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WithdrawnNCT06682013Updated May 29, 2026

Virtual Agent Feasibility in Oncology Patients (NTT Data)

An interventional study of Virtual agent and Human agent in Lung Cancer, sponsored by Duke University. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-29.

Sponsored by Duke University · Not applicable, Interventional, and Health services research

Why this study was withdrawn
Poor accrual
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

The purpose of this study is to compare the use of a virtual agent vs. a human agent when onboarding oncology patients over the telephone to Remote Patient Monitoring (RPM) devices. RPM devices are instruments that a patient can use to measure their own weight and vital signs. Both the virtual and human agents will be available by telephone to instruct the patient on how to use the RPM devices to measure weight, blood pressure, heart rate, temperature, and oxygen saturation. Patients will be randomized to either the virtual or human agent, have assessments of their medical and oncological history, overall well-being, body measurements, and vital signs, and will complete questionnaires about their experience.

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Conditions studied

  • Lung Cancer

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03

In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

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Lead sponsor

Duke University is the lead sponsor of 2,025 studies on the registry; 275 are open to participants now.

Of its 194 completed or terminated interventional studies of FDA-regulated products, 159 (82%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Willing and able to provide written informed consent and HIPAA authorization for the release of personal health information.
  2. Age ≥18
  3. Cancer (solid tumor)
  4. Planning to return to Duke Cancer Center clinic for three days in a row

    • Patients whose treatment does not require that they return to clinic for three days in a row, but who are willing to voluntarily return to participate in this study are permitted to enroll.
  5. Eastern Cooperative Oncology Group (ECOG) score of 0-2
  6. Native fluency of spoken English as determined by the investigator

    • Non-native English speakers are permitted to enroll if they have achieved native fluency.
  7. Vitals as collected by the clinic using Duke maintained equipment must be within the ranges specified by the remote patient monitoring devices.

    • Weight ≤ 180 kg
    • Systolic blood pressure ≤ 300 mmHg
    • Pulse rate of 40-200 bpm
    • SpO2 of 70-100%
    • Temperature 34.0-42.2°C
  8. Arm circumference of 22-42 cm

Exclusion criteria

Exclusion Criteria:

  1. 1. Vision, speech, auditory, physical, cognitive or other impairment that has the potential to interfere with the use of the remote patient monitoring device or agent, in the opinion of the investigator or study coordinator.
  2. Has an implanted pacemaker, arterio-venus (A-V) shunt, a history of mastectomy or lymph node clearance, history of severe blood flow problems or blood disorders, or a history of severe circulatory deficit in the arm.
  3. Is pregnant
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Virtual agent

    Device: Virtual agent

  • Active comparator
    Human agent

    Other: Human agent

Interventions

  • DeviceVirtual agent

    The virtual agent is an interactive audio agent that is similar to voice agents that interact with callers in many industries today. They create a very human-like interaction in contrast to more traditional virtual call agents that can only respond to menu options (e.g. "choose "1" for appointments, choose "2" for questions about your bill", etc.). The virtual agent is engineered to accomplish the very specific task of onboarding the patient on use of the RPM devices. It is trained to understand normal human English speech, detects emotional tone and frustration of callers, and is trained to deescalate when appropriate.

  • OtherHuman agent

    The human agent will onboard the patient on use of the RPM devices.

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What researchers measure

Primary outcomes

  1. Usability of virtual agent vs. human agent for onboarding patients to RPM devices as assessed by the System Usability Scale (SUS)

    The SUS is a questionnaire that assesses perceived usability. It includes 10 five-point items with alternating positive and negative tone. The final score is a number 0-100 with a higher score indicating better usability.

    Time frame: Day 1, Day 2, Day 3

Secondary outcomes

  1. Description of the patient experience when using a virtual agent in the context of teaching a patient as assessed by the patient experience survey.

    The patient experience survey includes 3 open-ended questions about experience with the training process, input on using monitoring devices at home, and any other important information for the researchers to know. Descriptive analysis will be conducted within each arm.

    Time frame: Day 3

  2. Identification of opportunities to improve the use of a virtual agent in the context of teaching a patient as assessed by the patient experience survey.

    The patient experience survey includes 3 open-ended questions about experience with the training process, input on using monitoring devices at home, and any other important information for the researchers to know. Descriptive analysis will be conducted within each arm.

    Time frame: Day 3

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Study locations

1 site
  • Duke University Medical Center
    Durham, North Carolina 27710, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06682013
Lead sponsor
Duke University
Responsible party
Sponsor
First posted
Nov 12, 2024
Start date
May 2026 (estimated)
Primary completion
May 2026 (estimated)
Completion
May 2026 (estimated)
Last update
May 29, 2026

Study contacts

Laura Alder, MD
principal investigator · Duke University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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