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E-Care Acceptability for Older People Undergoing Chemotherapy

Not Applicable
Withdrawn
Conditions
Cancer
Interventions
Device: CHATBOT use
Registration Number
NCT05408195
Lead Sponsor
University Hospital, Toulouse
Brief Summary

The main objective of this pilot study is to evaluate the acceptability of clinical data collection using a semi-automated e-solution based on the use of text messaging among older adults undergoing chemotherapy treatment at home.

Detailed Description

Most cancer diagnosis are made among the 70 years and over population. In this population, negative consequences of cancer treatments are of great concern, especially for those who are socially isolated or live in rural areas. International oncology societies recommend personalized treatments to reduce adverse events. However, few tools have been validated in this population to monitor compliance and risks of outpatient treatments. In addition, health professionals continue to manage unplanned patient calls which could disrupt effectiveness of their work. Our hypothesis is that the semi-automated collection of health data (text message questionnaires) during outpatient chemotherapy secures the patient's care pathway and optimizes care time, in particular for patients' education and support. Therefore, patients (and/or their caregivers) who benefit from calls follow-up (usual care), would have the possibility of receiving an additional weekly remote questionnaire (by email or SMS) via a CHATBOT on any terminal. This automated questionnaire collects data on tolerance and compliance with care plan.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Subjects of 70 years of age or older;
  • Subjects undergoing chemotherapy treatment after a cancer diagnosis;
  • Subjects managed by the oncogeriatrics team at the Toulouse University Hospital as part of an outpatient follow-up and followed by conventional telephone calls and CHATBOT support.
Exclusion Criteria
  • Patient's refusal to participate.
  • Patient does not have sufficient equipment for downloading and using the CHATBOT tool
  • Participant under guardianship, curatorship or safeguard of justice.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
CHATBOT usersCHATBOT usepatients downloading and using the CHATBOT
Primary Outcome Measures
NameTimeMethod
Acceptance of semi-automated follow-up6 months of CHATBOT use

Proportion of patients who uploaded the application, Proportion of patients who received at least one questionnaire, Proportion of patients who answered at least one questionnaire, Completion questionnaire rate and answered questionnaire rate

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CHU de Toulouse

🇫🇷

Toulouse, France

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