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The Effects of Texture Modified Diets on Dietary Intake and Appetite Responses in Older Adults

Investigating the Influence of Texture Modified and Protein-enriched Meals on Dietary Intake and Appetite Responses in Healthy Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04521374
Enrollment
21
Registered
2020-08-20
Start date
2020-09-07
Completion date
2022-09-06
Last updated
2022-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Older Adults

Keywords

Older adults, Texture modified diet, Protein fortification, Appetite, Dietary intake, Food first

Brief summary

This study aims to investigate the effects of equicaloric texture modified and regular meals that are either fortified with protein or not on dietary intake and satiety in older adults (65+) living in the United Kingdom (UK).

Detailed description

* To investigate whether there are any differences in appetite responses following a texture modified meal compared to a standard meal. * To investigate whether protein-enriched versions of a texture modified meal and/or standard meal affects satiety and subsequent intake in healthy older adults. * To investigate the effects of a texture modified diet, standard diet and their protein-enriched versions on gastric emptying in healthy older adults.

Interventions

BEHAVIORALPreload meals that are solid or texture modified and are fortified with protein or not fortified with protein

Immediately after consuming the preload meal, volunteers will use a 100mm visual analogue scale (VAS) to rate their liking towards the meal, their hunger, fullness, desire to eat and prospective food intake. Subsequently, they will record these every 30 minutes until they consume their ad-libitum dinner

Sponsors

University of Reading
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Masking description

All samples provided to the participant are labelled with 3 digit random codes

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* aged 65 years or over (no upper age limit); * be within body mass index range (18.5-34.9kg/m2 ); * regularly consume 3 meals a day (breakfast by 11am, lunch and dinner); * be able to accept test meals provided; * be able to feed themselves; * be able to give informed consent; i.e not lacking mental capacity; * Have access to a kitchen, freezer and fridge. * Have access to a telephone. * understand English.

Exclusion criteria

* Diagnosed with coronavirus (COVID-19) or have had it in the last 4 weeks. * have any existing neurological or gastrointestinal condition; * have Cancer; * have no current chewing or swallowing difficulties (such as dysphagia); * have no existing cognitive or psychiatric disorder; * taking medications that can significantly affect taste changes, appetite or gastric emptying; * be on a special or therapeutic diet; * have any food allergies or intolerances that will be worsened with meals provided in the study; * have a history of drug or alcohol misuse; * smoke more than 10 cigarettes a day.

Design outcomes

Primary

MeasureTime frameDescription
Intake at ad-libitum dinner4 days in total (one measurement per study day)Intake at the ad-libitum meal is measured (grams). Volunteers are instructed to eat only until they feel comfortable satisfied and are given 20 min to consume the meal.

Secondary

MeasureTime frameDescription
Ratings (Appetite, hedonic and palatability) of breakfast, preload lunch and ad-libitum dinnerRegular ratings each study visit, 4 days in totalAppetite, hedonic and palatability ratings are assessed using validated 100 mm Visual Analogue Scales (VAS, sscale 0-100). Before and immediately after breakfast and assessed every 30 min for 360 min
Gastric emptyingRegular samples each study visit, 4 days in totalGastric emptying will be measured using 13C-labelled sodium acetate which will be added into a bottle of water. This will be consumed alongside preload meal. Measurements will be taken every 1 hour after consumption of breakfast up to preload, then every 15 min after the preload for 180 min.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026