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Effect of Nutritional Supplementation on Nutritional Status & Rehospitalization in Malnourished Elderly Patients

Primary Purpose

Malnutrition

Status
Active
Phase
Not Applicable
Locations
Indonesia
Study Type
Interventional
Intervention
Nutrient-dense drink
Sponsored by
Indonesia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malnutrition focused on measuring Malnutrition, Geriatric, Oral nutritional supplement

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: older patients (60-years or older) Malnourished or at risk of malnourished (based on Mini Nutritional Assessment score) Exclusion Criteria: Impaired kidney function (eGFR less than 30 ml/min/1.73 m2) Unwillingness to participate

Sites / Locations

  • Cipto Mangunkusumo National Hospital
  • Comprehensive Geriatric Clinic, Cipto Mangunkusumo Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Nutrient Dense Drink

Standard Care

Arm Description

Experimental: Nutrient-dense drink Nutrient-dense drink on top of standard care 200 kcal 15 grams of (whey) protein, 8 grams of fat, and 17 grams of carbohydrates including only 0.2 g lactose 400 IU vitamin D, 250 mg Ca, 10-20 % of the other vitamins/minerals Servings : • 100 ml water for dissolving 46 g of the served powder

Standard care comprising: Standard care only will be provided nutritional counseling to achieve a better nutritional state

Outcomes

Primary Outcome Measures

Changes of Energy in Kilocalories
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Changes in Protein intake in grams
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Changes in Fat intake in grams
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Changes in carbohydrate intake in grams
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Changes in micronutrients intake in micrograms
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)

Secondary Outcome Measures

Changes of Mini Nutritional Status Score
The nutritional status will be measured by full form mini nutritional assessment, individuals can be divided in 3 groups using threshold values of <17 for malnourished, 17-23,5 for at risk of malnutrition and ≥ 24 for normal nutritional status with a maximum total score of 30 points
Changes of Vitamin D level
Vitamin D level as a parameter of nutritional status will be measured by the direct competitive chemiluminescence microparticle immunoassay (CMIA) method
Changes of Body Weight
Body weight will be measured in the fasted state to the nearest 0.1 kg with a calibrated digital scale
Changes of Lean Body Mass
Lean body mass will be measured by Bioelectrical Impedance Analysis (BIA)
Changes of Short Physical Performance Battery Score
Physical performance will be measured by Short Physical Performance Battery as well as individual gait speed in second. The score is, If time is more than 6''52 sec : 1 point If time is 4"66 to 6"52 sec : 2 points If time is 3"62 to 4"65 sec: 3 points If time is less than 3"62 sec:4 points Balance Test in second Scoring Held for 10 sec : 1 point Not held for 10 sec : 0 points Not attempted :0 points If 0 points, and Balance Tests Participant unable to complete 5 chair stands or completes stands in >60 sec : 0 points If chair stand time is 16"70 sec or more: 1 points If chair stand time is 13"70 to 16"69 sec: 2 points If chair stand time is 11"20 to 13"69 sec: 3 points If chair stand time is 11"19 sec or less: 4 points Scoring for complete Short Physical Performance Battery Category Scores : 0 - 6 points : poor performance 7-9 points : moderate performance 10-12 points : good performances
Changes of Handgrip Strength
Handgrip strength will be measured by a handgrip dynamometer
Number of the Participants with Rehospitalization
Non-elective hospitalization will be recorded by medical history

Full Information

First Posted
March 9, 2022
Last Updated
September 28, 2023
Sponsor
Indonesia University
Collaborators
Wageningen University, FrieslandCampina
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1. Study Identification

Unique Protocol Identification Number
NCT06068816
Brief Title
Effect of Nutritional Supplementation on Nutritional Status & Rehospitalization in Malnourished Elderly Patients
Official Title
The Effect of 12 Weeks of Nutritional Supplementation on Nutritional Intake and Status in Older Outpatients With Malnutrition Risk
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 5, 2022 (Actual)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indonesia University
Collaborators
Wageningen University, FrieslandCampina

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary outcome is the mean difference in energy and protein as well as a selection of micronutrients (calcium, vitamin D, and Vitamin B12) after 12 weeks of intervention between standard care plus nutritional supplementation vs standard care. The secondary outcomes are body weight, nutritional status, body composition, physical performance, vitamin D level, and nonelective hospitalization The Study Hypothesize: The hypothesize that outpatients who receive nutrient-dense drinks (NDD) will have increased body weight, better nutritional status, better body composition, higher vitamin D level, better physical performance and reduced non-elective hospitalization than those receiving standard care after 12 weeks of intervention.
Detailed Description
Study Design: Randomized Controlled Trial, Randomized and controlled intervention trial with 2 treatments in parallel Treatment 1: nutrient-dense drinks on top of standard care Treatment 2: standard care only (reference) Location and time study: Geriatric outpatient clinic and internal medicine outpatient clinic in Cipto Mangunkusumo National Hospital Jakarta. The study will be conducted on July 2022 to October 2023. Study subject: elderly outpatients (aged 60 years old or more) who visit outpatient clinics will be screened for their eligibility as participants of this study. Sample Size: sample size for each group is 41 participants per group (for two groups a total of 82 participants). To anticipate a dropout of 20% a minimum of 98 participants (rounded to 100 participants in total) is the minimum sample size of our study. Data collection : Energy and nutrient intake, particularly protein calcium, vitamin D, and vitamin B12, Nutritional status based on full form Mini Nutritional Assessment, Vitamin D level, lean body mass (using Bioelectrical Impedance Analysis), physical performance will be measured by Shor Physical Performance Battery, handgrip strength, medical history, data on the demographic status and clinical data will be retrieved from the medical record and the attending physicians, body weight and anthropometric measurements, intervention: Nutrient Dense-Drink + Standard Care

