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Trial · NCT05266911

Registered outcomes17

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

ListOutcomeTime frameDescription
PrimaryFeasibility: Adherenceover 12 weeks (intervention duration)Percentage of exercise sessions completed (criteria: at least 70 precent)
PrimaryFeasibility: Recruitment4-6 month recruitment periodPercentage of eligible participants recruited (criteria: at least 65 precent)
PrimaryFeasibility: Retentionover 12 weeksPercentage of participants completing baseline and follow-up assessments (criteria: at least 80 percent)
PrimaryFeasibility: Safety (number/presence of intervention-related serious adverse events)over 12 weeks (intervention period)Adverse events related to intervention (criteria: no serious events)
SecondaryPhysical Functioning: 4 meter walk test (pre and post intervention (12 weeks)usual gait speed over 4 meters
SecondaryPhysical Functioning: dual-task cognitive Timed Up and Go (TUG-COG)pre and post intervention (12 weeks)time to rise from a standard chair, walk 3 meters, turn around, walk back to the chair and sit down while counting backwards by three
SecondaryPhysical Functioning: Two minute step test (TMST)pre and post intervention (12 weeks)number of steps in two minutes
SecondaryPhysical Functioning: 30-second chair stand test (30CST)pre and post intervention (12 weeks)number of full stands from a chair in 30 seconds
SecondaryPhysical Functioning: Preclinical Mobility Limitation (PCML) scalepre and post intervention (12 weeks)
classified as no mobility limitation, preclinical mobility limitation, minor manifest limitation or major manifest limitation for 3 tasks (walking 0.5km, walking 2 km, and climbing one flight of stairs)
SecondaryCognitive Functioning: California Older Adult Stroop Test (COAST)pre and post intervention (12 weeks)measures executive functioning by assessing the ability to inhibit an automatic response
SecondaryCognitive Functioning: Digit Symbol Substitution Test (DSST)pre and post intervention (12 weeks)assesses various aspects of cognition, including processing speed and several aspects of executive functioning (planning, attention, and working memory)
SecondaryCognitive Functioning: Oral Trail Making Test (OTMT)pre and post intervention (12 weeks)involves task-shifting (mental flexibility), attention, working memory and processing speed
SecondaryEnjoyment: Physical Activity Enjoyment Scale (PACES)week 1,2,4,6,8,10,12Scale 8-56 (higher score is greater enjoyment)
SecondaryAffective response to exercise: Feelings Scale (FS)week 1,2,4,6,8,10,12Scale +5 to -5 (+5 very good, -5 very bad)
SecondaryHarmsover 12 week intervention periodany intervention-related adverse events (e.g., muscle soreness, muscle strains, etc.,) reported by participants
OtherProcess Outcome: Self Efficacy for Exercise Scale (SEE)pre and post intervention (12 weeks)Scale 0-90 (higher scores is greater self-efficacy)
OtherProcess Outcome: Activities Balance Confidence (ABC) Scalepre and post intervention (12 weeks)0-100 percent, higher scores equals greater confidence

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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