Let's Increase Fuerza (Strength) Through Exercise and Diet
NCT06884501, Not applicable, Not yet recruiting, University of Illinois at Urbana-Champaign
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Let's Increase Fuerza (Strength) Through Exercise and Diet | ClinicalTrials.gov |
| NCT number | NCT06884501 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 90 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | University of Illinois at Urbana-Champaign | ClinicalTrials.gov |
| Conditions | Older Adults (50-90 Years), Cognition, Physical Activity | ClinicalTrials.gov |
| Interventions | Latin dance, MIND diet, and Strength training, Latin dance and MIND Diet | ClinicalTrials.gov |
| First posted | 2025-03-19 | ClinicalTrials.gov |
| Last updated | 2025-07-04 | ClinicalTrials.gov |
Registered outcomes 19
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Stroop Neuropsychological Screening Test (Trennerry et al., 1989) | Change in score from baseline to 6 months | Stroop Test will be used to assess executive function. In Stroop C, participants are shown a list of colors printed in conflicting color ink and are asked to read words (names of colors). The second part of this task is Stroop CW in which participants are shown a list of colors printed in conflicting color ink and are asked to say the color of the ink the word is printed. The scores are the number of words named correctly in 30 seconds and the number of colors named correctly in 30 seconds subtracting the number of errors. respectively. | ClinicalTrials.gov |
| Primary | Word fluency Test (Welsh et al., 1994) | Change in score from baseline to 6 months | Word Fluency will be used to assess executive function. The Word Fluency Test asks participants to name as many animals (part 1) or fruits and vegetables (part 2) as possible in 60 seconds. The score is the sum of the number of animals and the number of fruits and vegetables named. | ClinicalTrials.gov |
| Primary | Digit Span Test (Wechsler, 1987) | Change in score from baseline to 6 months | Digit Span Test will be used to measure executive function. Digit Span Forward \& Backward will be used to assess working memory. Digit strings of increasing length will be read, and the participant is asked to repeat each string forward (Digit Span Forward) or backward (Digit Span Backward). The score is the number of correctly retrieved strings in each part | ClinicalTrials.gov |
| Primary | Trail Making Test (A&B) | Change in scores from baseline to post-intervention 6 months | Trail Making Test (A\&B) will be used to measure executive function. Part A consists of numbers spread out in a grid with a dedicated start and end point. Participants must trace in sequential order. Part B will consist of numbers and letters in sequential order spread across a grid with a start and end point as well. Participants much trace the starting number to letter. Scoring will be based on seconds needed to complete each test with Part A having a max of 100 seconds and Part B with a max of 300 seconds. Test will discontinue when the time limit has been reached. | ClinicalTrials.gov |
| Secondary | Minutes per day of light and moderate-to-vigorous physical activity via GT3x Actigraph Accelerometer | Change in minutes per day of light and moderate-to-vigorous physical activity from baseline to post-intervention 6 months | Device-assessed physical activity via GT3x Actigraph accelerometers will be used to assess minutes per day spent in light physical activity and moderate-to-vigorous physical activity. | ClinicalTrials.gov |
| Secondary | Godin-Shephard Leisure-Time Physical Activity Questionnaire | Change in score from baseline to 6 months | The Godin-Shephard Leisure-Time Physical Activity Questionniare is 2-item questionnared used to assess leisure time physical activity. | ClinicalTrials.gov |
| Secondary | Non-exercise Cardiorespiratory Fitness Questionnare | Change in score from baseline to 6 months | The non-exercise cardiorespiratory fitness questionnaire estimates cardiorespiratory fitness using age, sex, BMI, resting heart rate, and self-reported physical activity. | ClinicalTrials.gov |
| Secondary | Spectroscopy-Based Veggie Meter® | Change in scores from baseline to post-intervention 6 months | The Veggie Meter (VM; Longevity Link Inc., Salt Lake City, UT, USA) is a commercially available device that uses reflection spectroscopy to measure the level of carotenoid pigments in a person's skin by scanning the tip of the finger. Scores range from 0-800. | ClinicalTrials.gov |
| Secondary | Plasma Structural Lipidomics | Change in scores from baseline to post-intervention 6 months | A lipidomics profile will be assessed from the plasma provided. This will be analyzed with Liquid Chromatography coupled to Mass Spectrometry to identify over 800 lipid species | ClinicalTrials.gov |
| Secondary | National Institutes of Health (NIH) Toolbox: Perceived Stress Fixed Form Age 18+ v2.0 | Change in scores from baseline to post-intervention 6 months | NIH Tool box measure of perceived stress is a self-reported measure that assesses how unpredictable, uncontrollable, and overloaded respondents find their lives. 10 items are administered using a 5-point scale, with options ranging from "never" to "very often". Higher scores are indicative of higher perceived stress. | ClinicalTrials.gov |
| Secondary | National Institutes of Health (NIH) Toolbox General Life Satisfaction Fixed Form A Age 18+ v2.0 | Change in scores from baseline to post-intervention 6 months | NIH Tool box measure of general life satisfaction assesses global feelings and attitudes about one's life. 5 items are administered using a 5 and 7-point scale, ranging from "strongly disagree" to "strongly agree". Higher scores are indicative of higher general life satisfaction. | ClinicalTrials.gov |
| Secondary | National Institutes of Health (NIH) Tool Box: Sadness Fixed Form Age 18+ v2.0 | Change in scores from baseline to post-intervention 6 months | NIH Toolbox measure of depression/sadness assesses negative mood, negative views of self, and negative social cognition. 8 items are administered using a 5-point scale ranging from "never" to "always". Higher scores are indicative of more sadness. | ClinicalTrials.gov |
| Secondary | National Institues of Health (NIH) Toolbox Loneliness Fixed Form Age 18+ v2.0 | Change in scores from baseline to post-intervention 6 months | NIH Toolbox measure of loneliness assesses perceptions of loneliness using 5 items, responses from a 5-point scale ranging from "never" to "always". Higher scores are indicative of more loneliness. | ClinicalTrials.gov |
| Secondary | MIND Diet Adherence | Change in scores from baseline to post-intervention 6 months | Block 2005 Food Frequency Questionnaire will be used to compute MIND diet scores. Frequency of consumption for food items was assigned a score of 0, 0.5, or 1, where scores ranged from 0 (lowest adherence) to 15 (highest adherence) | ClinicalTrials.gov |
| Secondary | Blood pressure | Change from baseline to post-intervention 6 months | Blood pressure will be assessed using Omron blood pressure monitors | ClinicalTrials.gov |
| Secondary | Fasting Blood glucose | Change from baseline to post-intervention 6 months | 2, 3 mL blood samples will be obtained to assess fasting blood glucose. | ClinicalTrials.gov |
| Secondary | Waist Circumference | Change from baseline to post-intervention 6 months | Waist circumference will be measured using a tape measure reported as CM. | ClinicalTrials.gov |
| Secondary | DEXA | Change from baseline to post-intervention 6 months | A DEXA scan is a type of x-ray that will be used used to measure body composition. | ClinicalTrials.gov |
| Secondary | MOCA-Blind Version 8.1 | Change in score from baseline to 6 months | The MOCA-Blind assesses attention, concentration, memory, language, conceptual thinking, calculations, and orientation. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 4
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Digit Span Test | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
| Trail Making Test A | Primary outcome | ConductCognition |
| Trail Making Test B | Primary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)