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RecruitingNCT06577844ClinicalTrials.gov record

Evaluation of the Contribution of a DEMaterialized VIdeo-pedagogical SUpport in the Care Pathway of Lung Cancer Surgery Patients

Lung Cancer

THE QUICK READ

What this study involves

The registry says this study is recruiting. Individual locations may have different availability.

Study type
Interventional
Phase
Not applicable
Age range
18 years - Not specified
Sex eligible
All sexes
Healthy volunteers
Not accepted
Participants
226 Estimated

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

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).

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

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
Understand screening

Treatment, groups and participation

The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.

Assignment
Random assignment
Masking
No masking
experimental

Not reported in this registry record.

Other: video support

control

Not reported in this registry record.

video support OTHER

video support provided to the patient before surgery

Prepare your questions

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Immediate pre-operative anxiety

Time frame: 10 days

self-measurement using the HAD Scale

Secondary measures

Perioperative anxiety (randomization (consultation), immediate postoperative and discharge)

Time frame: 90 days

based on HAD scale

Post-traumatic stress disorder

Time frame: 90 days

PCL-5 scale

Quality of life evaluation

Time frame: 90 days

European Organisation for Research and Treatment of Cancer core health- related quality of life questionnaire (QLQ-C30).

Cumulative postoperative morbidity

Time frame: 90 days

score CCI

Intra-hospital consumption of analgesics

Time frame: 90 days

accounting for in-hospital consumption of analgesics

No results are flagged as posted.

Review the complete result tables and limitations in the official record.

Open official results ↗

Research locations (1)

The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.

1 locations

Assistance publique Hopitaux de Marseille - Hopital NordMarseille, France, FranceRecruiting
Alex Fourdrain, MD, PhDCONTACTalex.fourdrain@ap-hm.fr+33 4 91 96 43 95
Alex Fourdrain, Md, PhDPRINCIPAL_INVESTIGATOR
View location on map ↗

Study team and timeline

Lead sponsor
Assistance Publique Hopitaux De Marseille
Study start
Jul 11, 2024 Actual
Primary completion
Jan 11, 2028 Estimated
Study completion
Apr 11, 2028 Estimated
First posted
Aug 29, 2024 Actual
Last updated
Nov 10, 2026 Actual

Official study contacts

Official study title

Evaluation of the Contribution of a DEMaterialized VIdeo-pedagogical SUpport in the Care Pathway of Lung Cancer Surgery Patients

A HUMAN NEXT STEP

Ask Wellness Clinical Research

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Sending a question does not enroll you in a trial.

Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.

Retrieved: Nov 12, 2026 · Last registry update: Nov 10, 2026