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Trial · NCT04445792

Outcomes12

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Individuals Identified as Potential Participants Through EHR (Electronic Health Record)Up to 3 yearsIndividuals who were prescreened.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Individuals Who Were Screened to the Acute Pain, Chronic Pain, and Depression TrialsUp to 3 yearsIndividuals who were screened for the Acute Pain, Chronic Pain, and Depression Trials.ParticipantsCOUNT_OF_PARTICIPANTS
PRIMARYNumber of Participants Who Were Randomized to the Acute Pain, Chronic Pain, and Depression TrialsUp to 3 yearsParticipants who were consented to the Acute Pain, Chronic Pain, and Depression Trials.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYPain Interference as Measured by PROMIS (Patient-Reported Outcomes Measurement Information System)6 monthsRandomized population with completed 6 month survey.T-scoreMEAN
SECONDARYPhysical Function as Measured by PROMIS (Patient-Reported Outcomes Measurement Information System)6 monthsRandomized population with completed 6 month survey.T-scoreMEAN
SECONDARYSleep Disturbance as Measured by PROMIS (Patient-Reported Outcomes Measurement Information System)6 monthsRandomized population with completed 6 month survey.T-scoreMEAN
SECONDARYAbility to Participant in Social Roles and Activities as Measured by PROMIS (Patient-Reported Outcomes Measurement Information System)6 monthsRandomized population with completed 6 month survey.T-scoreMEAN
SECONDARYFatigue as Measured by PROMIS (Patient-Reported Outcomes Measurement Information System)6 monthsRandomized population with completed 6 month survey.T-scoreMEAN
SECONDARYAnxiety as Measured by PROMIS (Patient-Reported Outcomes Measurement Information System)6 monthsRandomized population with completed 6 month survey.T-scoreMEAN
SECONDARYDepression as Measured by PROMIS (Patient-Reported Outcomes Measurement Information System)6 monthsRandomized population with completed 6 month survey.T-scoreMEAN
SECONDARYOverall Wellbeing as Measured by PROMIS (Patient-Reported Outcomes Measurement Information System)6 monthsRandomized population with completed 6 month survey.score on a scaleMEAN
SECONDARYNumber of Participants With Pharmacogenetic Drug-Gene Concordance10 days for Acute Pain; 3 months for Chronic Pain and DepressionRandomized population with completed 6 month survey.ParticipantsCOUNT_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.

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