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Trial · NCT05689554

Reducing CNS-Active Medications to Prevent Falls and Injuries in Older Adults

NCT05689554, Not applicable, Completed, University of Washington; results first posted 2024-12-09

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Reducing CNS-Active Medications to Prevent Falls and Injuries in Older Adults. Trials, record NCT05689554. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05689554

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Trial

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

Title
Reducing CNS-Active Medications to Prevent Falls and Injuries in Older Adults
NCT number
NCT05689554
Status
Completed
Phases
Not applicable
Enrollment
2,367 participants, actual
Lead sponsor
University of Washington
Conditions
Aging, Accidental Fall
Interventions
STOP Falls Educational Intervention
First posted
2023-01-19
Last updated
2024-12-09
Results first posted
2024-12-09

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryMedically Treated Fallsup to 26 months following interventionFalls for which medical attention is sought
SecondaryMedication Discontinuation6 months following interventionTarget medication has not been prescribed for 90 days 6 months post intervention

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMedically Treated Fallsup to 26 months following interventionParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYMedication Discontinuation6 months following interventionNumber of participants who were not prescribed the target medication of interest 90 days post interventionParticipantsCOUNT_OF_PARTICIPANTS

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Medically Treated FallsIntervention328Participants
Medically Treated FallsUsual Care349Participants
Medication DiscontinuationInterventionOpioids32Participants
Medication DiscontinuationUsual CareOpioids40Participants
Medication DiscontinuationInterventionBenzodiazepines55Participants
Medication DiscontinuationUsual CareBenzodiazepines49Participants
Medication DiscontinuationInterventionTricyclic Antidepressants34Participants
Medication DiscontinuationUsual CareTricyclic Antidepressants23Participants
Medication DiscontinuationInterventionMuscle Relaxants34Participants
Medication DiscontinuationUsual CareMuscle Relaxants40Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDIntervention1,1069
Overall StudySTARTEDUsual Care1,2619
Overall StudyCOMPLETEDIntervention1,1069
Overall StudyCOMPLETEDUsual Care1,2619
Overall StudyNOT COMPLETEDIntervention00
Overall StudyNOT COMPLETEDUsual Care00

Adverse events2

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

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousSerious adverse drug withdrawal events involving opioids or sedative-hypnoticsGeneral disordersIntervention101,10610
seriousSerious adverse drug withdrawal events involving opioids or sedative-hypnoticsGeneral disordersUsual Care41,2614

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityIntervention861,106
Total, all-cause mortalityUsual Care721,261
Total, other adverse eventsIntervention01,106
Total, other adverse eventsUsual Care01,261
Total, serious adverse eventsIntervention101,106
Total, serious adverse eventsUsual Care41,261

Papers3

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
37170329DERIVEDPubMed
39052289DERIVEDPubMed
39360568DERIVEDPubMed

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 comparisons3

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

ComparisonSource
Intervention vs Usual Care: Medically Treated FallsTrial comparisons
Intervention vs Usual Care: deaths from any causeTrial comparisons
Intervention vs Usual Care: serious adverse eventsTrial comparisons

Tests0

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

None in this release.

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/NCT05689554

GET https://conductscience.org/api/trials/v1/NCT05689554/registered