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NCT Number: NCT07636369

The SAVOR Study: Appetite and Physiological Responses

The study aims to identify key physiological factors that differentiate older adults with healthy appetites from those experiencing appetite decline. The investigators hypothesize that seniors experiencing appetite decline will exhibit distinct oro-sensory, gastrointestinal, and hormonal profiles compared to seniors with healthy appetites, suggesting underlying biological mechanisms contributing to reduced appetite.

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Key information

Age range

65 year–74 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Appetite decline in older adults, or anorexia of aging, is a prevalent geriatric syndrome associated with decreased quality of life, increased risk of malnutrition, and accelerated decline in health. While current nutritional guidelines often emphasize increasing nutrient density, these strategies often fail to address the root causes of diminished appetite. Emerging research highlights the critical role of age-related physiological changes, particularly dysregulation of the gut-brain axis, altered sensory perception, and hormonal imbalances, in suppressing appetite. Notably, existing evidence is largely derived from Western populations, which may not fully reflect the influence of cultural and lifestyle factors on appetite in Asian seniors. This leaves a significant gap in understanding and addressing appetite loss within this specific demographic. This study aims to address this gap by comprehensively investigating the physiological mechanisms underlying appetite regulation in Asian seniors, to identify key determinants that differentiate individuals with healthy appetites from those experiencing a decline. By assessing the relationships between oro-sensory function, gastric dynamics, neuro-hormonal regulation, gut microbiome composition and subjective appetite, this study seeks to provide a deeper understanding of the biological pathways driving appetite differences in this population. The findings of this study will lay the groundwork for future research aimed at developing culturally sensitive and effective interventions that can restore appetite, improve nutritional status, and ultimately enhance the health span and quality of life for older adults in Singapore and beyond. Furthermore, this work has the potential to drive innovation in the food and nutrition industry, leading to the development of tailored products and dietary strategies that effectively address the unique nutritional needs of aging populations, ultimately impacting public health recommendations and policies related to senior nutrition.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Postmenopausal female
  • Aged 65-74 years
  • Habitual breakfast consumer (consumes breakfast between 7am to 10am)
  • Willingness to consume meals and follow intervention protocol
  • English speaking

Exclusion criteria

  • BMI ≥ 27.5
  • Diagnosed with medical condition that may influence appetite or microbiome (e.g. diabetes, thyroid disorders, gastrointestinal diseases)
  • Currently taking any medications or supplements that may influence appetite or the microbiome (e.g. probiotics, antibiotics, appetite stimulants/suppressants) one month prior to their first visit in consultation with study physician, PI and study team
  • Following a special diet for weight management (e.g. low-calorie, low carbohydrate)
  • History of bariatrics surgery
  • Intentional attempt to change body weight or composition
  • History of severe vasovagal syncope (blackouts or near faints) following blood draw
  • Drug abuse within last 5 years
  • Excessive alcoholic beverage consumption > 2 servings per day (1 serving defined as 360 mL beer, 150 mL wine or 45 mL distilled spirits)
  • Smoking (cigarette, e-cigarette, cigar, pipe, vape)
  • Engaging in habitual vigorous physical activity (as defined by physical activity questionnaire-PAQ)
  • Loose teeth or jaw pain
  • Not missing > 2 non-wisdom molars
  • Involvement in other clinical studies that may influence the outcome of the study
  • A study team member or their immediate family member

Treatment and study plan

Shredded Chicken Congee

Other

This is a mixed meal tolerance test intended to elicit gut hormone responses reflective of real-world dietary patterns.

Primary outcomes

  1. Ad Libitum Lunch

    Time frame: Participants will be given 30 minutes to consume the meal until they are comfortably full, 180 minutes after the start of the intervention.

    Participants will be asked to eat as much of the stir-fried beehoon as they want until they are comfortably full, to measure the exact calorie intake by weighing the food before and after eating.

Secondary outcomes

  1. Palatability questionnaire

    Time frame: Administered after consuming test meal and after consuming the ad libitum meal.

    Palatability appetite questionnaire, rated on a visual analogue scale is a psychometric assessment tool where participants rate their subjective sensory experience-such as taste, smell, or pleasantness-by marking a point along a continuous 100 mm line anchored by opposing extremes (e.g., "extremely unpleasant" to "extremely pleasant").

