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Trial · NCT07692828

Nutritional Intervention for Older Adults With Complete Dentures

NCT07692828, Not applicable, Recruiting, Universidad de La Frontera

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Nutritional Intervention for Older Adults With Complete Dentures. Trials, record NCT07692828. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07692828

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Nutritional Intervention for Older Adults With Complete Dentures
NCT number
NCT07692828
Status
Recruiting
Phases
Not applicable
Enrollment
40 participants, estimated
Lead sponsor
Universidad de La Frontera
Conditions
Edentulism Complete, Denture, Complete, Mastication Disorder
Interventions
Nutritional Intervention
First posted
2026-07-09
Last updated
2026-09-17

Source ClinicalTrials.gov

Registered outcomes23

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMasticatory PerformanceT0 (month 0), T1 (month 3) and T2 (month 6).
Measurement of food fractionation capacity. Participants will chew a standardized food (peanuts) for 20 cycles; the particles will be dried and processed through a sieving system (sieves from 4.0 mm to 870 μm) to determine the percentage of fractionation.
PrimaryDiet Quality AssessmentT0 (month 0), T1 (month 3) and T2 (month 6).
Diet quality will be assessed using the Chilean Healthy Eating Index (Índice de Dieta Mediterránea for Chile, IDM-Chile), which allows the evaluation of adherence to healthy dietary patterns in the study population.
PrimaryPerceptions of Edentulism and Adaptation to Complete Removable DenturesBetween month 0 and month 1 (collected during the initial phase of the study to capture prior experiences and avoid intervention bias).
A qualitative assessment using a Grounded Theory framework conducted through semi-structured individual interviews to explore older adults' perceptions regarding their experiences with tooth loss, rehabilitation with complete removable dental prostheses, and their natural functional and social adaptation strategies in daily life. Interviews (30-60 minutes) will be audio-recorded, transcribed verbatim, and analyzed concurrently using ATLAS.ti software through progressive coding (open, axial, and selective) to develop a substantive explanatory model.
SecondaryMasticatory Kinematics: Number of Chewing CyclesT0 (month 0), T1 (month 3) and T2 (month 6).The total number of chewing cycles recorded during the mastication of a standardized food (peanuts), quantified using a 3D electromagnetic articulograph (AG501).
SecondaryMasticatory Kinematics: Chewing Cycle AreaT0 (month 0), T1 (month 3) and T2 (month 6).Assessment of chewing cycles focusing on the area, measured in square millimeters (mm²) using a 3D electromagnetic articulograph (AG501).
SecondaryMasticatory Kinematics: Masticatory FrequencyT0 (month 0), T1 (month 3) and T2 (month 6).Assessment of the masticatory frequency during mastication, measured as the number of cycles per second (cycles/s) using a 3D electromagnetic articulograph (AG501).
SecondaryMasticatory Kinematics: Masticatory SpeedT0 (month 0), T1 (month 3) and T2 (month 6).Assessment of chewing focusing on the movement velocity, measured in millimeters per second (mm/s) using a 3D electromagnetic articulograph (AG501).
SecondaryMaximum Bite ForceT0 (month 0), T1 (month 3) and T2 (month 6).Measurement of maximum voluntary contraction in Newtons (N) using a digital gnathodynamometer placed between the first prosthetic molars.
SecondaryMasticatory Muscles ThicknessT0 (month 0) and T2 (month 6).Evaluation of the thickness of the masseter and anterior temporalis muscles, measured in millimeters (mm) using a portable ultrasound device with a linear transducer.
SecondarySalivary Biomarkers: CortisolT0 (month 0) and T2 (month 6).
Laboratory analysis of saliva samples to quantify cortisol concentration, a biomarker of physiological stress, samples will be analyzed using a Synergy HT Multimodal Reader (Biotek, USA). The outcome will be determined via enzyme-linked immunosorbent assay (ELISA) and expressed in nanograms per milliliter (ng/mL).

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers9

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
21684773BACKGROUNDPubMed
22024405BACKGROUNDPubMed
23282773BACKGROUNDPubMed
23659650BACKGROUNDPubMed
26639926BACKGROUNDPubMed
28393987BACKGROUNDPubMed
28830699BACKGROUNDPubMed
29075647BACKGROUNDPubMed
35042607BACKGROUNDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests1

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed as
Stroop Color-Word TestSecondary outcome

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07692828

GET https://conductscience.org/api/trials/v1/NCT07692828/registered?page=2