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Starting soon Not applicable

The Research of French PaRole OncO : A Peer Supported Program for Cancer Patients

NCT06817655 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-03-15
Last updated
2025-02-10

Condition(s) studied

Cancer

Investigational drug(s) / intervention(s)

PaRole OncO France : Individual peer support

PaRole OncO France : Individual peer support: Following the development of the peer support program "PaRole OncO France", we are now proceeding with its implementation and evaluation through a pilot study. This study aims to derive both implementation-related and clinically relevant results. Prior to their assignment, all peer helpers undergo a comprehensive training course to ensure they are well-equipped for their role. Patients receive individual peer support during their treatment visits, providing real-time assistance and support within the clinical setting. The study incorporates three key measurement time points: 1. Baseline measurement (before the intervention) 2. After the intervention 3. Follow-up measurement (1months after the first intervention) 4. Follow-up measurement (6 months after the first intervention) At each time points, participants will complete a set of standardized questionnaires. These instruments are designed to capture relevant outcomes and experiences related to the peer support intervention.

Study summary

Peer support is a valuable mode of accompaniment between individuals who are facing or have faced similar challenging life experiences. In this context, a patient advisor (PA) shares their experiential knowledge, derived from living with a disease, to offer emotional, experiential, and informational support to other patients. This PA intervention represents an innovative form of support for oncology patients, potentially addressing their needs more comprehensively throughout the care pathway by integrating psychosocial dimensions into the support approach.

The present pilot study aims to investigate the implementation and effectiveness of the peer-to-peer support program "PaRole OncO France" in the oncology setting. The study will focus on:

1. Evaluating clinical and psychosocial parameters
2. Utilizing an in-depth multiple case study approach This research seeks to provide insights into how peer support can enhance the overall care experience for oncology patients, potentially leading to improved patient outcomes and a more holistic approach to cancer care.

Eligibility

Sex
ALL
Min age
15 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient participants : * Patients with newly diagnosed or recurrent cancer (urological, digestive, mammary, pulmonary, ORL, peritoneal carcinosis, melanoma, oncohaematology) * French-speaking patients * Patients adivsors : * Patient advisors will be past cancer patients not currently undergoing treatment for their cancer, and considered without evidence of disease * French-speaking patients Exclusion Criteria: * Patients participants : * Not followed in one of the participating units * Persons deprived of their liberty by judicial or administrative decision * Persons not affiliated to a social security scheme or beneficiaries of a similar scheme * Patient advisors : * Recurrence of the disease * Currently undergoing treatment for active cancer

Primary outcome measure(s)

  • Feasibility of implementation of the Peer Support Program in Oncology — 30 months
    Acceptability of PH intervention by patients, professionals, and PAs Number of PHs integrated per unit Maintenance of PH activity during the study period in each unit Primary outcome measure is multidimensional by design, as the evaluation of a peer support program requires simultaneous analysis of complementary aspects (acceptability, feasibility, fidelity). These elements are inherently interconnected within our methodological framework.

Trial sites (2)

FacilityCityRegionStatus
Hospices Civils de Lyon Lyon France
Hospices Civils de Lyon Lyon France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06817655 on ClinicalTrials.gov ↗ ← All trials in France