Impact in Head and Neck Oncology of Support by a Nurse in the Patient's Care Pathway

NCT ID: NCT06203808

Last Updated: 2024-04-04

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 320 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-02-20
• Study Completion Date: 2025-02-28

Brief Summary

Head and neck cancers (HNC) constitute a significant global health burden, ranking fourth in terms of cancer incidence and fifth in terms of cancer-related mortality. The management of HNC requires a complex array of consultations, examinations, rehabilitation, and lifestyle modifications, including addiction cessation. These cancers disproportionately affect economically disadvantaged, socially isolated individuals, and the elderly, resulting in disparities in healthcare access. Health coaching, an approach aimed at improving patients' health and quality of life by supporting behavior and lifestyle changes, has demonstrated effectiveness in various medical fields, including chronic diseases, medical oncology, and hematology. However, its application in head and neck cancer care remains limited, despite its potential benefits for this patient population.

Detailed Description

This study is a prospective monocentric comparative investigation conducted over 12 months. Two groups are being compared: the COACH group and the control group. The COACH group consists of newly diagnosed head and neck cancer patients seen in consultation for treatment information at University Hospital during the first two months of the study. These patients receive coaching support from a specialized nurse, facilitating appointment scheduling, treatment coordination, and access to various rehabilitation services. In contrast, the control group includes patients who received treatment information during the third and fourth months of the study, without receiving specific coaching support. Both groups of patients will complete quality of life questionnaires at the time of treatment information, at 3 months, 6 months, and at 12 months.

Hypothesis: the investigators assume a minimum difference of 5 points between the control group and the coaching group.

Conditions

Head and Neck Cancer

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

COACH GROUP

The COACH group consists of newly diagnosed head and neck cancer patients seen in consultation for treatment information at Oncologic University Hospital during the first two months of the study. These patients receive coaching support from a specialized nurse, facilitating appointment scheduling, treatment coordination, and access to various rehabilitation services

COMPLETION OF QUESTIONNAIRES

Intervention Type: OTHER

Both groups of patients will complete quality of life questionnaires at the time of treatment information, at 3 months, 6 months and at 12 months.

CONTROL GROUP

The control group includes patients who received the treatment information during the third and fourth months of the study, without receiving specific coaching support.

COMPLETION OF QUESTIONNAIRES

Intervention Type: OTHER

Both groups of patients will complete quality of life questionnaires at the time of treatment information, at 3 months, 6 months and at 12 months.

Interventions

COMPLETION OF QUESTIONNAIRES

Both groups of patients will complete quality of life questionnaires at the time of treatment information, at 3 months, 6 months and at 12 months.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patient with a histologically proven diagnosis of head and neck squamous cell carcinoma (HNSCC) of the upper aerodigestive tract
• Patient whose disease is classified UICC (Union for International Cancer Control (UICC) Tumour, Node, Metastasis (TNM) stage (8th edition): T0-4a NO/N3 M0 (no distant metastasis M0)
• Patient World Health Organization (WHO) 0-1-2
• Treatment with a feasible curative aim (no contraindication to optimal treatment such as surgery or chemotherapy at a curative dose)
• Patient affiliated to a Social Security scheme in France
• Patient who did not object to participating in the research.

• Patient with a history of previous cervical surgery and/or head and neck irradiation
• Pregnant or breastfeeding women
• Patient suffering from another co-existing malignant disease at the time of inclusion or any other significant medical (immunosuppression etc.), psychiatric or surgical condition, currently not controlled by treatment, which may interfere with the achievement of the study.
• Any psychological, family, geographic or sociological condition that does not allow compliance with medical monitoring and/or the procedures provided for in the study protocol.
• Patients deprived of liberty or under legal protection regime (curatorship and guardianship, safeguard of justice).

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Toulouse

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

AGNES DUPRET-BORIES

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Toulouse

Locations

Chu de Toulouse

Toulouse, , France

Site Status: RECRUITING

Countries

France

Central Contacts

AGNES DUPRET-BORIES

Role: CONTACT

dupretbories.a@chu-toulouse.fr

(0)5 31 15 60 14 ext. +33

MARIANNE LESCOUZERES

Role: CONTACT

lescouzeres.m@chu-toulouse.fr

Facility Contacts

AGNES DUPRET-BORIES

Role: primary

dupretbories.a@chu-toulouse.fr

(0)5 31 15 60 14 ext. +33

MARIANNE LESCOUZERES

Role: backup

lescouzeres.m@chu-toulouse.fr

Other Identifiers

RC31/23/0410

Identifier Type: -

Identifier Source: org_study_id