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Trial · NCT06404099

Registered outcomes15

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

ListOutcomeTime frameDescription
PrimaryChange in total score of the PROMIS 8a SRI to assess sleep-related impairmentBaseline, End of Intervention (Day 77)
The PROMIS 8a SRI form includes a total of 8 items that ask participants to reflect on their sleep-related daytime impairment over the past 7 days with questions rated not at all to very much. T-Scores range from 0 to 100, with a score of 55 being 1 standard deviation above population mean. Higher scores indicate greater sleep-related impairment.
SecondaryChange in total score of the PROMIS 8b SD to assess sleep disturbanceBaseline, End of Intervention (Day 77)
The PROMIS 8b SD form includes a total of 8 items that ask participants to reflect on their sleep over the past 7 days with one question rated very poor to very good and the remaining questions rated not at all to very much. T-Scores range from 0 to 100, with \> 55 1 SD above population mean.
SecondaryChange in PROMIS 10a Fatigue scoreBaseline, End of Intervention (Day 77)The PROMIS 10a Fatigue is a 10-item questionnaire that assesses a participant's fatigue on a scale of 1 (not at all fatigued) to 5 (very much).
SecondaryChange in an objective neurocognitive battery scoreBaseline, End of Intervention (Day 77)
SecondaryChange in ECog2 measureBaseline, End of Intervention (Day 77)
Everyday Cognition 2 (ECog2) is a self-report, 41-item questionnaire used to measure measure the participant's perceived capacity to perform activities related to cognitive function, which could impact major activities of daily living and independence. It has been used for patients with mild cognitive impairment, Alzheimer's Disease, and dementia. It takes 5 minutes to complete.
SecondaryChange in PASC Symptom Questionnaire responsesBaseline, End of Intervention (Day 77)
Participants will be asked to complete a questionnaire that asks about the presence of PASC symptoms at Baseline and at follow-up visits. This questionnaire includes symptoms that have been associated with PASC.
SecondaryChange in total score on the Insomnia Severity Index (ISI)Baseline, End of Intervention (Day 77)
The ISI is a 7-item, self-report questionnaire that assesses the nature, severity, and impact of insomnia, on a 5-point Likert scale (eg, 0 = not at all, 4 = extremely; scores: from 0 to 28). The ISI asks patients to recall their insomnia symptoms over the past 2 weeks.
SecondaryChange in within-person variability (over a 7-day period) in sleep onset time, assessed by sleep diaryBaseline, End of Intervention (Day 77)Sleep onset time will be assessed by sleep diary
SecondaryChange in average (over a 7-day period) nocturnal sleep duration, assessed by sleep diaryBaseline, End of Intervention (Day 77)Nocturnal sleep duration will be assessed by sleep diary
SecondaryChange in average (over a 7-day period) 24-hour sleep duration, assessed by sleep diaryBaseline, End of Intervention (Day 77)24-hour sleep duration will be assessed by sleep diary
SecondaryChange in average (over a 7-day period) sleep midpoint, assessed by sleep diaryBaseline, End of Intervention (Day 77)Sleep midpoint is the time half way between start and end of sleep, as assessed by sleep diary
SecondaryChange in average (over a 7-day period) nocturnal sleep duration, assessed by activity trackerBaseline, End of Intervention (Day 77)Nocturnal sleep duration will be assessed by activity tracker
SecondaryChange in average (over a 7-day period) 24-hour sleep duration, assessed by activity trackerBaseline, End of Intervention (Day 77)24-hour sleep duration will be assessed by activity tracker
SecondaryChange in average (over a 7-day period) sleep efficiency, assessed by activity trackerBaseline, End of Intervention (Day 77)Sleep Efficiency is the percentage of the sleep period spent asleep, as measured by activity tracker
SecondaryChange in average (over a 7-day period) sleep midpoint, assessed by activity trackerBaseline, End of Intervention (Day 77)Sleep midpoint is the time half way between start and end of sleep, as assessed by sleep diary

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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