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Trial · NCT05946551

Outcomes20

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants That Had Any Confusion Over How to Take the Study Drug, Including Which Pill to Take, When to Take it, or How Many to TakeEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants That Had Trouble Adhering to the Study Drug ScheduleEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants That Had Any Difficulty Using the REDCap Interface.End of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants That Prefer Participating in This Virtual StudyEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants Satisfied With Their Opportunities to Interact With Study StaffEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants That Felt They Could Reach Study Staff if NeededEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants That Felt That Study Staff Was Available and Easy to Contact to Report Any Adverse EffectsEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants That Felt That the Amount of Information Collected in Each Series of Surveys Was AcceptableEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants That Felt That the Frequency in Which the Information Was Collected Was AcceptableEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYImprovement RatingEnd of the Treatment Phase at 12 weeksScore on a scaleMEAN
PRIMARYQuality of Life (QoL) Score RatingEnd of the Treatment Phase at 12 weeksScore on a scaleMEAN
PRIMARYInterest ScoreEnd of the Treatment Phase at 12 weeksscore on a scaleMEAN
SECONDARYProportion of Survey CompletionEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProportion of Study Drug AdherenceEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProportion of Lost to Follow Up (LFUP)End of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProportion of Voluntary TerminationEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYAdverse Events (AEs) IncidenceEnd of the Treatment Phase at 12 weeksnumber of adverse eventsMEAN
SECONDARYSerious, Unexpected Suspected Adverse Reactions (SUSAR) IncidenceEnd of the Treatment Phase at 12 weeksNumber of SUSARsNUMBER
SECONDARYStudy-wide Serious Adverse Events (SAEs) IncidenceEnd of the Treatment Phase at 12 weeksNumber of SAEsNUMBER
SECONDARYNumber of Discontinuations or Temporary Suspensions of IPEnd of the Treatment Phase at 12 weeksParticipantsCOUNT_OF_PARTICIPANTS

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.

For software

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT05946551/outcomes