplement
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
87 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Effects of Oral Nutritional Supplements in Nursing Home Residents
Study Start Date :
Mar 1, 2009
Actual Primary Completion Date :
Jul 1, 2010
Actual Study Completion Date :
Sep 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: Oral nutritional supplement

2 * 125 mL low volume, energy and nutrient dense ONS per day (2 * 300 kcal) in addition to usual nutritional care

Dietary Supplement: Oral nutritional supplement

No Intervention: Control

Usual nutritional care

Outcome Measures

Primary Outcome Measures

  1. Body weight [12 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • nursing home resident

  • Mini Nutritional Assessment (MNA®) score <24 points or BMI ≤22 kg/m² or low food intake according to the nurses' perception or weight loss of ≥5% in the last 3 or ≥10% in 6 months

  • informed consent

Exclusion Criteria:
  • anticipated hospital stay (>1 week)

  • renal disease (dialysis)

  • end-stage disease

  • intolerance to ONS according to previous attempts to administer these

Contacts and Locations

Locations

Site City State Country Postal Code
1 Institute for Biomedicine of Aging, Universität Erlangen-Nürnberg Nürnberg Germany 90408

Sponsors and Collaborators

  • University of Erlangen-Nürnberg Medical School
  • Pfrimmer Nutricia GmbH, Erlangen , Germany

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Erlangen-Nürnberg Medical School
ClinicalTrials.gov Identifier:
NCT01859416
Other Study ID Numbers:
  • IBA-2013(1)
First Posted:
May 21, 2013
Last Update Posted:
May 21, 2013
Last Verified:
May 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 21, 2013