  2. Appetite hormones

    Time frame: Blood samples will be collected at timepoints (t = -15 minute (baseline), 30, 60, 90, 120 and 180 minutes)

    GLP-1, PYY and Acyl-ghrelin will be used to measure hormones related to appetite.

  3. Subjective Appetite Questionnaire

    Time frame: Measurement is taken at t = -15 minute (baseline), 10, 30, 60, 90, 120 and 180 minutes

    A subjective appetite questionnaire utilizes a Visual Analogue Scale to quantify a person's current metabolic state by measuring four key sensations: hunger, fullness, desire to eat, and prospective food consumption.

  4. Gastric Ultrasound

    Time frame: Measurements will be taken at t = -15 minute (baseline), 15, 45, 105 and 165 minutes

    Gastric ultrasound will measure the gastric emptying rate postprandially.

  5. Stool collected using the OMNIgene and OMNImet

    Time frame: Baseline stool sample will be collected once between screening and intervention day.

    Stool sample will be collected in the OMNIgene-GUT and OMNImet-GUT tube for measurements that may include microbiome profiling, untargeted and targeted metabolome (e.g. bile acids and short-chain fatty acids profiling).

  6. Olfactory Acuity (SCENTinel)

    Time frame: Baseline measurement administered once during screening, takes approximately 5-10 minutes

    Olfactory acuity will be assessed using a simple, non-invasive SCENTinel rapid smell test. Participants will be presented with test cards containing various odors, and will be asked to detect, rate, and identify the odors. The test assesses the participant's ability to perceive and recognize smells, providing information on their overall sense of smell.

  7. Taste Acuity Test (WETT)

    Time frame: Baseline measurement administered once during screening, takes approximately 10-15 minutes

    The Waterless Empirical Taste Test (WETT) is a sensory method for assessing how well participants can recognise and detect basic tastes. Participants will taste pre-moistened, paper-based test strips for the five basic tastes: sweet, sour, salty, bitter, and umami.

  8. Blood plasma (Cytokines)

    Time frame: t = -15 minute (baseline), 30, 60, 90, 120, 180 minutes

    Blood samples may also be analyzed for indicators of inflammation including cytokines testing

  9. Blood plasma (Bile acids and short-chain fatty acids profiling)

    Time frame: t= -15 minute (baseline), 30, 60, 90, 120, 180 minutes

    Blood samples collected may be used to analyse biomarkers related to nutrition and digestive health e.g. bile acid and short-chain fatty acids profiling

  10. Bite Strength

    Time frame: Baseline measurement that may be administered once during screening or test session, as schedule and equipment permits. Takes only a few minutes.

    Bite strength will be measured using a bite force device (non-invasive) that records the maximum force a participant can exert while biting. Multiple measurements will be taken with rest periods in between to prevent fatigue.

  11. Tongue Strength (Tongue Pressure)

    Time frame: Baseline measurement that may be administered once during screening or test session, as schedule and equipment permits. Takes approximately 5 minutes.

    Tongue pressure will be measured using a device equipped with a disposable air-filled bulb placed between the tongue and the hard palate. Participants will be instructed to press the bulb with their tongue as firmly as possible for a few seconds. Multiple measurements will be taken with rest periods in between to ensure accuracy and prevent fatigue.

Other outcomes

  1. Health and Lifestyle questionnaire

    Time frame: Baseline measurement that is completed during screening visit

    This questionnaire is to evaluate the participant's eligibility for the study. It consist of participant information, medical and health history, lifestyle and diet, physical activity.

  2. 3-day food record

    Time frame: Administered between screening and actual test session, to be completed on 2 weekdays and 1 weekend.

    A 3-day food record is a detailed diary where participants document everything they eat and drink over two weekdays and one weekend day to provide an accurate snapshot of their typical nutritional intake. This is done using household measures (or digital scales), where exact portion sizes, cooking methods and brand names of all items are used.

  3. Gastrointestinal Symptom Rating Scale (GSRS)

    Time frame: Baseline measurement administered once during screening.

