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Compliance to Oral Nutritional Supplements (ONS) in Undernourished Frail Older Adults Living at Home. (OFraDDom)

Primary Purpose

Frail Elderly

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Fortimel® Protein supplementation
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Frail Elderly focused on measuring Frailty, Malnutrition, Older adults, Oral Nutritional Supplements, Compliance

Eligibility Criteria

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

Inclusion Criteria:

  • Community dwelling
  • Pre-frail or frail as defined by Fried criteria: at least a low score on one of the following:

    • Weight loss
    • Exhaustion
    • Physical Activity
    • Walk time
    • Grip strength
  • Undernutrition defined as at least one of the following criteria :

    • weight loss (≥ 5% in 1 month or ≥ 10% in 6 months),
    • BMI < 21 kg/m2
    • or global MNA <23.5
  • Informed consent
  • Willingness and ability to comply with the protocol, including:
  • Participation in study visits
  • Taking the study products every day
  • Ability to perform test for physical functioning and frailty status
  • Ability to understand and fill out questionnaires

Exclusion Criteria:

  • Dependency or loss of autonomy: ADL<4
  • Dementia
  • MMSE ≤ <20 if study partner, MMSE<22 if loss of study partner
  • Use of enteral nutrition
  • Major depression: Geriatric Depression Scale >8
  • Cancer with acute treatment (chemotherapy, radiotherapy)
  • Allergy to cow milk proteins
  • Galactosemia
  • Investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements.

Sites / Locations

  • Toulouse University Hospital (CHU de Toulouse)

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Oral Nutritional Supplement Group

Arm Description

All patients will be in one group, receiving the active product, Oral Nutritional Supplement with 'Fortimel® Protein supplementation'

Outcomes

Primary Outcome Measures

Fortimel® compliance
Fortimel® compliance as defined as the consumption of at least 75% of the prescribed volume of ONS.

Secondary Outcome Measures

Fortimel® Compliance
Fortimel® Compliance as defined as the consumption of at least 75% of the prescribed volume of ONS after 3 months supplementation,
Body weight evolution
Body weight evolution measured during the follow up visits at one month and three months,
SPPB score
Short Physical Performance Battery (SPPB) score (global score and each item)
MNA
MNA scores evolution
ADL
ADL scores evolution
Fragility : Fried criteria
Fragility : Fried criteria evolution
EuroQoL
EuroQoL scores evolution
Nutritional history intake
Nutritional history intake evolution

Full Information

First Posted
November 13, 2017
Last Updated
August 24, 2020
Sponsor
University Hospital, Toulouse
Collaborators
Nutricia, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT03501290
Brief Title
Compliance to Oral Nutritional Supplements (ONS) in Undernourished Frail Older Adults Living at Home.
Acronym
OFraDDom
Official Title
Compliance to Oral Nutritional Supplements (ONS) in Undernourished Frail Older Adults Living at Home.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
June 1, 2016 (Actual)
Primary Completion Date
December 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse
Collaborators
Nutricia, Inc.

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
In this study, patients are supposed to take Fortimel® Protein, an Oral Nutritional Supplement (ONS) recommended in case of malnutrition once daily during the study period. Three visits will be planned for each patient enrolled in the study (baseline visit, visits of follow-up at 4 weeks and 12 weeks). Phone calls will be regularly organized during one month or three months according to the duration of supplementation. The primary purpose of the OFraDDom study is to assess the compliance with ONS (respect by the patient of the physician's prescription) at the end of the first month. Data regarding the beneficial effects of ONS, or compliance with ONS in frail elderly population, are very limited. The study could complete knowledge about oral nutritional supplementation in the undernourished frail elderly people and help to demonstrate that oral nutritional supplements have benefits on nutritional status and physical performances in frail elderly people.
Detailed Description
For elderly with Protein Energy Malnutrition (PEM) or at nutritional risk, evidences support that Oral Nutritional Supplements (ONS) and dietary counselling can increase dietary intake and improve quality of life. However, data regarding the beneficial effects of ONS, or compliance with ONS in frail elderly population, are very limited. In their RCT, testing the effect of protein supplementation, Tieland and colleagues (7) showed an improvement of SPPB in frail older adults randomized to receive 15 g of supplemental protein daily for 24 weeks compared with the placebo group (p=0.02). Another recent RCT on the effect of a daily supplementation with protein and micronutrients for 12 weeks in 87 frail older adults (usual gait speed <0.6 m/s; MNA < 24) showed that Physical Functioning increased by 5.9% (1 point) in the intervention group, although no change was observed in the control group. SPPB remained stable in the intervention group, although it decreased by 12.5% (1 point) in controls (8). In this study, patients are supposed to take Fortimel® Protein, an ONS recommended in case of malnutrition once daily during the study period. Patients fulfilling eligibility criteria will be asked whether they are interested to participate in the study and receive Fortimel® protein. After informed consent, three visits will be planned for each patient enrolled in the study (baseline visit, visits of follow-up at 4 weeks and 12 weeks). Phone calls will be regularly organized during one month or three month according to the duration of supplementation to collect the compliance with ONS and coach patients. First prescription of the study product will be done for one month. Prescription will be repeated for 2 additional months only after the patient's nutritional status and its global health status, as well as tolerability and compliance to the ONS, were re-assessed during the first follow-up visit at one month. Data regarding the beneficial effects of ONS, or compliance with ONS in frail elderly population, are very limited. To complete knowledge about oral nutritional supplementation in the undernourished frail elderly people, study purpose is to assess Fortimel® Protein compliance to know if this supplementation is well accepted and what are factors which limit compliance. More, it could help to demonstrate that oral nutritional supplements have benefits on nutritional status and physical performances in frail elderly people.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Frail Elderly
Keywords
Frailty, Malnutrition, Older adults, Oral Nutritional Supplements, Compliance

