Can a tailored diet boost brain and body health in denture-wearers?
NCT ID NCT07692828
First seen Jul 09, 2026 · Last updated Jul 10, 2026 · Updated 1 time
Summary
This study tests a 6-month nutritional program for adults aged 60–80 who wear complete dentures. Participants receive personalized dietary advice, meal plans, cooking workshops, and a mobile app. The goal is to see if the program improves diet quality, chewing ability, muscle strength, cognitive performance, and quality of life compared to usual eating habits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Nutritional intervention (dietary counseling, meal plans, cooking workshops, mobile app)
- What this could lead to
- If effective, this dietary program could help older denture-wearers eat better, maintain muscle strength, and stay mentally sharp.
- What could go wrong
- This is a small early-stage study with only 40 participants, so results may not apply broadly. The intervention requires significant commitment and may not work for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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May 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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60 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Men and women aged 60 to 80 years. * Systemically healthy individuals or those with controlled chronic systemic conditions under regular medical supervision. * Functionally independent individuals, or those with a dedicated family member or caregiver available to provide support throughout the study period. * Wearers of both maxillary and mandibular complete removable dentures. * Adequate stability, retention, and functionality of both complete dentures allowing the participant to chew effectively during daily meals (accepting minor retention or stability limitations in the mandibular prosthesis, provided routine functional mastication is maintained). * Acceptable centric occlusion and jaw relationship allowing functional mastication. * Intact oral mucosa without active lesions or severe soreness in the denture-bearing areas. Exclusion Criteria: * Altered salivary flow (hyposalivation or xerostomia) identified via anamnesis and sialometry, with an unstimulated salivary flow rate \< 0.1 mL/min or a stimulated salivary flow rate \< 0.5 mL/min. * Active oral mucosa diseases or lesions (e.g., cheilitis, denture stomatitis, ulcers, or aphthae) verified through intraoral examination. * Diagnosis of a major neurocognitive disorder by a qualified professional, verified via medical records and/or caregiver interview. * Color blindness (daltonism or color vision deficiency). * Presence of signs or symptoms of temporomandibular disorders (TMD). * Known history of allergy to peanuts or latex. * Underweight or severe undernutrition, defined as a Body Mass Index (BMI) \< 18.5 kg/m².
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Universidad de La Frontera
Temuco, Cautín, 4780000, Chile
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Other studies related to the condition(s) this trial covers.
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