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Completed

NCT Number: NCT03501290

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

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.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Toulouse University Hospital (CHU de Toulouse)

Toulouse, 31059, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

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.

Treatment and study plan

Fortimel® Protein supplementation

Dietary Supplement

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 outcomes

  1. Fortimel® compliance

    Time frame: At the end of the first month : Day 30

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

Secondary outcomes

  1. Fortimel® Compliance

    Time frame: Change at one and three months

    Fortimel® Compliance as defined as the consumption of at least 75% of the prescribed volume of ONS after 3 months supplementation,

  2. Body weight evolution

    Time frame: Change at one and three months

    Body weight evolution measured during the follow up visits at one month and three months,

  3. SPPB score

    Time frame: Change at one and three months

    Short Physical Performance Battery (SPPB) score (global score and each item)

  4. MNA

    Time frame: Change at one and three months

    MNA scores evolution

  5. ADL

    Time frame: Change at one and three months

    ADL scores evolution

  6. Fragility : Fried criteria

    Time frame: Change at one and three months

    Fragility : Fried criteria evolution

  7. EuroQoL

    Time frame: Change at one and three months

    EuroQoL scores evolution

  8. Nutritional history intake

    Time frame: Change at one and three months

    Nutritional history intake evolution

Sponsors and collaborators

Lead sponsor

University Hospital, Toulouse

Other

Collaborators

  • Nutricia, Inc.

Registry information

Acronym: OFraDDom

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Apr 18, 2018
Registry last updated
Aug 25, 2020

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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