Criteria Associated With Patient Willingness to Participate in Biomedical Research

University Hospital, Montpellier1,000 enrolled

Overview

The primary objective of this study is to determine the variables associated with patient acceptation or refusal to participate in a clinical research protocol when seen in during a pneumology consultation (excluding oncology and tobaccology).

The secondary objectives of this study are: * To compare patient acceptance rates for participation in a clinical research protocol before and after January 15, 2016. * To determine the variables associated with accepting or refusing to participate in a clinical research protocol for patients seen during a pneumology consultation (excluding oncology and tobaccology) before January 15, 2016. * To determine the variables associated with accepting or refusing to participate in a clinical research protocol for patients seen during a pneumology consultation (excluding oncology and tobaccology) after January 15, 2016. * To describe the patient population seen during pneumology consultations. * To determine the variables associated with accepting or refusing to participate in a clinical research protocol sponsored by a pharmaceutical laboratory. * To determine the variables associated with accepting or refusing to participate in a clinical research protocol sponsored by an academic institution. * Construct clusters (homogeneous groups) of patients seen during the pneumology consultations.

Study Type

OBSERVATIONAL

Enrollment

1,000

Conditions

Consulting in Pneumology Department, But Not for Oncology or Tobacology

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * The patient was informed about the study. * The patient is scheduled for a consult in the pneumology department Exclusion Criteria: * The patient is under judicial protection or is an adult under any kind of guardianship * The patient expresses opposition to the study * It is impossible to correctly inform the patient about the study * The patient cannot fluently read French * The patient is pregnant * The patient is breastfeeding * The patient has cancer * The patient is consulting in tabaccology

Locations (4)

Polyclinique Saint-Privat

Boujan-sur-Libron, France

Clinique de Marignane

Marignane, France

APHM - Hôpital Nord

Marseille, France

Centre Hospitalier Universitaire de Montpellier

Montpellier, France

Outcomes

Primary Outcomes

Acceptation or refusal to participate in a biomedical research study

Positive or negative response to the question "If a biomedical research protocole were proposed to you, would you accept to participate?"

Time frame: Day 0 (cross-sectional study)

Secondary Outcomes

The PROTOACCEPT questionnaire

The PROTOACCEPT questionnaire (see links below).

Time frame: Day 0 (cross-sectional study)

Data from ClinicalTrials.gov

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