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Trial Radar IA
Lo studio clinico NCT05608707 per Perdita di appetito, Inattività fisica, Malnutrizione, Anorexia of Aging, Invecchiamento, Invecchiamento sano è attivo, non in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui.
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APPETITE: Plant Protein and Exercise Solutions for the Prevention of Undernutrition in Older Adults.

Attivo, non in arruolamento
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT05608707 è uno studio interventistico per Perdita di appetito, Inattività fisica, Malnutrizione, Anorexia of Aging, Invecchiamento, Invecchiamento sano, attualmente attivo, non in arruolamento. Avviato il 22 settembre 2022, prevede di arruolare 180 partecipanti. Sotto la guida di University College Dublin, dovrebbe concludersi entro il 1 settembre 2025. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 9 dicembre 2024.
Sommario breve
The APPETITE Trial aims to investigate the efficacy of innovative plant protein fibre (PPF) products (developed in a previous workpackage) as part of a personalised diet with/out physical activity on appetite and incidence of undernutrition in older persons from three European countries at high risk of undernutrition.
Descrizione dettagliata
It is normal that dietary intake decreases as we age due to reduced activity and muscle mass. However, appetite is a key determinant of dietary intake, and poor appetite can result in undernutrition. In many instances, older adults do not recognise their appetite has decreased significantly as the decline is slow and progressive. Protein and fibre are often poorly consumed in the diets of older adults with decreased appetite, but essential for health and well-being. Interventions designed to increase appetite, or increase dietary intake despite a reduced appetite, should therefore be key to preventing undernutrition (i.e. protein-energy malnutrition as well as nutrient deficiencies). However, treatment strategies for poor appetite are not well-established.

In this multi-centre randomised controlled trial conducted in Ireland, Germany, and Italy, a two-by-two factorial design will define the individual and combined impact of two intervention conditions over 12 weeks: 1) personalised diet with focus on plant-based protein plus fibre; and 2) physical activity.

At each centre, 60 older adults (180 in total) will be randomly allocated to one of the following four groups over a 12 week period: 1) personalised diet plus physical activity program (PD + PA), 2) usual diet plus physical activity (PA), 3) personalised diet and no PA (PD), and 4) control (usual diet, no PA).

Using identical procedures, two testing visits will be completed before and after the 12 intervention or control period.

Titolo ufficiale

Innovative PlAnt Protein Fibre and Physical Activity Solutions to Address Poor AppEtite and PrevenT UndernutrITion in OldEr Adults (APPETITE)

