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Trial · NCT07434934

Registered outcomes20

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

ListOutcomeTime frameDescription
PrimaryGait Velocity- single-task (BTS GAITLAB)six weeks
Measured using BTS GAITLAB (Physiotherapy Laboratory, University of Sharjah) during walking under single-task condition (walking only). Report mean gait velocity across trials. Higher = faster walking.
PrimaryGait velocity during dual-task walking (m/s)6 weeksMeasured using BTS GAITLAB during walking under dual-task cognitive condition. Report mean gait velocity across trials. Higher = faster walking under dual-task.
SecondaryBalance - Berg Balance Scale (BBS)Six weeksBalance assessed using the Berg Balance Scale. Report total score (0-56). Higher = better balance.
SecondaryActivities-specific Balance Confidence (ABC) Scale score (0-100%)6 weeksBalance confidence assessed using the ABC scale. Report total/mean percentage score (0-100%). Higher = greater confidence.
SecondaryFive Times Sit-to-Stand test time (seconds)6 weeksFunctional lower-limb performance assessed using five times chair sit-to-stand test. Report completion time in seconds. Lower = better.
SecondaryFunctional Mobility Scale (FMS) rating6 weeksFunctional mobility assessed using the Functional Mobility Scale. Report FMS rating (per standard scoring). Higher = better mobility.
SecondaryBiodex Balance System stability index (unit per device output)6 weeks
Instrumented balance assessed using the Biodex Medical Balance System (Physiotherapy Laboratory, University of Sharjah). Report stability index as provided by the device. Interpret direction as per device metric (lower = better stability).
SecondaryDaily step count measured by FIBION (steps/day)6 weeksPhysical activity assessed using FIBION activity monitor worn 7 consecutive days / 24 h before and after intervention. Report mean daily step count over the monitoring period. Higher = more activity.
SecondaryModified Physical Activity Scale (M-PAS) score6 weeksSelf-reported physical activity assessed using M-PAS. Report total score (per instrument scoring). Specify direction per scoring (higher = more activity).
SecondaryFalls Efficacy Scale-International (FES-I) total score6 weeksFall concern assessed using FES-I. Report total score (per instrument scoring). Higher = greater concern about falling (worse).
SecondaryModified Fatigue Impact Scale (MFIS) total score6 weeksFatigue assessed using MFIS. Report total score (per instrument scoring). Higher = worse fatigue impact.
SecondaryShort Form-36 (SF-36) health-related quality of life score6 weeksQuality of life assessed using SF-36. Report domain scores and/or Physical and Mental Component Summary scores (per SF-36 scoring). Higher = better health status.
SecondaryHospital Anxiety and Depression Scale (HADS-A) score (0-21)6 weeksAnxiety symptoms assessed using HADS Anxiety subscale. Report subscale score (0-21). Higher = worse anxiety symptoms.
SecondaryHospital Anxiety and Depression Scale (HADS-D) score (0-21)6 weeksDepressive symptoms assessed using HADS Depression subscale. Report subscale score (0-21). Higher = worse depressive symptoms.
Secondary6-Minute Walk Test distance (meters)6 weeksPhysical performance assessed using the 6-minute walking test. Report distance walked in meters. Higher = better walking endurance.
SecondaryMontreal Cognitive Assessment (MoCA) total score (0-30)6 weeksGlobal cognitive function assessed using the MoCA. Report total score (0-30). Higher = better cognition.
SecondarySymbol Digit Modalities Test (SDMT) score (correct responses)6 weeksProcessing speed assessed using SDMT (BICAMS component). Report total correct responses (per scoring). Higher = better.
SecondaryHopkins Verbal Learning Test-II (HVLT-II) total recall score6 weeksVerbal learning/memory assessed using HVLT-II (BICAMS component). Report total recall score (per scoring). Higher = better.
SecondaryBrief Visuospatial Memory Test-Revised (BVMT-R) total recall score6 weeksVisuospatial memory assessed using BVMT-R (BICAMS). Report total recall score (per scoring). Higher = better memory.
SecondaryStroop test interference score (per protocol)6 weeksInhibitory control assessed using the Stroop test. Report interference score. lower interference score = better

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

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.

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