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Improving Therapeutic Adherence With a Co-constructed Program Involving Both Patients and Health Care Professionals

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Enrolling

Conditions

Cystic Fibrosis

Treatments

Other: " Information-Motivation-Behavioral skills " intervention.

Study type

Interventional

Funder types

Other

Identifiers

NCT03226795
69HCL17_0279

Details and patient eligibility

About

Background Cystic fibrosis is a life-threatening genetic disorder responsible for pulmonary failure and multi-systemic complications involving specific and large medical care burden. To date, no program has shown its effectiveness in improving therapeutic adherence. A new approach to develop a co-constructed program involving patients and professionals may contribute to improve therapeutic adherence.

Objectives The aim of the MUCOBS-Trial project is to create a program to increase therapeutic adherence and to evaluate its efficacy in adult patients with cystic fibrosis in 3 CF centers in France.

Enrollment

450 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with Cystic Fibrosis
  • Aged 18 or more
  • Speaking / understanding French
  • Followed in one of the participating centers (CRCM of the Auvergne-Rhône-Alpes region)
  • Resident in Auvergne-Rhône-Alpes
  • Affiliated to the general health insurance scheme

Exclusion criteria

  • Transplanted Patients
  • Patients who participated in the working group for the co-construction of the intervention

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

450 participants in 1 patient group

interventional arm
Experimental group
Treatment:
Other: " Information-Motivation-Behavioral skills " intervention.

Trial contacts and locations

3

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Central trial contact

Marie Viprey; Quitterie REYNAUD

Data sourced from clinicaltrials.gov

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