Condizioni
Perdita di appetitoInattività fisicaMalnutrizioneAnorexia of AgingInvecchiamentoInvecchiamento sano
Pubblicazioni
Articoli scientifici e documenti di ricerca pubblicati su questo studio clinico:
Altri ID dello studio
  • LS-21-96-Roche
  • JPI-ERA-HDHL PREVNUT-2020-1 (Altro numero di finanziamento) (Health Research Board (HRB))
Numero NCT
NCT05608707
Data di inizio (effettiva)
2022-09-22
Ultimo aggiornamento pubblicato
2024-12-09
Data di completamento (stimata)
2025-09
Arruolamento (previsto)
180
Tipo di studio
Interventistico
FASE
N.D.
Stato
Attivo, non in arruolamento
Parole chiave
appetite
energy intake
nutrition
older adults
Physical activty
Scopo principale
Prevenzione
Allocazione
Randomizzato
Modello di intervento
Fattoriale
Mascheramento
Nessuno (studio in aperto)
Bracci / Interventi
Gruppo/Braccio di partecipantiIntervento/Trattamento
SperimentalePersonalised diet plus physical activity intervention
A personalised diet intervention involving the incorporation of the developed plant-based protein and fibre product. Participants will also undertake 2 weekly group exercise sessions incorporating strength and balance exercises, along with home-based exercise
Intervento di attività fisica
The 12 week intervention will involve 2 weekly group exercise sessions incorporating strength and balance exercises, along with home-based exercise focused on increasing time spent walking.
Personalised Nutrition Intervention
Two Plant-based Protein and Fibre (PPF) product products have been selected from six initially developed, with best amino acid blend, taste, and bioavailability. Participants will be provided with the PPFs to consume daily as part of a personalised diet over 12 weeks.
SperimentaleUsual diet plus physical activity
Participants will consume their usual diet and undertake 2 weekly group exercise sessions incorporating strength and balance exercises, along with home-based exercise
Intervento di attività fisica
The 12 week intervention will involve 2 weekly group exercise sessions incorporating strength and balance exercises, along with home-based exercise focused on increasing time spent walking.
SperimentalePersonalised diet plus usual physical activity
A personalised diet intervention involving the incorporation of the developed plant-based protein and fibre product.
Personalised Nutrition Intervention
Two Plant-based Protein and Fibre (PPF) product products have been selected from six initially developed, with best amino acid blend, taste, and bioavailability. Participants will be provided with the PPFs to consume daily as part of a personalised diet over 12 weeks.
Nessun interventoControl (usual diet and physical activity)
This arm will not be given any nutritional or physical activity support. They will be instructed to carry on with their usual activities.
N.D.
Esito primario
Misure di esitoDescrizione della misuraArco temporale
Ad libitum energy intake (kcal)
12-week change in energy intake assessed at an an ad libitum lunch test meal
To be assessed at baseline and following a 12-week intervention or control period
Changes in subjective appetite sensations
12-week change in appetite to be assessed by Visual Analogue Scale (VAS) during a test meal challenge. The VAS is a validated tool for assessing subjective sensations such as hunger, fullness and desire to eat. On each 100-mm line, an appetite (hunger, fullness, desire to eat) sensation was paired with the opposing sensation (for example, 'hungry' and 'not hungry').
To be assessed at baseline and following a 12-week intervention or control period
Esito secondario
Misure di esitoDescrizione della misuraArco temporale
7-day physical activity score as assessed by ActivPAL v4.0
12-week change in physical activity score will be assessed using 7-day accelerometery data. This is a validated device that is installed onto an individuals thigh for continuous readings. The data generated describes the amount of time spent engaging in physical activities and sedentary activities, and gives an output score in MET.h (Metabolic EquivalenT hour). This is a measure of energy usage over and above what is required at rest, where 1MET is equivalent to oxygen uptake of 3.5ml/kg body weight/minute
To be assessed at baseline, prior to commencing the intervention, and during week 12 of the intervention or control period
Resting Energy Expenditure (REE) (sub-sample)
12-week change in resting energy expenditure will be assessed using indirect calorimetry
To be assessed at baseline and following a 12-week intervention or control period
Handgrip strength
12-week change in handgrip strength will be assessed using a Jamar hydraulic hand dynamometer
To be assessed at baseline and following a 12-week intervention or control period
Isometric knee extension strength
12-week changes in isometric leg strength will be assessed using a seated leg extension dynamometer
To be assessed at baseline and following a 12-week intervention or control period
Cardiorespiratory fitness
12-week change in cardiorespiratory fitness will be assessed using the 400-meter walk test
To be assessed at baseline and following a 12-week intervention or control period
Physical performance
12-week change in physical function will be assessed using the Short Physical Activity Battery (SPPB)
To be assessed at baseline and following a 12-week intervention or control period
Participants subjective rating of perceived Quality of Life as assessed by the EQ-5D-5L
12-week changes in perceived quality of life will be assessed using the EuroQol (European Quality Of Life) questionnaire (EQ-5D-5L). This consists of self-assessed rating of health under 5 dimensions (Mobility, Self-Care, Usual Activity, Pain/Discomfort, Anxiety/Depression), and perceived overall health on a magnitude scale (0-100) anchored with opposing statements (0= the worst health you can imagine; 100= the best health you can imagine).
To be assessed at baseline and following a 12-week intervention or control period
Body composition (fat mass, fat free mass) by air displacement phlethysmography (sub-sample)
12-week change in body composition will be assessed using air displacement plethysmography (Bodpod).
To be assessed at baseline and following a 12-week intervention or control period
Cognitive Dietary Restraint
12-week change in dietary restraint will be assessed using the Cognitive Dietary Restraint (CDR) subscale of the Three Factor Eating Questionnaire (TFEQ). The questionnaire consists of a subscale of 6 questions relating to cognitive dietary restraint from the orignal 50 item questionnaire. The questions are a mix of 'true/false', and likert scale type answers.
To be assessed at baseline and following a 12-week intervention or control period
