Feasibility Study of a Transition Pathway at Discharge From Full Hospitalization in Oncology

ConditionCancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de Nīmes

About this trial

Patient reported outcomes (PRO) measure the health status directly reported by the patients, without external interpretation, generally collected using self-questionnaires, including online tools (ePRO). This approach is useful in early detection of signs of relapse, with reduced anxiety, improved quality of life and survival, and reduced readmissions to emergency departments in patients with advanced cancer. In the current context where hospitalization is increasingly short, the transition from hospital to home is a critical moment that poses a significant safety challenge Patient follow-up strategies help patients return home, particularly in surgery, with telephone calls from a nurse the day after or several days after discharge. In oncology, telephone calls from the pharmacist 3 days after discharge from hospital helped to identify undesirable effects of treatments. In general medicine, these calls have led to improved patient satisfaction, reduced use of emergency departments and the resolution of drug-related problems, but are costly. The introduction of post-hospitalization ePRO monitoring in oncology could ensure effective follow-up while keeping costs under control. A coordinating nurse could manage this process and play a crucial role in accompanying patients when they return home.

The study authors aimed to evaluate the feasibility of a transitional nurse consultation and ePRO follow-up on discharge from full hospitalization in oncology in this population of frail and elderly patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

The patient must have given their free and informed consent and signed the consent form

The patient must be a member or beneficiary of a health insurance plan

Adult patient hospitalized in an oncology unit for at least 48 hours.

Patient capable of using a connected device, in possession of a smartphone or tablet, and with an internet connection at home.

Disqualifiers

The patient is in a period of exclusion determined by a previous study

The subject refuses to sign the consent

It is impossible to give the subject informed information

The patient is under safeguard of justice or state guardianship

Trial population

Consecutive patients treated as inpatients in the Medical Oncology Department of Nîmes University Hospital and scheduled to be discharged and returned home.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • OncoCare transition program

    Other intervention

    Interview with the coordinating nurse who reviews the patient's prescriptions and appointments, installs the electronic patient-reported outcome (ePRO) application on the patient's smartphone and explains collection of any symptoms. ePRO symptom monitoring by the patient on D2, D7 and D15 after discharge. The coordinating nurse phones the patient on D7 to review the symptoms reported, assess compliance with treatment and provide support. In the event of grade ≥ 2 symptoms, the nurse contacts the patient for further information and informs the referring oncologist, who decides on the course of treatment.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Compliance with ePRO monitoring

Percentage of patients who responded to all questionnaires

Time frame
Day 2
2

Compliance with the telephone call at day 7

Percentage of patients successfully contacted at day 7

Time frame
Day 7
3

Patient satisfaction with the care pathway

Question: "Are you satisfied with your care pathway?" (Yes/no)

Time frame
Day 15

Secondary outcomes

1

Quality of the transition pathway to home

Care Transitions Measure (CTM-3) questionnaire, where a 10-point increase reduces the risk of readmission by 14%

Time frame
Day 15
2

Quality of life as reported by the patient

EORTC QLQ-C30 questionnaire: The score for each subscale ranges from 0 to 100and good quality of life is associated with a high score on the functional scales and a low score on the symptom scales.

Time frame
Day 0
3

Quality of life as reported by the patient

EORTC QLQ-C30 questionnaire: The score for each subscale ranges from 0 to 100and good quality of life is associated with a high score on the functional scales and a low score on the symptom scales.

Time frame
Day 7
4

Quality of life as reported by the patient

EORTC QLQ-C30 questionnaire: The score for each subscale ranges from 0 to 100and good quality of life is associated with a high score on the functional scales and a low score on the symptom scales.

Time frame
Day 15

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.