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All patients will be in one group, receiving the product.
Masking
None (Open Label)
Allocation
N/A
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Oral Nutritional Supplement Group
Arm Type
Other
Arm Description
All patients will be in one group, receiving the active product, Oral Nutritional Supplement with 'Fortimel® Protein supplementation'
Intervention Type
Dietary Supplement
Intervention Name(s)
Fortimel® Protein supplementation
Intervention Description
Patients are supposed to take Fortimel® Protein once daily during the study period. The prescription is one unit a day. First prescription of the study product will be done for one month. Prescription will be repeated for 2 additional months only after the patient's nutritional status and its global health status, as well as tolerability and compliance to the ONS, were re-assessed during the first follow-up visit at one month.
Primary Outcome Measure Information:
Title
Fortimel® compliance
Description
Fortimel® compliance as defined as the consumption of at least 75% of the prescribed volume of ONS.
Time Frame
At the end of the first month : Day 30
Secondary Outcome Measure Information:
Title
Fortimel® Compliance
Description
Fortimel® Compliance as defined as the consumption of at least 75% of the prescribed volume of ONS after 3 months supplementation,
Time Frame
Change at one and three months
Title
Body weight evolution
Description
Body weight evolution measured during the follow up visits at one month and three months,
Time Frame
Change at one and three months
Title
SPPB score
Description
Short Physical Performance Battery (SPPB) score (global score and each item)
Time Frame
Change at one and three months
Title
MNA
Description
MNA scores evolution
Time Frame
Change at one and three months
Title
ADL
Description
ADL scores evolution
Time Frame
Change at one and three months
Title
Fragility : Fried criteria
Description
Fragility : Fried criteria evolution
Time Frame
Change at one and three months
Title
EuroQoL
Description
EuroQoL scores evolution
Time Frame
Change at one and three months
Title
Nutritional history intake
Description
Nutritional history intake evolution
Time Frame
Change at one and three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Community dwelling Pre-frail or frail as defined by Fried criteria: at least a low score on one of the following: Weight loss Exhaustion Physical Activity Walk time Grip strength Undernutrition defined as at least one of the following criteria : weight loss (≥ 5% in 1 month or ≥ 10% in 6 months), BMI < 21 kg/m2 or global MNA <23.5 Informed consent Willingness and ability to comply with the protocol, including: Participation in study visits Taking the study products every day Ability to perform test for physical functioning and frailty status Ability to understand and fill out questionnaires Exclusion Criteria: Dependency or loss of autonomy: ADL<4 Dementia MMSE ≤ <20 if study partner, MMSE<22 if loss of study partner Use of enteral nutrition Major depression: Geriatric Depression Scale >8 Cancer with acute treatment (chemotherapy, radiotherapy) Allergy to cow milk proteins Galactosemia Investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne GHISOLFI, MD
Organizational Affiliation
Gérontopôle, CHU Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Toulouse University Hospital (CHU de Toulouse)
City
Toulouse
ZIP/Postal Code
31059
Country
France

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Compliance to Oral Nutritional Supplements (ONS) in Undernourished Frail Older Adults Living at Home.

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