Dietary Record (energy, protein and fibre intake)
12-week change in energy, protein and fibre intake assessed using a three-day non-weighed dietary record
To be assessed at baseline and following a 12-week intervention or control period
Appetite hormones (Ghrelin, GLP-1, & PYY) (sub-sample)
12-week change in appetite-related gut hormone response to a fixed meal. Assessed in circulating peripheral bloods at fasting, and at regular intervals postprandially (minute 30, 60, 90, 120, 150, \& 180).
To be assessed at baseline and following a 12-week intervention or control period
Gut metabolomic profiles and gut microbiome diversity
12-week change in gut microbiota quality and diversity assessed by faecal matter and faecal water.
To be assessed at baseline and following a 12-week intervention or control period
Blood hormone and metabolite profile
12-week change in fasting peripheral blood profile (insulin, leptin, glucose, amino acid, fatty acid)
To be assessed at baseline and following a 12-week intervention or control period
Body composition by Bioelectrical Impedance Analysis (BIA)
Body composition will be assessed by BIA across all sites at baseline and post intervention. BIA is a quick non-invasive method of measuring body composition. Bioelectrical impedance analysis (BIA) measures body composition based on the rate at which an electrical current travels through the body. Body fat (adipose tissue) causes greater resistance (impedance) than lean mass and slows the rate at which the current travels. The device provides an output of absolute (Kg) and percentage (% of total mass) of fat mass (FM) and fat-free mass (FFM).
To be assessed at baseline and following a 12-week intervention or control period
Appetite by Simplified Nutritional Appetite Questionnaire (SNAQ)
The SNAQ questionnaire is used to assess an older adults usual appetite. The SNAQ is a self-administered questionnaires adapted from the Appetite, Hunger and Sensory Perception questionnaire (AHSP), an appetite assessment tool validated among community-dwelling older adults. It consists of 4 multiple choice statements, where an individual reads the beginning of the statement and is presented with 5 options that best describe their situation. Each question derives a score between 1 - 5 with lower scores indicating poorer appetite. The questionnaire scores between 4 - 20 with scores \</= 14 indicating poor appetite.
To be assessed at baseline and following a 12-week intervention or control period
Test meal palatability by Visual Analogue Scale (VAS)
Rating of the breakfast and lunch test meals by visual analogue scales (VAS). The VAS is a validated tool for assessing subjective sensory experience. On each 100-mm line, a question is asked relating to sensory aspects of the meal (E.g., How pleasant was the meal?). The subject will mark along the 100mm line where they feel their experience, in terms of the question, rests. On ether end of the 100mm line are opposing terms (E.g., "not at all", "extremely").
To be assessed at baseline and following a 12-week intervention or control period
Body weight (kg)
Body weight will be measure using a calibrated scales, shoes and heavy clothing removes, and recorded in kilograms.
To be assessed at baseline and following a 12-week intervention or control period
Standing height (cm)
Height will be measured in centimetres using a stadiometer. Participants will be measured barefoot and asked to take a full inhalation prior to stepping out from the device. Measurements are taken at the peak of the inhalation.
To be assessed at baseline and following a 12-week intervention or control period
Calf circumference (cm)
Calf circumference is measures using a non-stretch tape measure at the widest part of the calf muscle and recorded in centimetres.
To be assessed at baseline and following a 12-week intervention or control period
Perception and evaluation of the trial
Questionnaire specific to the project. This questionnaire will serve to provide feedback about participants experience while enrolled on the project. The questionnaire will include a series of Likert style questions and open-ended questions. The purpose is the provide feedback to the study team on what participants liked or disliked about the experience. This will serve to inform future management of studies.
End of trial (up to 18-weeks)
Body composition by Dual-energy X-ray absorptiometry (DXA) (sub-sample)
DXA will be performed on a sub-sample of participants enrolled on the APPETITE study. A DXA can involves a large scanning arm being passed over the body to measure compartments of the body structure. As the scanning arm is moved slowly over your body, a narrow beam of low-dose X-rays will be passed through the part of your body being examined. DXA is a quick and non-invasive scan that provides in-depth analysis of the main components of your body; fat, muscle and bone.
To be assessed at baseline and following a 12-week intervention or control period
Motor Unit Signalling (sub-sample)
by electromyography (EMG)
To be assessed at baseline and following a 12-week intervention or control period
Motor Unit Number
from muscle biopsy
To be assessed at baseline and following a 12-week intervention or control period
muscle signalling related to muscle plasticity, metabolism, denervation and muscle capillarization (sub-sample)
This refers to the analyses of muscle biopsies. Biopsies will be taken using MEDAX/BF14100-C0; Bio-Feather with coaxial 14 g 10 cm. The following parameters will then be measured in the sample using western blot with specific antibodies for total proteins or by their activated phosphorylated form: 1) markers of denervation (AChR ; agrin/MuSK/Lrp4, NCAM, Myog); 2) markers of protein turnover (atrogin1, MURF1, LC3, BNIP3, Akt-dependent mTOR and FoxO); 3) markers of mitochondrial dynamics (OPA1, DRP1) and; 4) markers of energy metabolism pathways (AMPK and PGC1alpha).
To be assessed at baseline and following a 12-week intervention or control period
Innate immune training of macrophages
Trained immunity describes the long-term functional reprogramming of innate immune cells after exposure to a primary insult which leads to an augmented response upon stimulation with the same ligand after returning to a non-activated state. Will habitual ingestion of plant protein combined with PA results in increased ability of macrophages to undertake innate immune train in adults over the age of 65. Effects will be quantified by comparing the presence of TNF alpha in human monocytes at baseline and following a 12-week intervention.
To be assessed at baseline and following a 12-week intervention or control period
Criteri di eleggibilità

