Breast Cancer Survivor (BCS) Study

syn69968723

Created By Jessica Malenfant jmalenfant

sex: Female
grant: R03CA191712
years: 2015 2016
gender: Female
Methods: syn74497804
endYear: 2016
studyID: STUDY_BCS
ageGroup: Adults (18-64)
irbScope: Primary study
Variables: syn75072058
startYear: 2015
studyName: The Breast Cancer Survivor Study (BCS)
ackContent: syn68988177/wiki/640076
studyWaves: Pilot
Instruments: syn75072123
burstDesign: Single-burst pilot study
burstLength: days
contentType: study
dataTypeAll: Protocol Code Book Survey
institution: University of South Florida Stony Brook University
measureType: Questionnaire / Survey
sexEligible: Female
diseaseFocus: Condition-Focused Populations
metadataType: study
enrollmentAge: 40-64
exclusionTags: Neurological comorbidity excluded Cognitive impairment excluded
inclusionTags: Diagnosis required Sex-based eligibility Treatment/medication status required
studyMetadata: syn68988177/wiki/635580
RelatedStudies:
burstFrequency: One-time
metadataStatus: Available
numberOfBursts: 1
populationType: Clinical Population
recruimentWave: Pilot
Acknowledgement: syn76374423
constructDomain: Mental Heath & Emotional Functioning Cognitive Physical Health & Lifestyle Developmental & Functional Clinical & Medical History Environmental & Contextual
dataContributor: Stony Brook University
promptFrequency: 5 times per day
sexDistribution: 100% Female
burstLengthValue: 14
raceDistribution: 79% White 15% Black 4% Asian 2% Another race
studyDescription: This study examines how breast cancer survivors’ cognitive functioning in daily life compares to traditional lab-based assessments, using smartphone-based tasks and daily reports over two weeks. It also investigates whether day-to-day fluctuations in fatigue, mood, and stress predict changes in cognitive performance.
temporalCoverage: 2015-2016
measuredConstruct: Affect / Mood General Health Status Psychological Well-being Anxiety Stress Emotional Regulation Cognition Executive Function Memory Sleep Fatigue Pain Physical Activity Daily Living Skills Clinical History Demographics
totalParticipants: 47
AccessRequirements: syn77442134
administrationMode: Self-administered
genderDistribution: 100% Female
methodsDescription: syn74497804
primaryHealthFocus: Condition-Focused
selectionIntensity: Highly Selective
collectionModality : Mixed
enrollmentTimepoint: baseline
protocolDescription:
ascertainmentContext: Clinic-ascertained
populationDescriptor: Survivors of recent breast cancer, stages I and II
administrationContext: institutional laboratory, followed by ecological momentary assessment
ethnicityDistribution: 13% Hispanic or Latino
metadataCoverageNotes: Some measures not shareable due to HIPAA
metadataCoverageScope: Shareable-only
principalInvestigator: Stacey Scott Brent Small
promptingScheduleType: Quasi-random
hasObservationTimestamp: true
criteriaSelectionIntensity: Highly-Selective
eligibilityCriteriaSummary: Specific eligibility criteria include: a) be women 40-65 years of age; b) have no documented or observable psychiatric or neurological disorders that would interfere with study participation (e.g., dementia, psychosis); c) be capable of speaking and reading standard English; d) have no history of cancer other than breast cancer or basal cell skin carcinoma; e) have been treated for stage 0, 1 or 2 breast cancer at the Moffitt Cancer Center (MCC) with a minimum of four cycles of chemotherapy; f) have completed treatment between 6 and 36 months previously; g) have no recurrence of breast cancer; and h) provide written informed consent
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