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Trial · NCT07897331

Registered outcomes24

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

ListOutcomeTime frameDescription
SecondaryProportion of valid wear time in the rest stress stateFirst 48 hours after cesarean delivery
Percentage of valid minutes in which the wrist-worn wearable (Garmin Vivosmart 5) recorded a stress score of 0-25 (rest state on the device's proprietary 0-100 scale), exported via the Fitrockr platform.
SecondaryNumber of stress episodes per 24 hoursFirst 48 hours after cesarean delivery
Number of episodes of at least 3 consecutive minutes with a device-derived stress score above 50 (medium or high stress on the Garmin Vivosmart 5 proprietary 0-100 scale), exported via the Fitrockr platform and normalized to episodes per 24 hours of valid wear time.
SecondaryMedian stress recovery time after stress episodesFirst 48 hours after cesarean delivery
Median time in minutes from the end of each stress episode (at least 3 consecutive minutes with a device-derived stress score above 50) to the first subsequent minute with a stress score of 25 or below (rest state), computed from minute-level Garmin Vivosmart 5 stress scores exported via the Fitrockr platform.
SecondaryOvernight Body Battery chargeFirst and second postoperative nights (within 48 hours after cesarean delivery)
Change in the device-derived Body Battery energy score (Garmin Vivosmart 5; proprietary 0-100 scale estimated from heart rate variability, stress, sleep and activity) from the start to the end of the main nocturnal sleep period detected by the device, exported via the Fitrockr platform. Reported as score units on a 0-100 scale; positive values indicate recharge.

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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GET https://conductscience.org/api/trials/v1/NCT07897331/registered?page=2