CLINICAL_TRIALS ClinicalTrials.gov record update

Randomized Clinical Trial of FitBit and Mobile Apps Versus Usual Care to Improve Post-Operative Outcomes After GI Cancer Surgery

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT03623464
Title field or adapter rule: {'original_value': 'Randomized Clinical Trial of FitBit and Mobile Apps Versus Usual Care to Improve Post-Operative Outcomes After GI Cancer Surgery', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At: 2026-10-31T23:27:24.815447+00:00
Published At: 2026-09-28T00:00:00+00:00
Record Updated At: 2026-09-28
Source Retrieved At: 2026-10-31T22:17:54.613222+00:00
Timestamp Basis: ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
Date limitation: ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

protocolSection.conditionsModule.conditions: ["Pancreatic Cancer", "Gastric Cancer", "Hepatic Cancer", "Colon Cancer", "Rectal Cancer", "Small Bowel Cancer"]
protocolSection.statusModule.lastUpdatePostDateStruct: {"date": "2026-09-28", "type": "ACTUAL"}
protocolSection.identificationModule.nctId: "NCT03623464"
protocolSection.identificationModule.officialTitle: "Randomized Clinical Trial of FitBit and Mobile Apps Versus Usual Care to Improve Post-Operative Outcomes After GI Cancer Surgery"
protocolSection.statusModule.overallStatus: "SUSPENDED"
protocolSection.designModule.phases: ["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct: null

{'armGroupLabels': ['Mobile app and Fitbit + Standard of care'], 'description': "Mobility data will be generated using a mobile health tracker designed for smartphone devices, which allows the phone to automatically and passively (no patient input needed) capture information on the patient's activity; i.e. if the person is walking, remaining stationary, or moving at a rapid speed (eg. in a car). The app will prompt patients once daily to answer a series of questions that will collect patient reported symptoms and health status data. Physicians will be alerted to abnormal values within 24-48 hours and patients will be triggered to call their physicians immediately if the values are outside of normal parameters.", 'name': 'Mobile health application and Fitbit + standard of care', 'type': 'OTHER'} (protocolSection.armsInterventionsModule.interventions[])
{'armGroupLabels': ['Standard of care'], 'description': 'Post-operative standard of care information', 'name': 'Standard of care', 'type': 'OTHER'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

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