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NCT05318027Active, not recruitingPhase 2

ChatBot and Activity Monitoring in Patients Undergoing Chemoradiotherapy

Use of Natural Language Processing ChatBot and Automated Continuous Activity Monitoring Via Mobile Phones for Early Detection and Management of Symptoms in Patients Undergoing Cancer Treatment

Source: ClinicalTrials.gov · Last updated 1 Apr 2026

Brief summary (registry, in English)

Evaluate the feasibility of using a chatbot combined with continuous activity monitoring to proactively identify, appropriately triage and help manage patients' symptoms during cancer treatment Determine whether such an early outpatient clinic-based intervention can decrease rates of excess triage visits Correlate changes in activity and early symptom management to emergency department visits, unplanned inpatient hospitalizations and treatment breaks

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
70 (estimated)
First submitted
6 Dec 2021
Start date
22 May 2023
Primary completion date
Dec 2026
Lead sponsor
Abramson Cancer Center at Penn Medicine
NCT number
NCT05318027

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 70
  • From 22 May 2023 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients who are bed bound at baseline (ECOG 4)
  • Patients who rely on a wheelchair for ambulation

Who the study is looking for

  • Adults (age \>18 years) with a diagnosis of a head and neck, lung, gastrointestinal cancer, that are receiving concurrent chemotherapy and radiation treatment.
  • Possession of a mobile device that can receive SMS texts and can deliver FitBit data wirelessly
  • Ability read and respond in English
  • Ability to provide informed consent to participate in the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Abramson Cancer Center of the University of Pennsylvania
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.