Età idonea
Adulto anziano
Età minima
65 Years
Sessi idonei
Tutti
Accetta volontari sani
Sì
  • Community-dwelling,
  • Age 65+ years,
  • BMI 19.5-30.4kg/m2,
  • Inactive (<150 minutes of moderate to vigorous physical activity per week and no regular resistance training),
  • Have proof of Covid-19 vaccination

  • Major cognitive impairment (MMSE ≤24),
  • Uncontrolled Clinical depression (CES-D >16),
  • Medical condition or current medication known to impact appetite or energy intake,
  • Other medical condition that may impact ability to participate in study or study outcomes,
  • Heavy smoker (>10/day),
  • Plans to relocate out of the study area within the next 6 months,
  • Inability to come to study centre/PA program location,
  • Currently participating in another intervention study,
  • Inability to participate in physical activity,
  • Unable to walk across a room,
  • Allergic to or unwilling to consume any of the study test foods,
  • Loss of taste or smell associated with COVID-19,
  • Unwilling to be randomised to any intervention group.
University College Dublin logoUniversity College Dublin
  • 🏛️Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement
  • 🎓Friedrich-Alexander-Universität Erlangen-Nürnberg
  • 🎓University of Padova
Nessun dato di contatto
3 Centri dello studio in 3 paesi
UNIPD, Padua, Italy
FAU, Nuremberg, Germany

Leinster

School of Public Health, Physiotherapy and Sports Science, Dublin, Leinster, Ireland