    The Gastrointestinal Symptom Rating Scale (GSRS) is a validated 15-item questionnaire used to assess the presence and severity of common digestive issues across five key areas: abdominal pain, reflux, diarrhea, constipation, and indigestion. Participants rate each symptom on a 7-point Likert scale-ranging from "no discomfort" to "very severe discomfort"-to provide a quantifiable measurement of their gastrointestinal well-being.

  4. Council on Nutrition Appetite Questionnaire (CNAQ)

    Time frame: Baseline measurement administered once during screening, takes approximately 5-10 minutes

    The Council on Nutrition Appetite Questionnaire (CNAQ) is a brief, 8-item screening tool designed to predict future weight loss by assessing a participant's appetite and dietary habits. It asks about sensations like hunger, how quickly a participant feel full, and how food tastes to determine if a participant is at risk for nutritional deficiencies or significant weight changes over the coming months.

  5. Pittsburgh Sleep Quality Index (PSQI)

    Time frame: Baseline measurement administered once during screening, takes approximately 5-10 minutes

    The Pittsburgh Sleep Quality Index (PSQI) is a validated 19-item questionnaire used to measure sleep quality and disturbances over a one-month timeframe. It evaluates seven key areas-including sleep duration, how long it takes to fall asleep, sleep disruptions, and daytime tiredness-to generate a single overall score that differentiates between "good" and "poor" sleepers in clinical research.

  6. Geriatric Depression Scale (GDS)

    Time frame: Administered once during screening, takes approximately 5 minutes

    The Geriatric Depression Scale (GDS) is a 30-item questionnaire-often shortened to a 15-item version-specifically designed to screen for depression in older adults. Unlike general depression scales, it uses a simple "yes" or "no" format and focuses primarily on psychological and mood-related symptoms rather than physical complaints (like aches or fatigue), which can often overlap with normal aging or other medical conditions.

  7. Dutch Eating Behavior Questionnaire (DEBQ)

    Time frame: Baseline measurement administered once during screening, takes approximately 10 minutes

    The Dutch Eating Behavior Questionnaire (DEBQ) is a 33-item psychometric scale used to assess the distinct psychological factors and eating styles that can lead to overeating or weight gain. It breaks eating behaviors down into three core subscales - emotional eating, external eating and restrained eating.

  8. Leeds Food Preference Questionnaire (LFPQ)

    Time frame: Baseline measurement administered once during screening, takes approximately 10-15 minutes

    The Leeds Food Preference Questionnaire (LFPQ) is a computer-based tool used in behavioral research to measure different psychological components of food preference and appetite. It uses a series of food images to evaluate two distinct aspects of food reward: explicit liking and implicit wanting. The tool categorizes these preferences across different food characteristics, specifically comparing high-fat vs. low-fat foods, and sweet vs. savory tastes.

  9. Three-Factor Eating Questionnaire (TFEQ)

    Time frame: Baseline measurement administered once during screening, takes approximately 10 minutes

    The Three-Factor Eating Questionnaire (TFEQ) is a validated psychometric tool used to measure three distinct dimensions of human eating behavior and cognitive dietary control. It evaluates eating habits across three primary subscales: cognitive restraint, disinhibition and hunger

  10. International Physical Activity Questionnaire (IPAQ)

    Time frame: Baseline measurement administered once during screening, takes approximately 10 minutes

    The International Physical Activity Questionnaire (IPAQ) is a validated tool that measures a person's physical activity levels over a 7-day period. It records the total time spent across four distinct intensities: vigorous activity (like running or heavy lifting), moderate activity (like steady cycling), walking, and weekday sitting time. These tracked minutes are converted into a standard metabolic score (MET-minutes/week), which is then used to classify an individual's overall physical activity level into one of three distinct categories: Low, Moderate, or High.

Study contacts

Contact information is provided by the study sponsor or research team.

Ashley Yu, BSc

CONTACT

[email protected]

Rina Quek, MSc

CONTACT

[email protected]

64074379

Sponsors and collaborators

Lead sponsor

Singapore Institute of Food and Biotechnology Innovation

Other Gov

Registry information

Official study title

Seniors' Appetite: Vibrant Opportunities for Revitalization (SAVOR)

Acronym: SAVOR

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 9, 2026
Registry last updated
Jun 9, 2026

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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