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition
Keywords
Malnutrition, Geriatric, Oral nutritional supplement

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Subjects will be randomized to the treatment. Subjects will receive either standard care or standard care plus nutrients dense drinks. Randomization will be done by a third party who is not involved in the study.
Masking
Outcomes Assessor
Masking Description
Outcomes assessment will be performed by blinded raters.
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nutrient Dense Drink
Arm Type
Experimental
Arm Description
Experimental: Nutrient-dense drink Nutrient-dense drink on top of standard care 200 kcal 15 grams of (whey) protein, 8 grams of fat, and 17 grams of carbohydrates including only 0.2 g lactose 400 IU vitamin D, 250 mg Ca, 10-20 % of the other vitamins/minerals Servings : • 100 ml water for dissolving 46 g of the served powder
Arm Title
Standard Care
Arm Type
No Intervention
Arm Description
Standard care comprising: Standard care only will be provided nutritional counseling to achieve a better nutritional state
Intervention Type
Dietary Supplement
Intervention Name(s)
Nutrient-dense drink
Intervention Description
a nutrient-dense drink developed by FrieslandCampina in line with the European Society for Clinical Nutrition and Metabolism guidelines for the dietary management of older malnourished patients
Primary Outcome Measure Information:
Title
Changes of Energy in Kilocalories
Description
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Time Frame
at baseline, week 6, and week 12
Title
Changes in Protein intake in grams
Description
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Time Frame
at baseline, week 6, and week 12
Title
Changes in Fat intake in grams
Description
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Time Frame
at baseline, week 6, and week 12
Title
Changes in carbohydrate intake in grams
Description
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Time Frame
at baseline, week 6, and week 12
Title
Changes in micronutrients intake in micrograms
Description
Dietary intake will be measured using 3-day dietary food records, 2 weekdays and 1 weekend day)
Time Frame
at baseline, week 6, and week 12
Secondary Outcome Measure Information:
Title
Changes of Mini Nutritional Status Score
Description
The nutritional status will be measured by full form mini nutritional assessment, individuals can be divided in 3 groups using threshold values of <17 for malnourished, 17-23,5 for at risk of malnutrition and ≥ 24 for normal nutritional status with a maximum total score of 30 points
Time Frame
at screening (Week 0) and week 12
Title
Changes of Vitamin D level
Description
Vitamin D level as a parameter of nutritional status will be measured by the direct competitive chemiluminescence microparticle immunoassay (CMIA) method
Time Frame
Screening (Week 0) and week 12
Title
Changes of Body Weight
Description
Body weight will be measured in the fasted state to the nearest 0.1 kg with a calibrated digital scale
Time Frame
Screening (week 0), Week 4, Week 6, Week 12
Title
Changes of Lean Body Mass
Description
Lean body mass will be measured by Bioelectrical Impedance Analysis (BIA)
Time Frame
Screening (Week 0) and week 12
Title
Changes of Short Physical Performance Battery Score
Description
Physical performance will be measured by Short Physical Performance Battery as well as individual gait speed in second. The score is, If time is more than 6''52 sec : 1 point If time is 4"66 to 6"52 sec : 2 points If time is 3"62 to 4"65 sec: 3 points If time is less than 3"62 sec:4 points Balance Test in second Scoring Held for 10 sec : 1 point Not held for 10 sec : 0 points Not attempted :0 points If 0 points, and Balance Tests Participant unable to complete 5 chair stands or completes stands in >60 sec : 0 points If chair stand time is 16"70 sec or more: 1 points If chair stand time is 13"70 to 16"69 sec: 2 points If chair stand time is 11"20 to 13"69 sec: 3 points If chair stand time is 11"19 sec or less: 4 points Scoring for complete Short Physical Performance Battery Category Scores : 0 - 6 points : poor performance 7-9 points : moderate performance 10-12 points : good performances
Time Frame
Screening (Week 0) and week 12
Title
Changes of Handgrip Strength
Description
Handgrip strength will be measured by a handgrip dynamometer
Time Frame
Screening (Week 0) and week 12
Title
Number of the Participants with Rehospitalization
Description
Non-elective hospitalization will be recorded by medical history
Time Frame
3 months (12 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: older patients (60-years or older) Malnourished or at risk of malnourished (based on Mini Nutritional Assessment score) Exclusion Criteria: Impaired kidney function (eGFR less than 30 ml/min/1.73 m2) Unwillingness to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prof. Siti Setiati, MD (Internist Geriatrician),PhD
Organizational Affiliation
Indonesia University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Prof.Dr.Ing. Lisette CPGM de Groot, PhD
Organizational Affiliation
Wageningen University the Netherlands
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Rina Agustina, MD, PhD
Organizational Affiliation
Indonesia University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Esthika Dewiasty, MD (Internist Geriatrician), MSc
Organizational Affiliation
Universitas Indonesia, PhD candidate at Wageningen University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Sjors Verlaan, PhD
Organizational Affiliation
FrieslandCampina
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Rahmi Istanti, BSc, MPH
Organizational Affiliation
Indonesia University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Grace Wangge, MD, PhD
Organizational Affiliation
Monash University Indonesia
Official's Role
Study Director
Facility Information:
Facility Name
Cipto Mangunkusumo National Hospital
City
Jakarta
ZIP/Postal Code
10430
Country
Indonesia
Facility Name
Comprehensive Geriatric Clinic, Cipto Mangunkusumo Hospital
City
Jakarta
Country
Indonesia

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
All findings of this study will be published in an international open-access journal. Please contact us if any researchers need our individual participant data.

Learn more about this trial

Effect of Nutritional Supplementation on Nutritional Status & Rehospitalization in Malnourished Elderly Patients

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