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Trial · NCT04118985

Compensatory Training to Support Brain Healthy Lifestyle Changes in Those at Risk for Alzheimer's Disease

NCT04118985, Not applicable, Completed, Mayo Clinic

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Compensatory Training to Support Brain Healthy Lifestyle Changes in Those at Risk for Alzheimer's Disease. Trials, record NCT04118985. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04118985

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Trial

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

Title
Compensatory Training to Support Brain Healthy Lifestyle Changes in Those at Risk for Alzheimer's Disease
NCT number
NCT04118985
Status
Completed
Phases
Not applicable
Enrollment
21 participants, actual
Lead sponsor
Mayo Clinic
Conditions
Cognitive Symptom, Pre Senile Dementia, Alzheimer Disease
Interventions
Cognitive rehabilitation and health behavior change intervention, Self-implementation
First posted
2019-10-08
Last updated
2020-11-17

Source ClinicalTrials.gov

Registered outcomes14

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

ListOutcomeTime frameDescription
PrimaryEveryday Compensation Questionnairebaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsself-report and informant report if an informant is available of compensatory strategy use; range 0-148 with higher scores indicating more compensatory use
PrimaryLifestyle Activities Questionnairebaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsself-report of cognitive activities, range 13-65 with higher scores indicating more activity
PrimaryBrainHQbaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsNumber of minutes on BrainHQ computer exercise program
PrimaryPhysical Activities Questionnairebaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsself-report of physical activity; scores include number of days per week across 7 activity types and number of minutes in each activity when completed.
PrimaryMindful Attention Awareness Scalebaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsself-report of mindfulness, range of 11-66 with higher scores indicating more mindful daily experience
SecondaryEveryday Cognitionbaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsself-report of everyday functioning, range 39-156 with higher scores indicating more problems in daily functioning
SecondaryQuality of Life (in aging and cognitive health)baseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsself-report of quality of life, range of 13-52 with higher scores indicating better quality of life
SecondaryPsychological well-beingbaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 months
self-report of psychological well-being/happiness; there is a total score plus subscales of autonomy, environmental mastery, personal growth, positive relations with others, purpose in life, self-acceptance. Each subscale has 9 items for a total of 54 items. Total scores range from 54-324 with higher scores indicating higher psychological well being. Each subscale ranges from 9-54 with higher scores indicating greater well-being on that construct.
SecondaryCenters for Epidemiological Studies - Depressionbaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsself-report of symptoms of depression.Range 0-60 with higher scores indicating more depression
SecondaryCognitive measure of memorybaseline, change from baseline at end of 10 week treatment, change from baseline at 3 months, change from baseline at 6 monthsHopkins Verbal Memory test. Staff administered standardized verbal memory task. Scores include total words recalled and total recalled after a delay with higher scores indicating greater recall

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.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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.

Tests3

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

TestNamed asSource
Stroop Color-Word TestSecondary outcomeConductCognition
Symbol CodingSecondary outcomeConductCognition
Verbal FluencySecondary outcomeConductCognition

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license 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/NCT04118985

GET https://conductscience.org/api/trials/v1/NCT04118985/registered