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Trial · NCT04562987

Registered outcomes14

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

ListOutcomeTime frameDescription
Primaryintervention attendance1 month post-chemotherapycompletion of telecoaching sessions
PrimaryParticipant satisfaction: survey1 month post-chemotherapyusability survey
Primaryrecruitment yieldBaselinenumber of women who enroll compared to the number of contacts of eligible women required to obtain target sample size
Primaryretention1 month post-chemotherapyproportion of participants providing post-intervention data
Primaryacceptability of intervention: in-depth interview1 month post-chemotherapyin-depth interview to gather participant perceptions on the acceptability and usefulness of the mobile app features
SecondaryChange in Stroop task performanceBaseline, 1 month post-chemotherapyInterference score on Stroop task
SecondaryChange in Task-Switch task performanceBaseline, 1 month post-chemotherapyReaction time on Task-Switch
SecondaryChange in Trails task performanceBaseline, 1 month post-chemotherapyCompletion time of Trails
SecondaryChange in N-Back task performanceBaseline, 1 month post-chemotherapyCorrect responses on N-back
SecondaryChange in Spatial Working Memory task performanceBaseline, 1 month post-chemotherapyCorrect responses on Spatial Working Memory task
SecondaryChange in Auditory Verbal Learning Task (AVLT) performanceBaseline, 1 month post-chemotherapyTotal numbered recalled on AVLT
SecondaryChange in objective physical activity behaviorBaseline, 1 month post-chemotherapyObjective activity behavior (average minutes of physical activity per day) will be measured using actigraphy.
OtherChange in cancer-related FatigueBaseline, 1 month post-chemotherapy
The Functional Assessment in Chronic Illness Therapy (FACIT) - Fatigue Scale will be used to measure cancer-related fatigue. Scores range from 0-52, with higher scores indicating less cancer-related fatigue.
OtherMomentary symptoms14 days 4 times per day at each of the following time points: baseline, mid-intervention (2-3 months from baseline), 1 month post-chemotherapyA brief ecological momentary assessment prompted to participants' smartphones will be used to measure momentary symptoms, including anxiety, stress, fatigue, focus, pain, and nausea.

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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GET https://conductscience.org/api/trials/v1/NCT04562987/registered