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Criteria Associated With Patient Willingness to Participate in Biomedical Research (PROTOACCEPT)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Completed

Conditions

Consulting in Pneumology Department, But Not for Oncology or Tobacology

Study type

Observational

Funder types

Other

Identifiers

NCT03098303
9373
2014-A01201-46 (Other Identifier)

Details and patient eligibility

About

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).

Full description

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.

Enrollment

1,000 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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