Evaluation of the Contribution of a DEMaterialized VIdeo-pedagogical SUpport in the Care Pathway of Lung Cancer Surgery Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: video support.
- Who it may be relevant to
- Registry conditions: Lung Cancer. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
Uni-centric, randomized, open-label, prospective interventional-comparative study, with a control arm (patients receiving standard preoperative information) and an experimental arm (patients receiving standard preoperative information and having access to a dematerialized educational video support).
Interventions
- Other video support
video support provided to the patient before surgery
Primary outcome measures
- Immediate pre-operative anxiety [Time frame: 10 days]
Secondary outcome measures (5)
- Perioperative anxiety (randomization (consultation), immediate postoperative and discharge) [Time frame: 90 days]
- Post-traumatic stress disorder [Time frame: 90 days]
- Quality of life evaluation [Time frame: 90 days]
- Cumulative postoperative morbidity [Time frame: 90 days]
- Intra-hospital consumption of analgesics [Time frame: 90 days]
Eligibility criteria
Inclusion criteria
- Patients aged 18 or over,
- Patients requiring surgical management:
for therapeutic purposes (in the case of proven tumor histology) or for diagnostic and therapeutic purposes (in the absence of proven histology, but strong suspicion, after validation by RCP),
\- Patients who have given their consent.
Exclusion criteria
- Patients under guardianship
- Patients with a history of thoracic surgery
- Patients on long-term analgesic medication
- Patients who do not speak French
- Patients unable to read or write
- Patients with major visual impairment
- Patients with chronic anxiety or depression at the time of admission
- Patients under guardianship
- Pregnant or breast-feeding women
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Prevention
Study locations
France · 1 center
- Assistance publique Hopitaux de Marseille - Hopital Nord — Marseille
Identifiers
NCT: NCT06577844 · RCAPHM22_0413