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Alter-EgoNCT07572838

Alter-Ego as an Assistive Robotic Device.

StatusCompleted
PhaseNot specified
Primary completion
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Record History

All 2 versions: 2 with changes below. See every version on ClinicalTrials.gov ↗

  1. Notable Primary endpoint(s) modified Show 6 more changesShow less
    • Completed without a posted recruiting period
    • Primary completion date changed from estimate of Aug 2026 to Oct 15, 2026
    • Start date changed from estimate of May 2026 to Jun 1, 2026
    • Eligibility criteria expanded, about 17 words
    • Study description expanded, about 406 words
    • Site contact updated
  2. Study First Submitted
  • Notable: the plan changed

Endpoints

Primary

The SUS (System Usability Scale) assessment is conducted after each experimental session.
Timeframe: up to 24 weeks
The QUIS (Questionnaire for User Interaction Satisfaction) assessment is conducted after each experimental session.
Timeframe: up to 24 weeks
The NASA RTLX (NASA Raw Task Load Index) assessment is conducted after each experimental session.
Timeframe: up to 24 weeks
Change in perception of the robot (pre vs post interaction)
Timeframe: up to 24 weeks
Participants' subjective experience of interaction with Alter-Ego (qualitative)
Timeframe: up to 24 weeks

Arms and interventions

ALS patient
Healthcare Professionals

Sites

1 site in 1 country

  • Istituti Clinici Scientifici Maugeri IRCCS, Milan InstituteMilan, Milan, Italy